geneid | 11052 |
---|---|
ensemblid | ENSG00000111605.18 |
hgncid | 13871 |
symbol | CPSF6 |
name | cleavage and polyadenylation specific factor 6 |
refseq_nuc | NM_007007.3 |
refseq_prot | NP_008938.2 |
ensembl_nuc | ENST00000435070.7 |
ensembl_prot | ENSP00000391774.2 |
mane_status | MANE Select |
chr | chr12 |
start | 69239569 |
end | 69274358 |
strand | + |
ver | v1.2 |
region | chr12:69239569-69274358 |
region5000 | chr12:69234569-69279358 |
regionname0 | CPSF6_chr12_69239569_69274358 |
regionname5000 | CPSF6_chr12_69234569_69279358 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 551 | 392 | 82 | 70 | 190 | 12 | 36 | 144 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1656 | 234 | 47 | 44 | 110 | 10 | 22 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
c0002 | 0/1 | 1656 | 151 | 33 | 25 | 77 | 1 | 14 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
c0003 | 0/0 | 1656 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
c0004 | 0/0 | 1656 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
c0005 | 0/0 | 1656 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
c0006 | 0/0 | 1656 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 4933 | 68 | 15 | 19 | 24 | 0 | 9 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0002 | 1/0 | 4929 | 52 | 6 | 11 | 31 | 1 | 2 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0003 | 0/0 | 4938 | 31 | 0 | 6 | 17 | 1 | 7 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0004 | 0/0 | 4934 | 29 | 0 | 0 | 28 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0005 | 0/0 | 4934 | 17 | 1 | 8 | 4 | 2 | 2 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0006 | 0/0 | 4935 | 14 | 3 | 0 | 11 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0007 | 0/0 | 4928 | 10 | 0 | 0 | 10 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0008 | 0/0 | 4939 | 10 | 0 | 0 | 10 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0009 | 0/0 | 4929 | 9 | 0 | 0 | 9 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0010 | 0/0 | 4939 | 8 | 0 | 0 | 7 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0011 | 0/0 | 4930 | 6 | 0 | 3 | 1 | 1 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0012 | 0/0 | 4934 | 6 | 5 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0013 | 0/0 | 4931 | 5 | 5 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0014 | 0/0 | 4932 | 5 | 2 | 2 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0015 | 0/0 | 4941 | 5 | 0 | 0 | 5 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0016 | 0/0 | 4934 | 4 | 0 | 2 | 0 | 2 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0017 | 0/0 | 4929 | 4 | 1 | 3 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0018 | 0/0 | 4936 | 3 | 0 | 0 | 0 | 0 | 3 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0019 | 0/0 | 4934 | 3 | 2 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0020 | 0/0 | 4936 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0021 | 0/0 | 4937 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0022 | 0/0 | 4929 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0023 | 0/0 | 4938 | 3 | 0 | 2 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0024 | 0/0 | 4931 | 3 | 0 | 0 | 0 | 0 | 3 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0025 | 0/0 | 4934 | 3 | 0 | 1 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0026 | 0/0 | 4932 | 3 | 0 | 2 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0027 | 0/0 | 4935 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0028 | 0/0 | 4934 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0029 | 0/0 | 4927 | 2 | 1 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0030 | 0/0 | 4935 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0031 | 0/0 | 4934 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0032 | 0/0 | 4930 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0033 | 0/0 | 4934 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0034 | 0/0 | 4938 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0035 | 0/0 | 4933 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0036 | 0/0 | 4933 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0037 | 0/0 | 4935 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0038 | 0/0 | 4929 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0039 | 0/0 | 4933 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0040 | 0/0 | 4940 | 2 | 0 | 0 | 1 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0041 | 0/0 | 4935 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0042 | 0/0 | 4940 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0043 | 0/0 | 4942 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0044 | 0/0 | 4931 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0045 | 0/0 | 4929 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0046 | 0/0 | 4924 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0047 | 0/0 | 4930 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0048 | 0/0 | 4933 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0049 | 0/0 | 4932 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0050 | 0/0 | 4934 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0051 | 0/0 | 4938 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0052 | 0/0 | 4929 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0053 | 0/0 | 4929 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0054 | 0/0 | 4929 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0055 | 0/0 | 4935 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0056 | 0/0 | 4929 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0057 | 0/0 | 4934 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0058 | 0/0 | 4935 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0059 | 0/0 | 4934 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0060 | 0/0 | 4932 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0061 | 0/0 | 4931 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0062 | 0/0 | 4930 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0063 | 0/0 | 4929 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0064 | 0/0 | 4939 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0065 | 0/0 | 4935 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0066 | 0/0 | 4934 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0067 | 0/0 | 4939 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0068 | 0/0 | 4933 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0069 | 0/0 | 4933 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0070 | 0/0 | 4939 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0071 | 0/0 | 4935 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0072 | 0/0 | 4937 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0073 | 0/0 | 4937 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0074 | 0/0 | 4936 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0075 | 0/0 | 4933 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0076 | 0/0 | 4933 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0077 | 0/0 | 4931 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0078 | 0/0 | 4932 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0079 | 0/0 | 4933 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0080 | 0/0 | 4936 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0081 | 0/0 | 4937 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0082 | 0/0 | 4935 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0083 | 0/0 | 4936 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0084 | 0/0 | 4937 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0085 | 0/0 | 4938 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0086 | 0/0 | 4940 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0087 | 0/0 | 4934 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0088 | 0/0 | 4935 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0089 | 0/0 | 4933 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0090 | 0/0 | 4938 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
t0091 | 0/0 | 4935 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 33 | 0 | 4 | 22 | 1 | 6 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0002 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0003 | 0/0 | 11 | 0 | 3 | 3 | 3 | 2 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0005 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0006 | 0/0 | 5 | 1 | 3 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0007 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0010 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0030 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0058 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1656 | 234 | 47 | 44 | 110 | 10 | 22 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002 | 0/1 | 1656 | 151 | 33 | 25 | 77 | 1 | 14 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0003 | 0/0 | 1656 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0004 | 0/0 | 1656 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0005 | 0/0 | 1656 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0006 | 0/0 | 1656 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 1/0 | 6584 | 50 | 6 | 11 | 29 | 1 | 2 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0003 | 0/0 | 6593 | 30 | 0 | 6 | 17 | 0 | 7 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0004 | 0/0 | 6589 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0005 | 0/0 | 6589 | 17 | 1 | 8 | 4 | 2 | 2 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0007 | 0/0 | 6583 | 10 | 0 | 0 | 10 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0008 | 0/0 | 6594 | 9 | 0 | 0 | 9 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0009 | 0/0 | 6584 | 8 | 0 | 0 | 8 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0010 | 0/0 | 6594 | 8 | 0 | 0 | 7 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0011 | 0/0 | 6585 | 6 | 0 | 3 | 1 | 1 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0013 | 0/0 | 6586 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0014 | 0/0 | 6587 | 5 | 2 | 2 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0015 | 0/0 | 6596 | 5 | 0 | 0 | 5 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0016 | 0/0 | 6589 | 4 | 0 | 2 | 0 | 2 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0017 | 0/0 | 6584 | 4 | 1 | 3 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0018 | 0/0 | 6591 | 3 | 0 | 0 | 0 | 0 | 3 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0019 | 0/0 | 6589 | 3 | 2 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0020 | 0/0 | 6591 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0021 | 0/0 | 6592 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0022 | 0/0 | 6584 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0023 | 0/0 | 6593 | 3 | 0 | 2 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0027 | 0/0 | 6590 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0028 | 0/0 | 6589 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0029 | 0/0 | 6582 | 2 | 1 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0030 | 0/0 | 6590 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0031 | 0/0 | 6589 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0032 | 0/0 | 6585 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0033 | 0/0 | 6589 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0034 | 0/0 | 6593 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0038 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0040 | 0/0 | 6595 | 2 | 0 | 0 | 1 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0042 | 0/0 | 6595 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0043 | 0/0 | 6597 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0044 | 0/0 | 6586 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0045 | 0/0 | 6584 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0046 | 0/0 | 6579 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0047 | 0/0 | 6585 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0049 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0050 | 0/0 | 6589 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0051 | 0/0 | 6593 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0052 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0053 | 0/0 | 6584 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0054 | 0/0 | 6584 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0055 | 0/0 | 6590 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0056 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0057 | 0/0 | 6589 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0058 | 0/0 | 6590 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0059 | 0/0 | 6589 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0060 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0061 | 0/0 | 6586 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0062 | 0/0 | 6585 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0063 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0064 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0065 | 0/0 | 6590 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0066 | 0/0 | 6589 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0067 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0070 | 0/0 | 6594 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0073 | 0/0 | 6592 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0074 | 0/0 | 6591 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0077 | 0/0 | 6586 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0078 | 0/0 | 6587 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0079 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0083 | 0/0 | 6591 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0085 | 0/0 | 6593 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0086 | 0/0 | 6595 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0001t0090 | 0/0 | 6593 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0001 | 0/1 | 6588 | 67 | 15 | 18 | 24 | 0 | 9 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0004 | 0/0 | 6589 | 28 | 0 | 0 | 27 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0006 | 0/0 | 6590 | 14 | 3 | 0 | 11 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0008 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0009 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0012 | 0/0 | 6589 | 6 | 5 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0024 | 0/0 | 6586 | 3 | 0 | 0 | 0 | 0 | 3 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0025 | 0/0 | 6589 | 3 | 0 | 1 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0026 | 0/0 | 6587 | 3 | 0 | 2 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0035 | 0/0 | 6588 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0036 | 0/0 | 6588 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0037 | 0/0 | 6590 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0039 | 0/0 | 6588 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0041 | 0/0 | 6590 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0048 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0068 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0069 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0071 | 0/0 | 6590 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0072 | 0/0 | 6592 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0075 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0076 | 0/0 | 6588 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0080 | 0/0 | 6591 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0081 | 0/0 | 6592 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0082 | 0/0 | 6590 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0084 | 0/0 | 6592 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0087 | 0/0 | 6589 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0088 | 0/0 | 6590 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0089 | 0/0 | 6588 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0002t0091 | 0/0 | 6590 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0003t0002 | 0/0 | 6584 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0003t0038 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0004t0013 | 0/0 | 6586 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0005t0001 | 0/0 | 6588 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
a0001c0006t0003 | 0/0 | 6593 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | copy fasta | chr12 | 69234569 | 69279358 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0006 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0008 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0058 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0003g0001 | 0/0 | 14 | 0 | 4 | 5 | 0 | 5 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0005g0003 | 0/0 | 6 | 0 | 2 | 3 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0005g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0005g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0007g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0007g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0007g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0007g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0007g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0007g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0007g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0007g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0008g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0008g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0008g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0008g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0009g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0009g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0009g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0009g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0009g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0009g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0010g0001 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0010g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0010g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0011g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0011g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0011g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0011g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0011g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0011g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0013g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0013g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0013g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0014g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0014g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0014g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0014g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0015g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0015g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0015g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0015g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0016g0003 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0016g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0017g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0017g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0017g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0017g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0018g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0018g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0019g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0019g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0020g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0020g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0020g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0021g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0021g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0021g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0022g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0022g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0022g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0023g0010 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0027g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0028g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0029g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0029g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0030g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0030g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0031g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0031g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0032g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0032g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0033g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0033g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0034g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0034g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0038g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0040g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0040g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0042g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0042g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0043g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0044g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0045g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0046g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0047g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0049g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0050g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0051g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0052g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0053g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0054g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0055g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0056g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0057g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0058g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0059g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0060g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0061g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0062g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0063g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0064g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0065g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0066g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0067g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0070g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0073g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0074g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0077g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0078g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0079g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0083g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0085g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0086g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0001t0090g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0004g0002 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0004g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0006g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0006g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0006g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0006g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0006g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0006g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0008g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0009g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0012g0005 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0012g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0024g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0024g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0024g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0025g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0025g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0025g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0026g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0026g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0026g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0035g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0035g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0036g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0037g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0037g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0039g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0039g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0041g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0041g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0048g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0068g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0069g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0071g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0072g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0075g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0076g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0080g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0081g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0082g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0084g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0087g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0088g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0089g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0002t0091g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0003t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0003t0038g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0004t0013g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0004t0013g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0005t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
a0001c0006t0003g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0005 | g0018 | EUR | FIN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00280 | hp2 | a0001 | c0006 | t0003 | g0001 | EUR | FIN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00323 | hp1 | a0001 | c0001 | t0005 | g0003 | EUR | FIN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00323 | hp2 | a0001 | c0001 | t0011 | g0252 | EUR | FIN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00438 | hp1 | a0001 | c0002 | t0004 | g0101 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00438 | hp2 | a0001 | c0001 | t0009 | g0007 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00544 | hp1 | a0001 | c0001 | t0005 | g0235 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00544 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00558 | hp2 | a0001 | c0003 | t0002 | g0015 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00597 | hp1 | a0001 | c0001 | t0007 | g0038 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00597 | hp2 | a0001 | c0002 | t0004 | g0004 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00621 | hp2 | a0001 | c0002 | t0004 | g0004 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00639 | hp1 | a0001 | c0001 | t0078 | g0013 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00639 | hp2 | a0001 | c0001 | t0011 | g0214 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00642 | hp1 | a0001 | c0001 | t0028 | g0043 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00673 | hp1 | a0001 | c0002 | t0006 | g0163 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00673 | hp2 | a0001 | c0001 | t0038 | g0243 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00733 | hp2 | a0001 | c0001 | t0023 | g0010 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00738 | hp1 | a0001 | c0002 | t0026 | g0119 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00738 | hp2 | a0001 | c0001 | t0029 | g0227 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0238 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG00741 | hp2 | a0001 | c0001 | t0011 | g0198 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01069 | hp1 | a0001 | c0002 | t0035 | g0138 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01070 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01070 | hp2 | a0001 | c0001 | t0023 | g0010 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01071 | hp2 | a0001 | c0002 | t0035 | g0145 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01074 | hp2 | a0001 | c0001 | t0005 | g0018 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0139 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0154 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01106 | hp2 | a0001 | c0001 | t0028 | g0043 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01167 | hp1 | a0001 | c0001 | t0017 | g0007 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01167 | hp2 | a0001 | c0001 | t0019 | g0019 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01168 | hp1 | a0001 | c0002 | t0026 | g0225 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01168 | hp2 | a0001 | c0001 | t0005 | g0239 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01169 | hp1 | a0001 | c0001 | t0005 | g0017 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01169 | hp2 | a0001 | c0001 | t0017 | g0213 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01175 | hp2 | a0001 | c0001 | t0014 | g0021 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01192 | hp2 | a0001 | c0001 | t0059 | g0059 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01256 | hp2 | a0001 | c0001 | t0016 | g0017 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0123 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01257 | hp2 | a0001 | c0001 | t0017 | g0041 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0129 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01258 | hp2 | a0001 | c0001 | t0016 | g0003 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01261 | hp1 | a0001 | c0001 | t0011 | g0192 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01346 | hp1 | a0001 | c0002 | t0076 | g0152 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0108 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0118 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01361 | hp2 | a0001 | c0002 | t0012 | g0005 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0236 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01433 | hp2 | a0001 | c0002 | t0025 | g0107 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0153 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0127 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01516 | hp1 | a0001 | c0001 | t0014 | g0061 | EUR | IBS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01516 | hp2 | a0001 | c0001 | t0016 | g0003 | EUR | IBS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01517 | hp1 | a0001 | c0002 | t0026 | g0051 | EUR | IBS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01517 | hp2 | a0001 | c0001 | t0016 | g0003 | EUR | IBS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01884 | hp1 | a0001 | c0002 | t0012 | g0005 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01884 | hp2 | a0001 | c0001 | t0049 | g0263 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01891 | hp1 | a0001 | c0002 | t0006 | g0113 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0233 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01928 | hp2 | a0001 | c0005 | t0001 | g0135 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0146 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0071 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01978 | hp2 | a0001 | c0001 | t0070 | g0010 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0132 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0255 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02015 | hp2 | a0001 | c0002 | t0004 | g0028 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02027 | hp1 | a0001 | c0001 | t0007 | g0171 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02027 | hp2 | a0001 | c0002 | t0041 | g0111 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02040 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02040 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02055 | hp1 | a0001 | c0001 | t0013 | g0042 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02055 | hp2 | a0001 | c0002 | t0069 | g0122 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02056 | hp2 | a0001 | c0001 | t0009 | g0202 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02080 | hp1 | a0001 | c0001 | t0067 | g0001 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02080 | hp2 | a0001 | c0001 | t0056 | g0008 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02083 | hp1 | a0001 | c0001 | t0052 | g0209 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02129 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02129 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02132 | hp1 | a0001 | c0002 | t0004 | g0102 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02135 | hp1 | a0001 | c0001 | t0011 | g0037 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02135 | hp2 | a0001 | c0002 | t0004 | g0142 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02145 | hp1 | a0001 | c0001 | t0043 | g0022 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0046 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CDX | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | CDX | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | CDX | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | CDX | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02258 | hp1 | a0001 | c0001 | t0017 | g0006 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02300 | hp1 | a0001 | c0001 | t0014 | g0021 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0093 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02451 | hp2 | a0001 | c0002 | t0036 | g0012 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02523 | hp1 | a0001 | c0001 | t0007 | g0172 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02572 | hp1 | a0001 | c0002 | t0068 | g0085 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02572 | hp2 | a0001 | c0001 | t0033 | g0185 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02602 | hp1 | a0001 | c0001 | t0046 | g0017 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02602 | hp2 | a0001 | c0001 | t0053 | g0199 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02615 | hp1 | a0001 | c0001 | t0079 | g0013 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0244 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0089 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02683 | hp1 | a0001 | c0001 | t0086 | g0068 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0117 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02698 | hp1 | a0001 | c0001 | t0011 | g0241 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02698 | hp2 | a0001 | c0001 | t0005 | g0237 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02717 | hp1 | a0001 | c0002 | t0091 | g0125 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02717 | hp2 | a0001 | c0001 | t0055 | g0264 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02723 | hp2 | a0001 | c0001 | t0030 | g0176 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02735 | hp1 | a0001 | c0001 | t0018 | g0003 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02818 | hp1 | a0001 | c0002 | t0012 | g0005 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02818 | hp2 | a0001 | c0001 | t0021 | g0230 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02886 | hp1 | a0001 | c0002 | t0081 | g0100 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02895 | hp2 | a0001 | c0002 | t0072 | g0005 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02896 | hp1 | a0001 | c0002 | t0012 | g0005 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02896 | hp2 | a0001 | c0001 | t0065 | g0203 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02897 | hp1 | a0001 | c0002 | t0012 | g0083 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02922 | hp1 | a0001 | c0001 | t0033 | g0186 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02965 | hp1 | a0001 | c0001 | t0029 | g0228 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02976 | hp1 | a0001 | c0001 | t0014 | g0262 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02976 | hp2 | a0001 | c0001 | t0058 | g0064 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03098 | hp1 | a0001 | c0001 | t0020 | g0179 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03098 | hp2 | a0001 | c0001 | t0060 | g0182 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03139 | hp1 | a0001 | c0001 | t0014 | g0265 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03139 | hp2 | a0001 | c0002 | t0036 | g0012 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03195 | hp1 | a0001 | c0001 | t0020 | g0177 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03195 | hp2 | a0001 | c0002 | t0037 | g0086 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03209 | hp1 | a0001 | c0002 | t0012 | g0005 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03209 | hp2 | a0001 | c0001 | t0032 | g0184 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03225 | hp1 | a0001 | c0001 | t0032 | g0183 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03225 | hp2 | a0001 | c0001 | t0027 | g0045 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03239 | hp2 | a0001 | c0002 | t0024 | g0031 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03453 | hp1 | a0001 | c0001 | t0050 | g0019 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03453 | hp2 | a0001 | c0001 | t0031 | g0219 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03486 | hp1 | a0001 | c0001 | t0030 | g0178 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03486 | hp2 | a0001 | c0002 | t0037 | g0087 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0112 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0115 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03516 | hp1 | a0001 | c0002 | t0006 | g0030 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03516 | hp2 | a0001 | c0001 | t0021 | g0053 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03688 | hp1 | a0001 | c0001 | t0054 | g0056 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03688 | hp2 | a0001 | c0002 | t0024 | g0143 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03704 | hp1 | a0001 | c0002 | t0004 | g0128 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03704 | hp2 | a0001 | c0001 | t0018 | g0003 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0156 | SAS | BEB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03831 | hp2 | a0001 | c0001 | t0010 | g0001 | SAS | BEB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0114 | SAS | BEB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0149 | SAS | BEB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0074 | SAS | BEB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03942 | hp1 | a0001 | c0002 | t0024 | g0130 | SAS | BEB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03942 | hp2 | a0001 | c0001 | t0005 | g0232 | SAS | BEB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0106 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG04115 | hp2 | a0001 | c0001 | t0040 | g0082 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG04199 | hp1 | a0001 | c0001 | t0018 | g0240 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG04204 | hp1 | a0001 | c0001 | t0085 | g0080 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0137 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0194 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0090 | AFR | YRI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18522 | hp2 | a0001 | c0002 | t0006 | g0116 | AFR | YRI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | CHB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | CHB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18747 | hp1 | a0001 | c0001 | t0022 | g0207 | EAS | CHB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | CHB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18906 | hp1 | a0001 | c0001 | t0043 | g0022 | AFR | YRI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18906 | hp2 | a0001 | c0002 | t0071 | g0012 | AFR | YRI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18942 | hp2 | a0001 | c0002 | t0004 | g0224 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18944 | hp1 | a0001 | c0001 | t0007 | g0173 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18944 | hp2 | a0001 | c0002 | t0082 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18945 | hp2 | a0001 | c0002 | t0006 | g0157 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18946 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18946 | hp2 | a0001 | c0002 | t0039 | g0014 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18947 | hp2 | a0001 | c0002 | t0088 | g0168 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18948 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18949 | hp1 | a0001 | c0001 | t0047 | g0234 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18949 | hp2 | a0001 | c0001 | t0015 | g0076 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18950 | hp1 | a0001 | c0001 | t0008 | g0075 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18950 | hp2 | a0001 | c0002 | t0087 | g0096 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18952 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18953 | hp2 | a0001 | c0002 | t0041 | g0004 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18954 | hp1 | a0001 | c0001 | t0008 | g0072 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18956 | hp1 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18956 | hp2 | a0001 | c0001 | t0034 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18957 | hp1 | a0001 | c0002 | t0025 | g0150 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18957 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18959 | hp1 | a0001 | c0002 | t0006 | g0160 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18960 | hp1 | a0001 | c0001 | t0040 | g0077 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18961 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18961 | hp2 | a0001 | c0001 | t0007 | g0212 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18962 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18963 | hp2 | a0001 | c0001 | t0022 | g0204 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18964 | hp2 | a0001 | c0002 | t0006 | g0164 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18965 | hp1 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18966 | hp1 | a0001 | c0002 | t0006 | g0220 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18967 | hp1 | a0001 | c0002 | t0080 | g0162 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18968 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18970 | hp1 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18970 | hp2 | a0001 | c0002 | t0006 | g0166 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18971 | hp1 | a0001 | c0002 | t0004 | g0035 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18971 | hp2 | a0001 | c0001 | t0062 | g0260 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18972 | hp1 | a0001 | c0002 | t0048 | g0034 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18972 | hp2 | a0001 | c0001 | t0007 | g0016 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18974 | hp2 | a0001 | c0001 | t0090 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18975 | hp1 | a0001 | c0003 | t0002 | g0015 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18975 | hp2 | a0001 | c0001 | t0008 | g0024 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18977 | hp2 | a0001 | c0002 | t0006 | g0158 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18979 | hp2 | a0001 | c0001 | t0074 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18980 | hp1 | a0001 | c0001 | t0009 | g0218 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18980 | hp2 | a0001 | c0001 | t0042 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18982 | hp1 | a0001 | c0002 | t0004 | g0109 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18982 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18983 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18984 | hp1 | a0001 | c0002 | t0006 | g0167 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18984 | hp2 | a0001 | c0001 | t0015 | g0026 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18986 | hp2 | a0001 | c0001 | t0083 | g0025 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18988 | hp1 | a0001 | c0001 | t0010 | g0023 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18988 | hp2 | a0001 | c0002 | t0039 | g0029 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18989 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18991 | hp1 | a0001 | c0001 | t0034 | g0094 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18994 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18994 | hp2 | a0001 | c0001 | t0022 | g0217 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18995 | hp2 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18998 | hp1 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18998 | hp2 | a0001 | c0001 | t0015 | g0070 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18999 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18999 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19006 | hp1 | a0001 | c0001 | t0010 | g0023 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19006 | hp2 | a0001 | c0002 | t0006 | g0165 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19009 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19010 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19011 | hp2 | a0001 | c0001 | t0007 | g0040 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19012 | hp1 | a0001 | c0002 | t0025 | g0030 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19043 | hp1 | a0001 | c0001 | t0013 | g0231 | AFR | LWK | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19043 | hp2 | a0001 | c0001 | t0057 | g0226 | AFR | LWK | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19054 | hp2 | a0001 | c0002 | t0008 | g0084 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19058 | hp1 | a0001 | c0003 | t0038 | g0015 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19058 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19060 | hp1 | a0001 | c0002 | t0006 | g0161 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19060 | hp2 | a0001 | c0001 | t0009 | g0201 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19064 | hp1 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19066 | hp1 | a0001 | c0001 | t0009 | g0259 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19068 | hp1 | a0001 | c0001 | t0061 | g0011 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19068 | hp2 | a0001 | c0002 | t0004 | g0035 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19070 | hp1 | a0001 | c0001 | t0007 | g0211 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19076 | hp1 | a0001 | c0002 | t0009 | g0097 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19076 | hp2 | a0001 | c0002 | t0004 | g0098 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19077 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19078 | hp1 | a0001 | c0001 | t0042 | g0079 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19078 | hp2 | a0001 | c0001 | t0044 | g0257 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19080 | hp1 | a0001 | c0001 | t0010 | g0065 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19080 | hp2 | a0001 | c0002 | t0004 | g0155 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19082 | hp1 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19082 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19083 | hp2 | a0001 | c0002 | t0084 | g0221 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19085 | hp1 | a0001 | c0001 | t0007 | g0039 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19085 | hp2 | a0001 | c0002 | t0006 | g0159 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19087 | hp2 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19090 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19091 | hp2 | a0001 | c0002 | t0075 | g0120 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19240 | hp1 | a0001 | c0001 | t0031 | g0256 | AFR | YRI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA19240 | hp2 | a0001 | c0001 | t0019 | g0019 | AFR | YRI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | ASW | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA20129 | hp2 | a0001 | c0001 | t0021 | g0042 | AFR | ASW | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA20752 | hp1 | a0001 | c0001 | t0023 | g0010 | EUR | TSI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0193 | EUR | TSI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA20805 | hp1 | a0001 | c0001 | t0045 | g0188 | EUR | TSI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA20805 | hp2 | a0001 | c0001 | t0051 | g0175 | EUR | TSI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0049 | SAS | GIH | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA20905 | hp2 | a0001 | c0002 | t0089 | g0031 | SAS | GIH | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01123 | hp1 | a0001 | c0001 | t0005 | g0018 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02109 | hp2 | a0001 | c0001 | t0066 | g0181 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02486 | hp1 | a0001 | c0001 | t0064 | g0242 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02486 | hp2 | a0001 | c0004 | t0013 | g0245 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02559 | hp1 | a0001 | c0001 | t0019 | g0261 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG02559 | hp2 | a0001 | c0001 | t0077 | g0013 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG03471 | hp2 | a0001 | c0004 | t0013 | g0222 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG06807 | hp1 | a0001 | c0001 | t0020 | g0229 | AFR | USA | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
HG06807 | hp2 | a0001 | c0001 | t0013 | g0052 | AFR | USA | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18955 | hp1 | a0001 | c0001 | t0007 | g0039 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA18955 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0141 | AFR | USA | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA20300 | hp2 | a0001 | c0001 | t0063 | g0057 | AFR | USA | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA21309 | hp1 | a0001 | c0001 | t0073 | g0180 | AFR | LWK | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
NA21309 | hp2 | a0001 | c0001 | t0027 | g0045 | AFR | LWK | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0147 | REF | REF | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0058 | REF | REF | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:69251284
|
T | G | 1 | a0001c0004 | 2 | HG02486.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.216T>G | p.Val72Val | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/10 | 294/6584 | 216/1656 | 72/551 | chr12 | 69251284 | ||
chr12:69253134
|
G | A | 2 | a0001c0002a0001c0005 | 152 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
synonymous_variant | LOW | c.354G>A | p.Arg118Arg | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/10 | 432/6584 | 354/1656 | 118/551 | chr12 | 69253134 | ||
chr12:69258948
|
A | G | 1 | a0001c0006 | 1 | HG00280.hp2 | synonymous_variant | LOW | c.1053A>G | p.Pro351Pro | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 6/10 | 1131/6584 | 1053/1656 | 351/551 | chr12 | 69258948 | ||
chr12:69258960
|
G | A | 1 | a0001c0003 | 3 | HG00558.hp2 NA18975.hp1 NA19058.hp1 |
synonymous_variant | LOW | c.1065G>A | p.Pro355Pro | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 6/10 | 1143/6584 | 1065/1656 | 355/551 | chr12 | 69258960 | ||
chr12:69260183
|
T | C | 1 | a0001c0005 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.1455T>C | p.Tyr485Tyr | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/10 | 1533/6584 | 1455/1656 | 485/551 | chr12 | 69260183 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:69239571
|
T | C | 1 | a0001c0001t0044 | 1 | NA19078.hp2 | 5_prime_UTR_variant | MODIFIER | c.-76T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/10 | 76 | chr12 | 69239571 | |||||
chr12:69239599
|
A | G | 52 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(49): Show | 228 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(225): Show |
5_prime_UTR_variant | MODIFIER | c.-48A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/10 | 48 | chr12 | 69239599 | |||||
chr12:69239636
|
G | A | 1 | a0001c0001t0045 | 1 | NA20805.hp1 | 5_prime_UTR_variant | MODIFIER | c.-11G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/10 | 11 | chr12 | 69239636 | |||||
chr12:69269567
|
C | T | 1 | a0001c0001t0043 | 2 | HG02145.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*59C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7008 | chr12 | 69269567 | |||||
chr12:69269759
|
A | G | 1 | a0001c0002t0091 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*251A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7200 | chr12 | 69269759 | |||||
chr12:69269782
|
T | C | 1 | a0001c0001t0027 | 2 | HG03225.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*274T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7223 | chr12 | 69269782 | |||||
chr12:69269805
|
A | G | 1 | a0001c0001t0027 | 2 | HG03225.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*297A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7246 | chr12 | 69269805 | |||||
chr12:69269905
|
A | G | 1 | a0001c0001t0066 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*397A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7346 | chr12 | 69269905 | |||||
chr12:69270065
|
G | A | 2 | a0001c0001t0034a0001c0001t0067 | 3 | HG02080.hp1 NA18956.hp2 NA18991.hp1 |
3_prime_UTR_variant | MODIFIER | c.*557G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7506 | chr12 | 69270065 | |||||
chr12:69270072
|
G | C | 6 | a0001c0001t0005a0001c0001t0016a0001c0001t0018others(3): Show | 28 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*564G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7513 | chr12 | 69270072 | |||||
chr12:69270073
|
A | G | 1 | a0001c0001t0028 | 2 | HG00642.hp1 HG01106.hp2 |
3_prime_UTR_variant | MODIFIER | c.*565A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7514 | chr12 | 69270073 | |||||
chr12:69270205
|
T | A | 1 | a0001c0002t0048 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*697T>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7646 | chr12 | 69270205 | |||||
chr12:69270356
|
T | C | 1 | a0001c0002t0068 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*848T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7797 | chr12 | 69270356 | |||||
chr12:69270620
|
A | G | 2 | a0001c0001t0065a0001c0001t0066 | 2 | HG02109.hp2 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1112A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8061 | chr12 | 69270620 | |||||
chr12:69270714
|
A | T | 1 | a0001c0001t0090 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1206A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8155 | chr12 | 69270714 | |||||
chr12:69270799
|
G | A | 1 | a0001c0002t0035 | 2 | HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1291G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8240 | chr12 | 69270799 | |||||
chr12:69270822
|
G | T | 1 | a0001c0001t0064 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1314G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8263 | chr12 | 69270822 | |||||
chr12:69270856
|
C | G | 1 | a0001c0001t0033 | 2 | HG02572.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1348C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8297 | chr12 | 69270856 | |||||
chr12:69270862
|
T | C | 3 | a0001c0001t0019a0001c0001t0049a0001c0001t0050 | 5 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1354T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8303 | chr12 | 69270862 | |||||
chr12:69271046
|
T | C | 1 | a0001c0002t0069 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1538T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8487 | chr12 | 69271046 | |||||
chr12:69271271
|
A | G | 1 | a0001c0001t0063 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1763A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8712 | chr12 | 69271271 | |||||
chr12:69271278
|
C | A | 1 | a0001c0001t0064 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1770C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8719 | chr12 | 69271278 | |||||
chr12:69271455
|
G | T | 1 | a0001c0002t0089 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1947G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8896 | chr12 | 69271455 | |||||
chr12:69271529
|
T | C | 3 | a0001c0001t0023a0001c0001t0051a0001c0001t0070 | 5 | HG00733.hp2 HG01070.hp2 HG01978.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2021T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8970 | chr12 | 69271529 | |||||
chr12:69271742
|
A | G | 5 | a0001c0001t0009a0001c0001t0044a0001c0001t0061others(2): Show | 12 | HG00438.hp2 HG02056.hp2 NA18971.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2234A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9183 | chr12 | 69271742 | |||||
chr12:69271830
|
T | G | 1 | a0001c0001t0064 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2322T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9271 | chr12 | 69271830 | |||||
chr12:69271855
|
C | T | 1 | a0001c0002t0088 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2347C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9296 | chr12 | 69271855 | |||||
chr12:69272012
|
G | T | 1 | a0001c0002t0087 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2504G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9453 | chr12 | 69272012 | |||||
chr12:69272152
|
T | C | 1 | a0001c0001t0052 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2644T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9593 | chr12 | 69272152 | |||||
chr12:69272155
|
G | GT | 33 | a0001c0001t0005a0001c0001t0016a0001c0001t0018others(30): Show | 143 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*2659dupT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9609 | INFO_REALIGN_3_PRIME | chr12 | 69272155 | ||||
chr12:69272155
|
G | GTT | 18 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(15): Show | 90 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2658_*2659dupTT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9609 | INFO_REALIGN_3_PRIME | chr12 | 69272155 | ||||
chr12:69272155
|
G | GTTT | 4 | a0001c0001t0008a0001c0001t0042a0001c0002t0008others(1): Show | 14 | HG02027.hp2 HG02040.hp1 NA18946.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2657_*2659dupTTT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9609 | INFO_REALIGN_3_PRIME | chr12 | 69272155 | ||||
chr12:69272156
|
T | G | 1 | a0001c0001t0053 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2648T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9597 | chr12 | 69272156 | |||||
chr12:69272178
|
A | G | 1 | a0001c0001t0086 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2670A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9619 | chr12 | 69272178 | |||||
chr12:69272268
|
A | C | 1 | a0001c0001t0086 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2760A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9709 | chr12 | 69272268 | |||||
chr12:69272295
|
A | T | 1 | a0001c0001t0060 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2787A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9736 | chr12 | 69272295 | |||||
chr12:69272499
|
A | G | 1 | a0001c0001t0050 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2991A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9940 | chr12 | 69272499 | |||||
chr12:69272782
|
G | A | 1 | a0001c0001t0054 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3274G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10223 | chr12 | 69272782 | |||||
chr12:69272847
|
C | T | 3 | a0001c0001t0023a0001c0001t0051a0001c0001t0070 | 5 | HG00733.hp2 HG01070.hp2 HG01978.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3339C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10288 | chr12 | 69272847 | |||||
chr12:69272859
|
C | G | 1 | a0001c0001t0022 | 3 | NA18747.hp1 NA18963.hp2 NA18994.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3351C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10300 | chr12 | 69272859 | |||||
chr12:69272869
|
A | AGT | 23 | a0001c0001t0013a0001c0001t0014a0001c0001t0020others(20): Show | 49 | HG00639.hp1 HG00673.hp1 HG01175.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3388_*3389dupGT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10339 | INFO_REALIGN_3_PRIME | chr12 | 69272869 | ||||
chr12:69272869
|
A | AGTGT | 16 | a0001c0001t0003a0001c0001t0008a0001c0001t0010others(13): Show | 64 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*3386_*3389dupGTGT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10339 | INFO_REALIGN_3_PRIME | chr12 | 69272869 | ||||
chr12:69272869
|
A | AGTGTGT | 7 | a0001c0001t0015a0001c0001t0031a0001c0001t0033others(4): Show | 14 | HG02109.hp2 HG02572.hp2 HG02683.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3384_*3389dupGTGT others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10339 | INFO_REALIGN_3_PRIME | chr12 | 69272869 | ||||
chr12:69272869
|
A | AGTGTGTG others(1): Show |
4 | a0001c0001t0023a0001c0001t0043a0001c0001t0051others(1): Show | 7 | HG00733.hp2 HG01070.hp2 HG01978.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3382_*3389dupGTGT others(4): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10339 | INFO_REALIGN_3_PRIME | chr12 | 69272869 | ||||
chr12:69272869
|
AGT | A | 7 | a0001c0001t0005a0001c0001t0016a0001c0001t0028others(4): Show | 32 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3388_*3389delGT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10337 | INFO_REALIGN_3_PRIME | chr12 | 69272869 | ||||
chr12:69272869
|
AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0046 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3378_*3389delGTGT others(8): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10327 | INFO_REALIGN_3_PRIME | chr12 | 69272869 | ||||
chr12:69272956
|
A | G | 1 | a0001c0001t0056 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3448A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10397 | chr12 | 69272956 | |||||
chr12:69273260
|
G | A | 1 | a0001c0001t0016 | 4 | HG01256.hp2 HG01258.hp2 HG01516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3752G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10701 | chr12 | 69273260 | |||||
chr12:69273295
|
T | A | 51 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(48): Show | 227 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*3787T>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10736 | chr12 | 69273295 | |||||
chr12:69273343
|
A | G | 2 | a0001c0001t0017a0001c0001t0045 | 5 | HG01167.hp1 HG01169.hp2 HG01257.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3835A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10784 | chr12 | 69273343 | |||||
chr12:69273680
|
A | C | 1 | a0001c0002t0076 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4172A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11121 | chr12 | 69273680 | |||||
chr12:69273883
|
C | G | 1 | a0001c0001t0058 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4375C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11324 | chr12 | 69273883 | |||||
chr12:69274003
|
A | C | 1 | a0001c0001t0085 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4495A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11444 | chr12 | 69274003 | |||||
chr12:69274109
|
C | CT | 9 | a0001c0001t0011a0001c0001t0014a0001c0001t0019others(6): Show | 20 | HG00323.hp2 HG00639.hp2 HG00741.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4619dupT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11569 | INFO_REALIGN_3_PRIME | chr12 | 69274109 | ||||
chr12:69274109
|
C | CTTT | 33 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(30): Show | 186 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*4617_*4619dupTTT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11569 | INFO_REALIGN_3_PRIME | chr12 | 69274109 | ||||
chr12:69274109
|
C | CTTTT | 14 | a0001c0001t0010a0001c0001t0015a0001c0001t0027others(11): Show | 31 | HG00544.hp2 HG01433.hp2 HG02080.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*4616_*4619dupTTTT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11569 | INFO_REALIGN_3_PRIME | chr12 | 69274109 | ||||
chr12:69274109
|
C | CTTTTT | 2 | a0001c0001t0020a0001c0002t0012 | 9 | HG01361.hp2 HG01884.hp1 HG02818.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4615_*4619dupTTTT others(1): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11569 | INFO_REALIGN_3_PRIME | chr12 | 69274109 | ||||
chr12:69274109
|
C | CTTTTTT | 11 | a0001c0001t0005a0001c0001t0016a0001c0001t0018others(8): Show | 36 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*4614_*4619dupTTTT others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11569 | INFO_REALIGN_3_PRIME | chr12 | 69274109 | ||||
chr12:69274109
|
CT | C | 5 | a0001c0001t0007a0001c0001t0031a0001c0001t0033others(2): Show | 16 | HG00597.hp1 HG02027.hp1 HG02109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4619delT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11568 | INFO_REALIGN_3_PRIME | chr12 | 69274109 | ||||
chr12:69274178
|
C | T | 1 | a0001c0002t0075 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4670C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11619 | chr12 | 69274178 | |||||
chr12:69274225
|
C | T | 1 | a0001c0002t0039 | 2 | NA18946.hp2 NA18988.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4717C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11666 | chr12 | 69274225 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:69239765
|
A | C | 8 | a0001c0001t0014g0262a0001c0001t0014g0265a0001c0001t0019g0019others(5): Show | 10 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.60+59A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69239765 | ||||||
chr12:69239892
|
G | T | 4 | a0001c0001t0002g0258a0001c0001t0009g0259a0001c0001t0044g0257others(1): Show | 4 | NA18971.hp2 NA19066.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.60+186G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69239892 | ||||||
chr12:69239941
|
G | C | 1 | a0001c0002t0001g0046 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.60+235G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69239941 | ||||||
chr12:69239979
|
G | C | 1 | a0001c0001t0003g0047 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.60+273G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69239979 | ||||||
chr12:69240061
|
G | A | 1 | a0001c0001t0002g0048 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.60+355G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240061 | ||||||
chr12:69240084
|
C | T | 1 | a0001c0001t0031g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.60+378C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240084 | ||||||
chr12:69240105
|
G | A | 1 | a0001c0002t0001g0049 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.60+399G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240105 | ||||||
chr12:69240136
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.60+430G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240136 | ||||||
chr12:69240147
|
C | T | 1 | a0001c0002t0001g0255 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.60+441C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240147 | ||||||
chr12:69240168
|
C | G | 2 | a0001c0002t0001g0253a0001c0002t0001g0254 | 2 | HG00609.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.60+462C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240168 | ||||||
chr12:69240203
|
C | T | 1 | a0001c0001t0011g0252 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.60+497C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240203 | ||||||
chr12:69240206
|
T | G | 1 | a0001c0002t0026g0051 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.60+500T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240206 | ||||||
chr12:69240221
|
G | A | 1 | a0001c0001t0003g0020 | 2 | NA18963.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.60+515G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240221 | ||||||
chr12:69240229
|
G | C | 2 | a0001c0001t0013g0052a0001c0001t0021g0053 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.60+523G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240229 | ||||||
chr12:69240251
|
T | G | 1 | a0001c0002t0001g0054 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.60+545T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240251 | ||||||
chr12:69240363
|
C | T | 11 | a0001c0001t0002g0008a0001c0001t0002g0044a0001c0001t0002g0048others(8): Show | 15 | HG01099.hp2 HG01981.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.60+657C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240363 | ||||||
chr12:69240374
|
A | G | 1 | a0001c0004t0013g0245 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.60+668A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240374 | ||||||
chr12:69240580
|
A | G | 1 | a0001c0002t0001g0244 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.60+874A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240580 | ||||||
chr12:69240858
|
G | A | 1 | a0001c0001t0013g0052 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.60+1152G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240858 | ||||||
chr12:69240904
|
T | C | 1 | a0001c0002t0001g0055 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.60+1198T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240904 | ||||||
chr12:69240926
|
G | A | 1 | a0001c0001t0054g0056 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.60+1220G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240926 | ||||||
chr12:69241099
|
G | T | 1 | a0001c0001t0038g0243 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.60+1393G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69241099 | ||||||
chr12:69241105
|
C | T | 1 | a0001c0001t0014g0265 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.60+1399C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69241105 | ||||||
chr12:69241530
|
G | A | 7 | a0001c0001t0014g0262a0001c0001t0014g0265a0001c0001t0019g0019others(4): Show | 8 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.60+1824G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69241530 | ||||||
chr12:69241696
|
A | G | 306 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(303): Show | 391 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(388): Show |
intron_variant | MODIFIER | c.60+1990A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69241696 | ||||||
chr12:69241925
|
C | CA | 12 | a0001c0001t0002g0060a0001c0001t0014g0021a0001c0001t0014g0061others(9): Show | 14 | HG01167.hp2 HG01175.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.60+2233dupA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69241925 | |||||
chr12:69241925
|
CA | C | 37 | a0001c0001t0002g0251a0001c0001t0003g0223a0001c0001t0005g0003others(34): Show | 48 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.60+2233delA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69241925 | |||||
chr12:69241956
|
T | C | 1 | a0001c0004t0013g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.60+2250T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69241956 | ||||||
chr12:69241957
|
T | C | 2 | a0001c0001t0013g0042a0001c0001t0021g0042 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.60+2251T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69241957 | ||||||
chr12:69242085
|
C | A | 2 | a0001c0002t0036g0012a0001c0002t0071g0012 | 3 | HG02451.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.60+2379C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242085 | ||||||
chr12:69242093
|
T | C | 1 | a0001c0002t0001g0062 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.60+2387T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242093 | ||||||
chr12:69242203
|
T | TA | 169 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(166): Show | 223 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.60+2507dupA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69242203 | |||||
chr12:69242213
|
A | C | 1 | a0001c0001t0064g0242 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.60+2507A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242213 | ||||||
chr12:69242246
|
T | C | 1 | a0001c0001t0003g0063 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.60+2540T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242246 | ||||||
chr12:69242302
|
T | C | 1 | a0001c0001t0002g0170 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.60+2596T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242302 | ||||||
chr12:69242305
|
G | A | 3 | a0001c0001t0007g0171a0001c0001t0007g0172a0001c0001t0007g0173 | 3 | HG02027.hp1 HG02523.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.60+2599G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242305 | ||||||
chr12:69242340
|
A | G | 1 | a0001c0001t0003g0169 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.60+2634A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242340 | ||||||
chr12:69242343
|
CT | C | 7 | a0001c0001t0002g0174a0001c0001t0014g0262a0001c0001t0014g0265others(4): Show | 8 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.60+2641delT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69242343 | |||||
chr12:69242444
|
G | A | 3 | a0001c0001t0023g0010a0001c0001t0051g0175a0001c0001t0070g0010 | 5 | HG00733.hp2 HG01070.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.60+2738G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242444 | ||||||
chr12:69242534
|
G | T | 105 | a0001c0002t0001g0014a0001c0002t0001g0028a0001c0002t0001g0029others(102): Show | 124 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.60+2828G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242534 | ||||||
chr12:69242542
|
G | T | 1 | a0001c0001t0034g0094 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.60+2836G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242542 | ||||||
chr12:69242831
|
G | A | 1 | a0001c0002t0001g0062 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.60+3125G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242831 | ||||||
chr12:69242901
|
G | T | 1 | a0001c0001t0031g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.60+3195G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242901 | ||||||
chr12:69242916
|
C | T | 7 | a0001c0001t0014g0262a0001c0001t0014g0265a0001c0001t0019g0019others(4): Show | 8 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.60+3210C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242916 | ||||||
chr12:69243092
|
C | CA | 7 | a0001c0001t0020g0177a0001c0001t0020g0179a0001c0001t0030g0176others(4): Show | 7 | HG02723.hp2 HG02976.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.60+3396dupA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69243092 | |||||
chr12:69243224
|
C | A | 1 | a0001c0001t0066g0181 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.60+3518C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69243224 | ||||||
chr12:69243237
|
G | A | 2 | a0001c0001t0029g0227a0001c0001t0029g0228 | 2 | HG00738.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.60+3531G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69243237 | ||||||
chr12:69243259
|
T | A | 1 | a0001c0002t0001g0095 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.60+3553T>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69243259 | ||||||
chr12:69243381
|
C | T | 10 | a0001c0002t0001g0009a0001c0002t0001g0027a0001c0002t0001g0062others(7): Show | 14 | HG01069.hp2 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.60+3675C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69243381 | ||||||
chr12:69243680
|
A | G | 1 | a0001c0002t0001g0049 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.60+3974A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69243680 | ||||||
chr12:69243888
|
C | T | 1 | a0001c0001t0009g0218 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.60+4182C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69243888 | ||||||
chr12:69243889
|
G | A | 1 | a0001c0001t0010g0065 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.60+4183G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69243889 | ||||||
chr12:69244007
|
A | T | 14 | a0001c0002t0006g0157a0001c0002t0006g0158a0001c0002t0006g0159others(11): Show | 14 | HG00673.hp1 NA18945.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.60+4301A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244007 | ||||||
chr12:69244057
|
A | G | 10 | a0001c0002t0001g0009a0001c0002t0001g0027a0001c0002t0001g0062others(7): Show | 14 | HG01069.hp2 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.60+4351A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244057 | ||||||
chr12:69244067
|
T | C | 223 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(220): Show | 292 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.60+4361T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244067 | ||||||
chr12:69244121
|
G | T | 1 | a0001c0001t0034g0094 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.60+4415G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244121 | ||||||
chr12:69244302
|
C | G | 23 | a0001c0001t0005g0003a0001c0001t0005g0017a0001c0001t0005g0018others(20): Show | 34 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.60+4596C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244302 | ||||||
chr12:69244396
|
G | C | 1 | a0001c0001t0027g0045 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.60+4690G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244396 | ||||||
chr12:69244459
|
A | G | 1 | a0001c0002t0001g0093 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.60+4753A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244459 | ||||||
chr12:69244518
|
T | C | 172 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(169): Show | 228 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.60+4812T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244518 | ||||||
chr12:69244638
|
C | T | 1 | a0001c0001t0055g0264 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.60+4932C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244638 | ||||||
chr12:69244695
|
CT | C | 173 | a0001c0001t0002g0174a0001c0001t0003g0001a0001c0001t0003g0020others(170): Show | 229 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.60+5000delT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69244695 | |||||
chr12:69244780
|
G | C | 1 | a0001c0001t0063g0057 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.60+5074G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244780 | ||||||
chr12:69244830
|
T | C | 223 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(220): Show | 292 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.60+5124T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244830 | ||||||
chr12:69245096
|
TA | T | 53 | a0001c0001t0002g0041a0001c0001t0002g0170a0001c0001t0002g0215others(50): Show | 67 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.60+5408delA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69245096 | |||||
chr12:69245096
|
TAA | T | 121 | a0001c0001t0005g0239a0001c0002t0001g0009a0001c0002t0001g0014others(118): Show | 149 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.60+5407_60+5408del others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69245096 | |||||
chr12:69245098
|
A | T | 1 | a0001c0001t0018g0240 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.60+5392A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245098 | ||||||
chr12:69245149
|
A | G | 42 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(39): Show | 68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.60+5443A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245149 | ||||||
chr12:69245215
|
T | C | 2 | a0001c0002t0001g0027a0001c0002t0001g0089 | 3 | HG02647.hp2 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.60+5509T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245215 | ||||||
chr12:69245271
|
G | A | 1 | a0001c0001t0031g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.60+5565G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245271 | ||||||
chr12:69245295
|
C | T | 1 | a0001c0002t0001g0156 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.60+5589C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245295 | ||||||
chr12:69245365
|
C | G | 23 | a0001c0001t0005g0003a0001c0001t0005g0017a0001c0001t0005g0018others(20): Show | 34 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.60+5659C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245365 | ||||||
chr12:69245427
|
G | A | 223 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(220): Show | 292 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.61-5702G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245427 | ||||||
chr12:69245435
|
A | G | 223 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(220): Show | 292 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.61-5694A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245435 | ||||||
chr12:69245458
|
T | G | 172 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(169): Show | 228 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.61-5671T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245458 | ||||||
chr12:69245805
|
G | A | 1 | a0001c0002t0001g0099 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.61-5324G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245805 | ||||||
chr12:69245879
|
A | G | 7 | a0001c0001t0014g0262a0001c0001t0014g0265a0001c0001t0019g0019others(4): Show | 8 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-5250A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245879 | ||||||
chr12:69245899
|
A | G | 23 | a0001c0001t0005g0003a0001c0001t0005g0017a0001c0001t0005g0018others(20): Show | 34 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.61-5230A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245899 | ||||||
chr12:69246055
|
C | A | 1 | a0001c0002t0081g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.61-5074C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246055 | ||||||
chr12:69246165
|
G | C | 1 | a0001c0001t0020g0229 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.61-4964G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246165 | ||||||
chr12:69246264
|
A | G | 1 | a0001c0001t0040g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.61-4865A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246264 | ||||||
chr12:69246321
|
T | C | 1 | a0001c0001t0002g0187 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.61-4808T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246321 | ||||||
chr12:69246526
|
A | G | 1 | a0001c0001t0073g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.61-4603A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246526 | ||||||
chr12:69246704
|
C | T | 1 | a0001c0001t0003g0081 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.61-4425C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246704 | ||||||
chr12:69246721
|
C | G | 41 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(38): Show | 66 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.61-4408C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246721 | ||||||
chr12:69246800
|
T | C | 1 | a0001c0001t0002g0246 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.61-4329T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246800 | ||||||
chr12:69246816
|
A | G | 1 | a0001c0001t0085g0080 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.61-4313A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246816 | ||||||
chr12:69246876
|
C | T | 1 | a0001c0001t0033g0186 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.61-4253C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246876 | ||||||
chr12:69247093
|
A | G | 1 | a0001c0001t0058g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.61-4036A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69247093 | ||||||
chr12:69247122
|
G | GA | 171 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(168): Show | 227 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.61-4001dupA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69247122 | |||||
chr12:69247134
|
A | G | 10 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0007g0038others(7): Show | 11 | HG00597.hp1 HG00621.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.61-3995A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69247134 | ||||||
chr12:69247207
|
A | G | 1 | a0001c0001t0073g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.61-3922A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69247207 | ||||||
chr12:69247336
|
T | C | 1 | a0001c0001t0063g0057 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.61-3793T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69247336 | ||||||
chr12:69247369
|
G | GT | 18 | a0001c0001t0002g0036a0001c0001t0002g0060a0001c0001t0002g0205others(15): Show | 21 | HG00408.hp1 HG01175.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.61-3746dupT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69247369 | |||||
chr12:69247369
|
G | GTT | 9 | a0001c0001t0002g0016a0001c0001t0002g0037a0001c0001t0002g0170others(6): Show | 10 | HG00735.hp2 HG02083.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-3747_61-3746dup others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69247369 | |||||
chr12:69247369
|
G | T | 2 | a0001c0001t0029g0227a0001c0001t0029g0228 | 2 | HG00738.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.61-3760G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69247369 | ||||||
chr12:69247369
|
GT | G | 12 | a0001c0001t0002g0250a0001c0001t0014g0262a0001c0001t0014g0265others(9): Show | 15 | HG00733.hp2 HG01070.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.61-3746delT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69247369 | |||||
chr12:69247449
|
ACAG | A | 41 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(38): Show | 66 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.61-3676_61-3674del others(3): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69247449 | |||||
chr12:69247479
|
T | G | 2 | a0001c0002t0004g0101a0001c0002t0004g0102 | 2 | HG00438.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.61-3650T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69247479 | ||||||
chr12:69247513
|
C | A | 2 | a0001c0001t0029g0227a0001c0001t0029g0228 | 2 | HG00738.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.61-3616C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69247513 | ||||||
chr12:69247567
|
G | A | 1 | a0001c0001t0045g0188 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.61-3562G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69247567 | ||||||
chr12:69247594
|
T | C | 4 | a0001c0001t0031g0256a0001c0001t0064g0242a0001c0004t0013g0222others(1): Show | 4 | HG02486.hp1 HG02486.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-3535T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69247594 | ||||||
chr12:69247796
|
T | TAA | 3 | a0001c0001t0010g0023a0001c0001t0010g0065a0001c0001t0042g0079 | 4 | NA18988.hp1 NA19006.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-3330_61-3329dup others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69247796 | |||||
chr12:69248035
|
C | T | 3 | a0001c0002t0004g0101a0001c0002t0004g0102a0001c0002t0004g0155 | 3 | HG00438.hp1 HG02132.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.61-3094C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248035 | ||||||
chr12:69248365
|
G | T | 3 | a0001c0002t0001g0153a0001c0002t0001g0154a0001c0002t0076g0152 | 3 | HG01106.hp1 HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.61-2764G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248365 | ||||||
chr12:69248505
|
T | A | 2 | a0001c0001t0013g0042a0001c0001t0021g0042 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.61-2624T>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248505 | ||||||
chr12:69248535
|
C | T | 226 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(223): Show | 295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.61-2594C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248535 | ||||||
chr12:69248653
|
G | A | 1 | a0001c0001t0007g0171 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.61-2476G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248653 | ||||||
chr12:69248860
|
A | G | 1 | a0001c0001t0063g0057 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.61-2269A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248860 | ||||||
chr12:69248865
|
C | T | 1 | a0001c0001t0014g0265 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.61-2264C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248865 | ||||||
chr12:69248866
|
G | A | 2 | a0001c0001t0019g0019a0001c0001t0050g0019 | 3 | HG01167.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.61-2263G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248866 | ||||||
chr12:69248903
|
A | T | 222 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(219): Show | 291 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.61-2226A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248903 | ||||||
chr12:69248964
|
C | T | 2 | a0001c0001t0007g0173a0001c0004t0013g0245 | 2 | HG02486.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.61-2165C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248964 | ||||||
chr12:69248968
|
C | T | 1 | a0001c0001t0064g0242 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.61-2161C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248968 | ||||||
chr12:69249012
|
C | T | 42 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(39): Show | 68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.61-2117C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249012 | ||||||
chr12:69249013
|
G | A | 1 | a0001c0001t0022g0204 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.61-2116G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249013 | ||||||
chr12:69249021
|
C | T | 7 | a0001c0001t0013g0042a0001c0001t0013g0052a0001c0001t0013g0231others(4): Show | 7 | HG02055.hp1 HG02818.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-2108C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249021 | ||||||
chr12:69249092
|
CTACAAAA others(2): Show |
C | 8 | a0001c0001t0002g0215a0001c0001t0009g0011a0001c0001t0009g0201others(5): Show | 10 | HG02056.hp2 NA18971.hp2 NA18979.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-2031_61-2023del others(9): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249092 | |||||
chr12:69249133
|
G | A | 172 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(169): Show | 228 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.61-1996G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249133 | ||||||
chr12:69249151
|
TC | T | 8 | a0001c0001t0005g0003a0001c0001t0005g0235a0001c0001t0005g0236others(5): Show | 17 | HG00323.hp1 HG00544.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.61-1977delC | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249151 | ||||||
chr12:69249151
|
TCG | T | 8 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0232others(5): Show | 10 | HG00280.hp1 HG00738.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.61-1977_61-1976del others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249151 | ||||||
chr12:69249151
|
TCGGGGGG others(4): Show |
T | 42 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(39): Show | 68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.61-1977_61-1967del others(11): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249151 | ||||||
chr12:69249152
|
C | CGGG | 22 | a0001c0001t0002g0044a0001c0001t0002g0048a0001c0001t0002g0050others(19): Show | 25 | HG00558.hp2 HG00639.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.61-1962_61-1960dup others(3): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | |||||
chr12:69249152
|
C | CGGGG | 16 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0040others(13): Show | 21 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.61-1963_61-1960dup others(4): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | |||||
chr12:69249152
|
C | CGGGGGGG others(3): Show |
2 | a0001c0001t0009g0202a0001c0001t0020g0179 | 2 | HG02056.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.61-1969_61-1960dup others(10): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | |||||
chr12:69249152
|
C | CGGGGGGG others(5): Show |
2 | a0001c0001t0044g0257a0001c0001t0057g0226 | 2 | NA19043.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.61-1971_61-1960dup others(12): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | |||||
chr12:69249152
|
C | CGGTGGGG others(3): Show |
13 | a0001c0002t0001g0029a0001c0002t0001g0093a0001c0002t0001g0112others(10): Show | 14 | HG00558.hp1 HG01891.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(10): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | |||||
chr12:69249152
|
C | CGGTGGGG others(4): Show |
10 | a0001c0002t0001g0014a0001c0002t0001g0089a0001c0002t0001g0090others(7): Show | 11 | HG01168.hp1 HG01346.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(11): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | |||||
chr12:69249152
|
C | CGGTGGGG others(5): Show |
8 | a0001c0002t0001g0091a0001c0002t0001g0118a0001c0002t0001g0153others(5): Show | 8 | HG00609.hp1 HG00673.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(12): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | |||||
chr12:69249152
|
C | CGGTGGGG others(6): Show |
18 | a0001c0002t0001g0049a0001c0002t0001g0092a0001c0002t0001g0099others(15): Show | 18 | HG00408.hp1 HG01106.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(13): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | |||||
chr12:69249152
|
C | CGGTGGGG others(7): Show |
14 | a0001c0002t0001g0054a0001c0002t0001g0095a0001c0002t0001g0127others(11): Show | 14 | HG00609.hp2 HG01258.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(14): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | |||||
chr12:69249152
|
C | CGGTGGGG others(8): Show |
6 | a0001c0002t0001g0046a0001c0002t0001g0134a0001c0002t0001g0136others(3): Show | 6 | HG00735.hp1 HG01069.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(15): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | |||||
chr12:69249152
|
C | CGGTGGGG others(9): Show |
5 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0055others(2): Show | 7 | HG01099.hp1 HG01175.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(16): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | |||||
chr12:69249152
|
C | CGGTGGGG others(10): Show |
8 | a0001c0002t0001g0140a0001c0002t0001g0141a0001c0002t0001g0144others(5): Show | 8 | HG01071.hp2 HG02135.hp2 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(17): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | |||||
chr12:69249152
|
C | CGGTGGGG others(11): Show |
4 | a0001c0002t0001g0034a0001c0002t0001g0146a0001c0002t0001g0147others(1): Show | 4 | HG01952.hp2 NA18954.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(18): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | |||||
chr12:69249152
|
C | CGGTGGGG others(12): Show |
1 | a0001c0002t0001g0148 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.61-1975_61-1974ins others(19): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | |||||
chr12:69249152
|
C | CGGTGGGG others(17): Show |
1 | a0001c0002t0001g0149 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.61-1975_61-1974ins others(24): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | |||||
chr12:69249152
|
C | CGGTGGGG others(18): Show |
1 | a0001c0002t0025g0150 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.61-1975_61-1974ins others(25): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | |||||
chr12:69249152
|
C | CGGTGGGG others(28): Show |
1 | a0001c0002t0001g0151 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.61-1975_61-1974ins others(35): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | |||||
chr12:69249152
|
C | G | 6 | a0001c0001t0002g0200a0001c0001t0005g0238a0001c0001t0007g0172others(3): Show | 6 | HG00733.hp1 HG00741.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-1977C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249152 | ||||||
chr12:69249154
|
G | GT | 6 | a0001c0002t0004g0004a0001c0002t0004g0098a0001c0002t0004g0102others(3): Show | 11 | HG00597.hp2 HG00621.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(1): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249154 | ||||||
chr12:69249155
|
G | T | 10 | a0001c0002t0001g0110a0001c0002t0004g0002a0001c0002t0004g0035others(7): Show | 21 | HG00438.hp1 HG02027.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.61-1974G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249155 | ||||||
chr12:69249156
|
G | A | 3 | a0001c0001t0002g0036a0001c0001t0002g0205a0001c0001t0002g0216 | 4 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-1973G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249156 | ||||||
chr12:69249157
|
G | T | 1 | a0001c0002t0001g0108 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.61-1972G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249157 | ||||||
chr12:69249161
|
G | T | 2 | a0001c0001t0013g0042a0001c0001t0021g0042 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.61-1968G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249161 | ||||||
chr12:69249163
|
G | C | 2 | a0001c0001t0033g0185a0001c0001t0033g0186 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.61-1966G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249163 | ||||||
chr12:69249163
|
G | GGGGGGGG others(8): Show |
1 | a0001c0001t0002g0174 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.61-1960_61-1959ins others(15): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249163 | |||||
chr12:69249163
|
G | T | 42 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(39): Show | 68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.61-1966G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249163 | ||||||
chr12:69249167
|
G | A | 42 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(39): Show | 68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.61-1962G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249167 | ||||||
chr12:69249168
|
G | C | 128 | a0001c0001t0005g0003a0001c0001t0005g0017a0001c0001t0005g0018others(125): Show | 167 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.61-1961G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249168 | ||||||
chr12:69249188
|
G | A | 2 | a0001c0004t0013g0222a0001c0004t0013g0245 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.61-1941G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249188 | ||||||
chr12:69249255
|
AG | A | 3 | a0001c0001t0011g0192a0001c0001t0011g0198a0001c0001t0011g0214 | 3 | HG00639.hp2 HG00741.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.61-1873delG | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249255 | ||||||
chr12:69249257
|
C | T | 3 | a0001c0001t0011g0192a0001c0001t0011g0198a0001c0001t0011g0214 | 3 | HG00639.hp2 HG00741.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.61-1872C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249257 | ||||||
chr12:69249266
|
G | A | 3 | a0001c0001t0003g0066a0001c0004t0013g0222a0001c0004t0013g0245 | 3 | HG02083.hp2 HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.61-1863G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249266 | ||||||
chr12:69249282
|
TAAATAA | T | 13 | a0001c0001t0013g0052a0001c0001t0020g0177a0001c0001t0020g0179others(10): Show | 13 | HG02572.hp2 HG02723.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.61-1842_61-1837del others(6): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249282 | |||||
chr12:69249287
|
A | T | 17 | a0001c0001t0005g0003a0001c0001t0005g0017a0001c0001t0005g0018others(14): Show | 28 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.61-1842A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249287 | ||||||
chr12:69249293
|
T | A | 2 | a0001c0001t0002g0036a0001c0001t0002g0216 | 3 | HG02809.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.61-1836T>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249293 | ||||||
chr12:69249353
|
A | G | 1 | a0001c0001t0022g0217 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.61-1776A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249353 | ||||||
chr12:69249371
|
A | G | 2 | a0001c0002t0035g0138a0001c0002t0035g0145 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.61-1758A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249371 | ||||||
chr12:69249377
|
T | A | 1 | a0001c0001t0030g0178 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.61-1752T>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249377 | ||||||
chr12:69249426
|
T | TTC | 304 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(301): Show | 389 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(386): Show |
intron_variant | MODIFIER | c.61-1701_61-1700dup others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249426 | |||||
chr12:69249495
|
G | C | 4 | a0001c0001t0031g0219a0001c0001t0031g0256a0001c0001t0065g0203others(1): Show | 4 | HG02109.hp2 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-1634G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249495 | ||||||
chr12:69249541
|
C | T | 172 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(169): Show | 228 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.61-1588C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249541 | ||||||
chr12:69249747
|
G | A | 7 | a0001c0002t0012g0005a0001c0002t0012g0083a0001c0002t0036g0012others(4): Show | 12 | HG01361.hp2 HG01884.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.61-1382G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249747 | ||||||
chr12:69249809
|
A | G | 1 | a0001c0002t0001g0133 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.61-1320A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249809 | ||||||
chr12:69250030
|
A | G | 1 | a0001c0001t0027g0045 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.61-1099A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250030 | ||||||
chr12:69250099
|
CATTT | C | 3 | a0001c0001t0077g0013a0001c0001t0078g0013a0001c0001t0079g0013 | 3 | HG00639.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.61-1026_61-1023del others(4): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69250099 | |||||
chr12:69250109
|
G | A | 2 | a0001c0002t0001g0095a0001c0002t0001g0133 | 2 | HG00609.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.61-1020G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250109 | ||||||
chr12:69250171
|
T | C | 1 | a0001c0001t0085g0080 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.61-958T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250171 | ||||||
chr12:69250205
|
A | T | 6 | a0001c0001t0031g0219a0001c0001t0031g0256a0001c0001t0033g0185others(3): Show | 6 | HG02109.hp2 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-924A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250205 | ||||||
chr12:69250271
|
G | A | 31 | a0001c0001t0005g0003a0001c0001t0005g0017a0001c0001t0005g0018others(28): Show | 42 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.61-858G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250271 | ||||||
chr12:69250416
|
C | T | 1 | a0001c0001t0002g0187 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.61-713C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250416 | ||||||
chr12:69250483
|
G | A | 1 | a0001c0001t0003g0067 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.61-646G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250483 | ||||||
chr12:69250520
|
G | A | 6 | a0001c0002t0001g0034a0001c0002t0001g0134a0001c0002t0001g0140others(3): Show | 6 | NA18947.hp1 NA18954.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-609G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250520 | ||||||
chr12:69250561
|
G | A | 1 | a0001c0001t0027g0045 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.61-568G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250561 | ||||||
chr12:69250590
|
C | CA | 18 | a0001c0001t0002g0037a0001c0001t0002g0048a0001c0001t0002g0050others(15): Show | 18 | HG00639.hp2 HG00741.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.61-522dupA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69250590 | |||||
chr12:69250590
|
CA | C | 27 | a0001c0001t0013g0042a0001c0001t0013g0052a0001c0001t0013g0231others(24): Show | 28 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.61-522delA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69250590 | |||||
chr12:69250603
|
A | G | 6 | a0001c0001t0014g0262a0001c0001t0014g0265a0001c0001t0019g0019others(3): Show | 7 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.61-526A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250603 | ||||||
chr12:69250608
|
GAAAA | G | 118 | a0001c0002t0001g0009a0001c0002t0001g0014a0001c0002t0001g0027others(115): Show | 146 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.61-516_61-513delAA others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69250608 | |||||
chr12:69250612
|
A | G | 5 | a0001c0002t0001g0114a0001c0002t0001g0132a0001c0002t0001g0137others(2): Show | 5 | HG01433.hp2 HG01981.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-517A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250612 | ||||||
chr12:69250655
|
G | T | 1 | a0001c0001t0002g0251 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.61-474G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250655 | ||||||
chr12:69250655
|
GT | G | 222 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(219): Show | 291 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.61-465delT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69250655 | |||||
chr12:69250831
|
G | A | 3 | a0001c0001t0002g0036a0001c0001t0002g0205a0001c0001t0002g0216 | 4 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-298G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250831 | ||||||
chr12:69251023
|
C | T | 1 | a0001c0001t0027g0045 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.61-106C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69251023 | ||||||
chr12:69251401
|
A | C | 1 | a0001c0001t0052g0209 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.270+63A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69251401 | ||||||
chr12:69251449
|
A | G | 2 | a0001c0001t0019g0019a0001c0001t0050g0019 | 3 | HG01167.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.270+111A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69251449 | ||||||
chr12:69251455
|
G | T | 53 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0049others(50): Show | 54 | HG00408.hp2 HG00673.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.270+117G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69251455 | ||||||
chr12:69251459
|
G | T | 1 | a0001c0001t0020g0179 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.270+121G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69251459 | ||||||
chr12:69251605
|
T | C | 9 | a0001c0001t0013g0042a0001c0001t0013g0052a0001c0001t0013g0231others(6): Show | 9 | HG02055.hp1 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.270+267T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69251605 | ||||||
chr12:69251786
|
T | C | 31 | a0001c0001t0005g0003a0001c0001t0005g0017a0001c0001t0005g0018others(28): Show | 42 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.270+448T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69251786 | ||||||
chr12:69251818
|
C | T | 43 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(40): Show | 69 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.270+480C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69251818 | ||||||
chr12:69251960
|
A | G | 1 | a0001c0004t0013g0245 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.270+622A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69251960 | ||||||
chr12:69252059
|
C | CG | 3 | a0001c0002t0012g0005a0001c0002t0012g0083a0001c0002t0072g0005 | 7 | HG01361.hp2 HG01884.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.270+722dupG | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 69252059 | |||||
chr12:69252083
|
C | T | 2 | a0001c0001t0032g0183a0001c0001t0032g0184 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.270+745C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252083 | ||||||
chr12:69252084
|
A | G | 226 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(223): Show | 295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.270+746A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252084 | ||||||
chr12:69252140
|
T | A | 1 | a0001c0001t0064g0242 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.270+802T>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252140 | ||||||
chr12:69252143
|
T | C | 1 | a0001c0002t0001g0103 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.270+805T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252143 | ||||||
chr12:69252230
|
T | C | 226 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(223): Show | 295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.271-821T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252230 | ||||||
chr12:69252253
|
C | CAAAA | 218 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(215): Show | 287 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.271-795_271-794ins others(4): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 69252253 | |||||
chr12:69252253
|
C | CAAAAA | 8 | a0001c0001t0013g0042a0001c0001t0013g0052a0001c0001t0013g0231others(5): Show | 8 | HG02055.hp1 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-795_271-794ins others(5): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 69252253 | |||||
chr12:69252377
|
A | G | 7 | a0001c0001t0014g0262a0001c0001t0014g0265a0001c0001t0019g0019others(4): Show | 8 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.271-674A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252377 | ||||||
chr12:69252537
|
G | A | 1 | a0001c0001t0002g0247 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.271-514G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252537 | ||||||
chr12:69252568
|
T | C | 1 | a0001c0001t0027g0045 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.271-483T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252568 | ||||||
chr12:69252631
|
A | G | 2 | a0001c0001t0003g0020a0001c0001t0040g0077 | 3 | NA18960.hp1 NA18963.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.271-420A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252631 | ||||||
chr12:69252912
|
C | G | 8 | a0001c0001t0013g0042a0001c0001t0013g0052a0001c0001t0013g0231others(5): Show | 8 | HG02055.hp1 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-139C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252912 | ||||||
chr12:69253340
|
C | G | 1 | a0001c0001t0063g0057 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.374+186C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69253340 | ||||||
chr12:69253362
|
G | C | 3 | a0001c0001t0007g0171a0001c0001t0007g0172a0001c0001t0007g0173 | 3 | HG02027.hp1 HG02523.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.374+208G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69253362 | ||||||
chr12:69253461
|
C | A | 3 | a0001c0001t0002g0190a0001c0003t0002g0015a0001c0003t0038g0015 | 4 | HG00558.hp2 NA18975.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.374+307C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69253461 | ||||||
chr12:69253498
|
A | G | 42 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(39): Show | 68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.374+344A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69253498 | ||||||
chr12:69253575
|
A | G | 2 | a0001c0001t0033g0185a0001c0001t0033g0186 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.374+421A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69253575 | ||||||
chr12:69253710
|
A | G | 1 | a0001c0002t0001g0110 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.374+556A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69253710 | ||||||
chr12:69253900
|
T | C | 1 | a0001c0002t0001g0156 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.374+746T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69253900 | ||||||
chr12:69254176
|
G | C | 1 | a0001c0001t0086g0068 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.374+1022G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254176 | ||||||
chr12:69254182
|
C | T | 172 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(169): Show | 228 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.374+1028C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254182 | ||||||
chr12:69254183
|
T | TA | 110 | a0001c0001t0014g0262a0001c0001t0014g0265a0001c0001t0019g0019others(107): Show | 130 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.374+1039dupA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 69254183 | |||||
chr12:69254183
|
TA | T | 29 | a0001c0001t0005g0003a0001c0001t0005g0017a0001c0001t0005g0018others(26): Show | 40 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.374+1039delA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 69254183 | |||||
chr12:69254184
|
A | T | 10 | a0001c0002t0001g0009a0001c0002t0001g0027a0001c0002t0001g0062others(7): Show | 14 | HG01069.hp2 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.374+1030A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254184 | ||||||
chr12:69254185
|
A | T | 1 | a0001c0002t0001g0093 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.374+1031A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254185 | ||||||
chr12:69254301
|
A | C | 2 | a0001c0001t0029g0227a0001c0001t0029g0228 | 2 | HG00738.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.374+1147A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254301 | ||||||
chr12:69254466
|
A | G | 31 | a0001c0001t0005g0003a0001c0001t0005g0017a0001c0001t0005g0018others(28): Show | 42 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.374+1312A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254466 | ||||||
chr12:69254548
|
C | T | 31 | a0001c0001t0005g0003a0001c0001t0005g0017a0001c0001t0005g0018others(28): Show | 42 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.374+1394C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254548 | ||||||
chr12:69254574
|
G | A | 1 | a0001c0001t0047g0234 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.374+1420G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254574 | ||||||
chr12:69254631
|
G | A | 2 | a0001c0001t0033g0185a0001c0001t0033g0186 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.374+1477G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254631 | ||||||
chr12:69254946
|
A | G | 42 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(39): Show | 68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.375-1751A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254946 | ||||||
chr12:69255367
|
A | T | 2 | a0001c0002t0036g0012a0001c0002t0071g0012 | 3 | HG02451.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.375-1330A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69255367 | ||||||
chr12:69255432
|
A | G | 7 | a0001c0002t0012g0005a0001c0002t0012g0083a0001c0002t0036g0012others(4): Show | 12 | HG01361.hp2 HG01884.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.375-1265A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69255432 | ||||||
chr12:69255535
|
A | G | 7 | a0001c0002t0012g0005a0001c0002t0012g0083a0001c0002t0036g0012others(4): Show | 12 | HG01361.hp2 HG01884.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.375-1162A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69255535 | ||||||
chr12:69255606
|
A | T | 1 | a0001c0001t0015g0076 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.375-1091A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69255606 | ||||||
chr12:69255661
|
C | A | 42 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(39): Show | 68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.375-1036C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69255661 | ||||||
chr12:69255723
|
G | C | 1 | a0001c0002t0006g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.375-974G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69255723 | ||||||
chr12:69255790
|
G | GC | 3 | a0001c0002t0012g0005a0001c0002t0012g0083a0001c0002t0072g0005 | 7 | HG01361.hp2 HG01884.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.375-905dupC | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 69255790 | |||||
chr12:69255807
|
G | A | 2 | a0001c0001t0013g0052a0001c0001t0021g0053 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.375-890G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69255807 | ||||||
chr12:69255838
|
C | T | 15 | a0001c0001t0020g0177a0001c0001t0020g0179a0001c0001t0030g0176others(12): Show | 15 | HG02109.hp2 HG02572.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.375-859C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69255838 | ||||||
chr12:69255870
|
T | C | 1 | a0001c0002t0001g0099 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.375-827T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69255870 | ||||||
chr12:69256122
|
A | T | 1 | a0001c0001t0031g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.375-575A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69256122 | ||||||
chr12:69256134
|
A | G | 1 | a0001c0001t0028g0043 | 2 | HG00642.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.375-563A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69256134 | ||||||
chr12:69256343
|
A | G | 42 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(39): Show | 68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.375-354A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69256343 | ||||||
chr12:69256356
|
C | T | 1 | a0001c0001t0008g0075 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.375-341C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69256356 | ||||||
chr12:69256370
|
A | G | 1 | a0001c0001t0003g0074 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.375-327A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69256370 | ||||||
chr12:69257048
|
T | C | 1 | a0001c0002t0004g0128 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.520+206T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 4/9 | chr12 | 69257048 | ||||||
chr12:69257180
|
A | G | 1 | a0001c0002t0069g0122 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.520+338A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 4/9 | chr12 | 69257180 | ||||||
chr12:69257244
|
A | G | 1 | a0001c0001t0004g0073 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.520+402A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 4/9 | chr12 | 69257244 | ||||||
chr12:69257301
|
G | C | 2 | a0001c0001t0020g0177a0001c0001t0020g0179 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.521-431G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 4/9 | chr12 | 69257301 | ||||||
chr12:69257396
|
A | T | 5 | a0001c0001t0013g0042a0001c0001t0013g0231a0001c0001t0020g0229others(2): Show | 5 | HG02055.hp1 HG02818.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.521-336A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 4/9 | chr12 | 69257396 | ||||||
chr12:69257397
|
C | T | 4 | a0001c0001t0031g0219a0001c0001t0031g0256a0001c0001t0065g0203others(1): Show | 4 | HG02109.hp2 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.521-335C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 4/9 | chr12 | 69257397 | ||||||
chr12:69257405
|
G | A | 1 | a0001c0001t0027g0045 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.521-327G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 4/9 | chr12 | 69257405 | ||||||
chr12:69257413
|
C | A | 2 | a0001c0001t0019g0261a0001c0001t0049g0263 | 2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.521-319C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 4/9 | chr12 | 69257413 | ||||||
chr12:69257416
|
A | C | 15 | a0001c0001t0020g0177a0001c0001t0020g0179a0001c0001t0030g0176others(12): Show | 15 | HG02109.hp2 HG02572.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.521-316A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 4/9 | chr12 | 69257416 | ||||||
chr12:69257920
|
A | G | 1 | a0001c0002t0001g0131 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.694+15A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 5/9 | chr12 | 69257920 | ||||||
chr12:69258358
|
T | C | 2 | a0001c0001t0065g0203a0001c0001t0066g0181 | 2 | HG02109.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.695-232T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 5/9 | chr12 | 69258358 | ||||||
chr12:69258434
|
T | C | 1 | a0001c0002t0001g0046 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.695-156T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 5/9 | chr12 | 69258434 | ||||||
chr12:69258435
|
G | A | 1 | a0001c0002t0068g0085 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.695-155G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 5/9 | chr12 | 69258435 | ||||||
chr12:69258556
|
G | GT | 224 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(221): Show | 293 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.695-25dupT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr12 | 69258556 | |||||
chr12:69259104
|
T | C | 1 | a0001c0001t0043g0022 | 2 | HG02145.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1199+10T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 6/9 | chr12 | 69259104 | ||||||
chr12:69259292
|
A | C | 1 | a0001c0001t0009g0218 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1200-136A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 6/9 | chr12 | 69259292 | ||||||
chr12:69259366
|
T | C | 173 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(170): Show | 229 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.1200-62T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 6/9 | chr12 | 69259366 | ||||||
chr12:69259600
|
A | G | 7 | a0001c0001t0020g0177a0001c0001t0020g0179a0001c0001t0030g0176others(4): Show | 7 | HG02723.hp2 HG02976.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1315+57A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 7/9 | chr12 | 69259600 | ||||||
chr12:69259608
|
T | C | 1 | a0001c0001t0051g0175 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1315+65T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 7/9 | chr12 | 69259608 | ||||||
chr12:69259732
|
A | T | 2 | a0001c0001t0002g0170a0001c0001t0002g0208 | 2 | NA18986.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1315+189A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 7/9 | chr12 | 69259732 | ||||||
chr12:69259749
|
A | T | 1 | a0001c0002t0006g0163 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1315+206A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 7/9 | chr12 | 69259749 | ||||||
chr12:69259906
|
A | G | 6 | a0001c0001t0020g0177a0001c0001t0020g0179a0001c0001t0030g0176others(3): Show | 6 | HG02723.hp2 HG02976.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1316-138A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 7/9 | chr12 | 69259906 | ||||||
chr12:69259996
|
T | G | 7 | a0001c0002t0001g0034a0001c0002t0001g0126a0001c0002t0001g0134others(4): Show | 7 | NA18947.hp1 NA18954.hp2 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.1316-48T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 7/9 | chr12 | 69259996 | ||||||
chr12:69260287
|
T | A | 1 | a0001c0001t0009g0202 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1469+90T>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69260287 | ||||||
chr12:69260319
|
G | GT | 61 | a0001c0001t0002g0036a0001c0001t0002g0197a0001c0001t0002g0205others(58): Show | 92 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1469+133dupT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 69260319 | |||||
chr12:69260319
|
G | GTT | 120 | a0001c0002t0001g0009a0001c0002t0001g0014a0001c0002t0001g0027others(117): Show | 148 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1469+132_1469+133d others(4): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 69260319 | |||||
chr12:69260323
|
T | G | 1 | a0001c0001t0028g0043 | 2 | HG00642.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1469+126T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69260323 | ||||||
chr12:69260335
|
C | A | 1 | a0001c0001t0065g0203 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1469+138C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69260335 | ||||||
chr12:69260336
|
T | G | 1 | a0001c0001t0065g0203 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1469+139T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69260336 | ||||||
chr12:69260407
|
A | G | 124 | a0001c0002t0001g0009a0001c0002t0001g0014a0001c0002t0001g0027others(121): Show | 152 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.1469+210A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69260407 | ||||||
chr12:69260526
|
T | C | 6 | a0001c0001t0014g0262a0001c0001t0014g0265a0001c0001t0019g0019others(3): Show | 7 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1469+329T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69260526 | ||||||
chr12:69260560
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1469+363G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69260560 | ||||||
chr12:69260607
|
C | T | 1 | a0001c0001t0005g0235 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1469+410C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69260607 | ||||||
chr12:69260656
|
G | A | 2 | a0001c0002t0001g0123a0001c0002t0001g0129 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1469+459G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69260656 | ||||||
chr12:69261038
|
T | C | 1 | a0001c0001t0003g0069 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1469+841T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69261038 | ||||||
chr12:69261179
|
C | T | 6 | a0001c0001t0020g0177a0001c0001t0020g0179a0001c0001t0030g0176others(3): Show | 6 | HG02723.hp2 HG02976.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1469+982C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69261179 | ||||||
chr12:69261186
|
C | A | 1 | a0001c0001t0064g0242 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1469+989C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69261186 | ||||||
chr12:69261275
|
CT | C | 2 | a0001c0002t0036g0012a0001c0002t0071g0012 | 3 | HG02451.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1469+1083delT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 69261275 | |||||
chr12:69261336
|
G | A | 2 | a0001c0001t0013g0231a0001c0001t0021g0230 | 2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1470-1037G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69261336 | ||||||
chr12:69261387
|
A | G | 210 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(207): Show | 279 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.1470-986A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69261387 | ||||||
chr12:69261434
|
G | A | 1 | a0001c0002t0001g0149 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1470-939G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69261434 | ||||||
chr12:69261500
|
G | GGATGAAA others(62): Show |
2 | a0001c0004t0013g0222a0001c0004t0013g0245 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1470-872_1470-804d others(71): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 69261500 | |||||
chr12:69261596
|
G | A | 1 | a0001c0002t0001g0151 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1470-777G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69261596 | ||||||
chr12:69261664
|
T | G | 3 | a0001c0001t0011g0192a0001c0001t0011g0198a0001c0001t0011g0214 | 3 | HG00639.hp2 HG00741.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1470-709T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69261664 | ||||||
chr12:69261852
|
C | T | 2 | a0001c0001t0019g0261a0001c0001t0049g0263 | 2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1470-521C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69261852 | ||||||
chr12:69262122
|
T | TA | 171 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(168): Show | 227 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.1470-249dupA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 69262122 | |||||
chr12:69262320
|
T | C | 1 | a0001c0001t0015g0070 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1470-53T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69262320 | ||||||
chr12:69262322
|
T | G | 3 | a0001c0002t0006g0160a0001c0002t0006g0161a0001c0002t0006g0164 | 3 | NA18959.hp1 NA18964.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1470-51T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69262322 | ||||||
chr12:69262985
|
A | C | 9 | a0001c0001t0002g0016a0001c0001t0002g0037a0001c0001t0002g0170others(6): Show | 10 | HG00735.hp2 HG02083.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.*3+423A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69262985 | ||||||
chr12:69263030
|
A | G | 2 | a0001c0001t0002g0191a0001c0001t0002g0196 | 2 | HG01123.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.*3+468A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69263030 | ||||||
chr12:69263096
|
AT | A | 222 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(219): Show | 291 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.*3+545delT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69263096 | |||||
chr12:69263098
|
T | A | 41 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(38): Show | 67 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.*3+536T>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69263098 | ||||||
chr12:69263365
|
G | A | 225 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(222): Show | 294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.*3+803G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69263365 | ||||||
chr12:69263528
|
T | C | 1 | a0001c0002t0001g0141 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.*3+966T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69263528 | ||||||
chr12:69263651
|
G | A | 1 | a0001c0002t0006g0163 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.*3+1089G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69263651 | ||||||
chr12:69263659
|
A | G | 1 | a0001c0001t0059g0059 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.*3+1097A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69263659 | ||||||
chr12:69263947
|
C | T | 1 | a0001c0002t0001g0156 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.*3+1385C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69263947 | ||||||
chr12:69264193
|
G | A | 2 | a0001c0001t0030g0176a0001c0001t0030g0178 | 2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.*3+1631G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69264193 | ||||||
chr12:69264371
|
A | G | 1 | a0001c0001t0005g0233 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.*3+1809A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69264371 | ||||||
chr12:69264381
|
T | C | 3 | a0001c0001t0023g0010a0001c0001t0051g0175a0001c0001t0070g0010 | 5 | HG00733.hp2 HG01070.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.*3+1819T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69264381 | ||||||
chr12:69264550
|
T | C | 105 | a0001c0002t0001g0014a0001c0002t0001g0028a0001c0002t0001g0029others(102): Show | 124 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.*3+1988T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69264550 | ||||||
chr12:69264890
|
T | C | 2 | a0001c0001t0002g0044a0001c0001t0002g0249 | 3 | NA18942.hp1 NA18945.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.*3+2328T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69264890 | ||||||
chr12:69264955
|
G | A | 1 | a0001c0001t0007g0211 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.*3+2393G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69264955 | ||||||
chr12:69265090
|
T | G | 1 | a0001c0002t0006g0165 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.*3+2528T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265090 | ||||||
chr12:69265120
|
C | G | 1 | a0001c0001t0002g0174 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.*3+2558C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265120 | ||||||
chr12:69265175
|
C | A | 1 | a0001c0001t0020g0229 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*3+2613C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265175 | ||||||
chr12:69265193
|
A | T | 2 | a0001c0002t0001g0112a0001c0002t0001g0115 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.*3+2631A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265193 | ||||||
chr12:69265234
|
G | A | 1 | a0001c0001t0027g0045 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.*3+2672G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265234 | ||||||
chr12:69265519
|
A | G | 105 | a0001c0002t0001g0014a0001c0002t0001g0028a0001c0002t0001g0029others(102): Show | 124 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.*3+2957A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265519 | ||||||
chr12:69265589
|
A | G | 42 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(39): Show | 68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.*3+3027A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265589 | ||||||
chr12:69265598
|
CT | C | 164 | a0001c0001t0002g0205a0001c0001t0003g0001a0001c0001t0003g0020others(161): Show | 215 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.*3+3057delT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69265598 | |||||
chr12:69265598
|
CTT | C | 51 | a0001c0001t0003g0025a0001c0001t0003g0081a0001c0001t0003g0223others(48): Show | 64 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.*3+3056_*3+3057del others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69265598 | |||||
chr12:69265598
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0007g0212 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.*3+3048_*3+3057del others(10): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69265598 | |||||
chr12:69265657
|
C | T | 1 | a0001c0001t0002g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.*3+3095C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265657 | ||||||
chr12:69265832
|
C | A | 1 | a0001c0005t0001g0135 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.*3+3270C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265832 | ||||||
chr12:69265896
|
G | A | 1 | a0001c0001t0005g0232 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.*3+3334G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265896 | ||||||
chr12:69265898
|
G | A | 31 | a0001c0001t0005g0003a0001c0001t0005g0017a0001c0001t0005g0018others(28): Show | 42 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.*3+3336G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265898 | ||||||
chr12:69266026
|
T | TG | 5 | a0001c0001t0031g0219a0001c0001t0031g0256a0001c0001t0033g0186others(2): Show | 5 | HG02109.hp2 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.*3+3465dupG | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69266026 | |||||
chr12:69266027
|
GA | G | 47 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(44): Show | 74 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.*4-3470delA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69266027 | |||||
chr12:69266027
|
GAAAA | G | 127 | a0001c0001t0023g0010a0001c0001t0051g0175a0001c0001t0070g0010others(124): Show | 157 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.*4-3473_*4-3470del others(4): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69266027 | |||||
chr12:69266032
|
A | G | 1 | a0001c0002t0009g0097 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.*3+3470A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69266032 | ||||||
chr12:69266064
|
C | A | 2 | a0001c0002t0001g0027a0001c0002t0001g0089 | 3 | HG02647.hp2 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.*4-3448C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69266064 | ||||||
chr12:69266140
|
C | A | 7 | a0001c0001t0014g0262a0001c0001t0014g0265a0001c0001t0019g0019others(4): Show | 8 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.*4-3372C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69266140 | ||||||
chr12:69266200
|
T | TCTGAGGT others(20): Show |
1 | a0001c0001t0014g0262 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.*4-3308_*4-3282dup others(27): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69266200 | |||||
chr12:69266358
|
T | C | 1 | a0001c0001t0060g0182 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.*4-3154T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69266358 | ||||||
chr12:69266604
|
C | T | 1 | a0001c0001t0022g0217 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.*4-2908C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69266604 | ||||||
chr12:69266765
|
T | G | 1 | a0001c0001t0005g0238 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.*4-2747T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69266765 | ||||||
chr12:69266923
|
T | C | 17 | a0001c0001t0005g0003a0001c0001t0005g0017a0001c0001t0005g0018others(14): Show | 28 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.*4-2589T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69266923 | ||||||
chr12:69266951
|
T | G | 2 | a0001c0001t0033g0185a0001c0001t0033g0186 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.*4-2561T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69266951 | ||||||
chr12:69267036
|
A | G | 2 | a0001c0001t0013g0052a0001c0001t0021g0053 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.*4-2476A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69267036 | ||||||
chr12:69267099
|
G | T | 1 | a0001c0002t0001g0117 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.*4-2413G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69267099 | ||||||
chr12:69267351
|
A | G | 171 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(168): Show | 227 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.*4-2161A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69267351 | ||||||
chr12:69267404
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.*4-2108T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69267404 | ||||||
chr12:69267647
|
C | T | 2 | a0001c0001t0019g0019a0001c0001t0050g0019 | 3 | HG01167.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.*4-1865C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69267647 | ||||||
chr12:69267789
|
A | G | 2 | a0001c0002t0001g0123a0001c0002t0001g0129 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.*4-1723A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69267789 | ||||||
chr12:69267810
|
T | C | 1 | a0001c0001t0053g0199 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.*4-1702T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69267810 | ||||||
chr12:69267933
|
G | A | 1 | a0001c0001t0032g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.*4-1579G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69267933 | ||||||
chr12:69268038
|
G | T | 1 | a0001c0001t0013g0231 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.*4-1474G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69268038 | ||||||
chr12:69268107
|
T | C | 4 | a0001c0001t0019g0019a0001c0001t0019g0261a0001c0001t0049g0263others(1): Show | 5 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.*4-1405T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69268107 | ||||||
chr12:69268476
|
ACT | A | 41 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(38): Show | 67 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.*4-1033_*4-1032del others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69268476 | |||||
chr12:69268581
|
CCTTCTGC others(3): Show |
C | 1 | a0001c0002t0001g0126 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.*4-927_*4-918delCT others(8): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69268581 | |||||
chr12:69268714
|
A | T | 1 | a0001c0001t0002g0200 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.*4-798A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69268714 | ||||||
chr12:69269074
|
T | C | 2 | a0001c0002t0036g0012a0001c0002t0071g0012 | 3 | HG02451.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.*4-438T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69269074 | ||||||
chr12:69269149
|
A | T | 225 | a0001c0001t0003g0001a0001c0001t0003g0020a0001c0001t0003g0024others(222): Show | 294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.*4-363A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69269149 | ||||||
chr12:69269267
|
C | T | 31 | a0001c0001t0005g0003a0001c0001t0005g0017a0001c0001t0005g0018others(28): Show | 42 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.*4-245C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69269267 | ||||||
chr12:69269350
|
A | G | 1 | a0001c0002t0001g0124 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*4-162A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69269350 | ||||||
chr12:69269351
|
C | T | 2 | a0001c0002t0001g0095a0001c0002t0001g0133 | 2 | HG00609.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.*4-161C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69269351 |