geneid | 10898 |
---|---|
ensemblid | ENSG00000160917.15 |
hgncid | 2327 |
symbol | CPSF4 |
name | cleavage and polyadenylation specific factor 4 |
refseq_nuc | NM_006693.4 |
refseq_prot | NP_006684.1 |
ensembl_nuc | ENST00000292476.10 |
ensembl_prot | ENSP00000292476.5 |
mane_status | MANE Select |
chr | chr7 |
start | 99438943 |
end | 99457373 |
strand | + |
ver | v1.2 |
region | chr7:99438943-99457373 |
region5000 | chr7:99433943-99462373 |
regionname0 | CPSF4_chr7_99438943_99457373 |
regionname5000 | CPSF4_chr7_99433943_99462373 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 269 | 364 | 92 | 64 | 152 | 16 | 38 | 116 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 810 | 166 | 62 | 15 | 64 | 5 | 20 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
c0002 | 1/1 | 810 | 166 | 9 | 46 | 81 | 10 | 18 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
c0003 | 0/0 | 810 | 31 | 21 | 2 | 7 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
c0004 | 0/0 | 810 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1014 | 155 | 5 | 44 | 77 | 10 | 17 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
t0002 | 0/0 | 1014 | 95 | 70 | 11 | 7 | 5 | 2 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
t0003 | 0/0 | 1014 | 94 | 7 | 5 | 63 | 1 | 18 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
t0004 | 0/0 | 1014 | 5 | 5 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
t0005 | 0/0 | 1014 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
t0006 | 0/0 | 1014 | 3 | 1 | 2 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
t0007 | 0/0 | 1014 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
t0008 | 0/0 | 1014 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
t0009 | 0/0 | 1014 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
t0010 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
t0011 | 0/0 | 1014 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
t0012 | 0/0 | 1014 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
t0013 | 0/0 | 1014 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 2 | 1 | 4 | 0 | 2 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0002 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0004 | 1/0 | 5 | 0 | 2 | 1 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0006 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0008 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0010 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0022 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 810 | 166 | 62 | 15 | 64 | 5 | 20 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
a0001c0002 | 1/1 | 810 | 166 | 9 | 46 | 81 | 10 | 18 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
a0001c0003 | 0/0 | 810 | 31 | 21 | 2 | 7 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
a0001c0004 | 0/0 | 810 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 1823 | 63 | 46 | 10 | 1 | 4 | 2 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
a0001c0001t0003 | 0/0 | 1823 | 94 | 7 | 5 | 63 | 1 | 18 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
a0001c0001t0004 | 0/0 | 1823 | 5 | 5 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
a0001c0001t0007 | 0/0 | 1823 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
a0001c0001t0010 | 0/0 | 1823 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
a0001c0002t0001 | 1/1 | 1823 | 154 | 5 | 43 | 77 | 10 | 17 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
a0001c0002t0002 | 0/0 | 1823 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
a0001c0002t0005 | 0/0 | 1823 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
a0001c0002t0006 | 0/0 | 1823 | 3 | 1 | 2 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
a0001c0002t0008 | 0/0 | 1823 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
a0001c0002t0011 | 0/0 | 1823 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
a0001c0002t0013 | 0/0 | 1823 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
a0001c0003t0002 | 0/0 | 1823 | 29 | 21 | 1 | 6 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
a0001c0003t0009 | 0/0 | 1823 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
a0001c0003t0012 | 0/0 | 1823 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
a0001c0004t0001 | 0/0 | 1823 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | copy fasta | chr7 | 99433943 | 99462373 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0010 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0001t0010g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0001 | 0/0 | 8 | 1 | 1 | 4 | 0 | 2 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0002 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0004 | 1/0 | 5 | 0 | 2 | 1 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0006 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0022 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0005g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0006g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0006g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0006g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0008g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0011g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0002t0013g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0009g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0003t0012g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
a0001c0004t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0019 | EUR | GBR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00099 | hp2 | a0001 | c0003 | t0002 | g0101 | EUR | GBR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0273 | EUR | FIN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0181 | EUR | FIN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0046 | EUR | FIN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0282 | EUR | FIN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0267 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0287 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0290 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00733 | hp2 | a0001 | c0002 | t0006 | g0295 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00735 | hp1 | a0001 | c0002 | t0008 | g0230 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0232 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0233 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01081 | hp2 | a0001 | c0003 | t0002 | g0095 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0214 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0185 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0292 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0245 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0238 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0209 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01175 | hp2 | a0001 | c0003 | t0009 | g0108 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0150 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01192 | hp2 | a0001 | c0004 | t0001 | g0251 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0274 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0247 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0217 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0195 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01358 | hp2 | a0001 | c0002 | t0006 | g0026 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0135 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0281 | EUR | IBS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0246 | EUR | IBS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0208 | EUR | IBS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0051 | EUR | IBS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0050 | EUR | IBS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0285 | EUR | IBS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0129 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01891 | hp1 | a0001 | c0003 | t0002 | g0091 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0225 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0266 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0152 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0240 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0256 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0229 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02055 | hp2 | a0001 | c0003 | t0002 | g0102 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0293 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0224 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0296 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | CDX | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02165 | hp2 | a0001 | c0002 | t0011 | g0305 | EAS | CDX | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02257 | hp1 | a0001 | c0003 | t0002 | g0097 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02258 | hp1 | a0001 | c0003 | t0002 | g0090 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0297 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0250 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02280 | hp1 | a0001 | c0002 | t0006 | g0001 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0239 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0236 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0270 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0261 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0113 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02523 | hp2 | a0001 | c0003 | t0002 | g0104 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0309 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0177 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02615 | hp1 | a0001 | c0003 | t0002 | g0084 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0114 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0182 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0311 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02647 | hp2 | a0001 | c0003 | t0002 | g0111 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02717 | hp2 | a0001 | c0003 | t0002 | g0110 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0163 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0139 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0278 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02809 | hp1 | a0001 | c0003 | t0002 | g0092 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0140 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0312 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02970 | hp1 | a0001 | c0003 | t0002 | g0089 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0170 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03041 | hp2 | a0001 | c0003 | t0002 | g0096 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0310 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0308 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03195 | hp2 | a0001 | c0001 | t0010 | g0075 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03225 | hp1 | a0001 | c0003 | t0002 | g0082 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0298 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03486 | hp2 | a0001 | c0003 | t0002 | g0099 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03490 | hp1 | a0001 | c0002 | t0013 | g0301 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0159 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0160 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0277 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03516 | hp1 | a0001 | c0002 | t0002 | g0112 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03540 | hp1 | a0001 | c0003 | t0002 | g0106 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03579 | hp2 | a0001 | c0003 | t0002 | g0093 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0023 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0249 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0193 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0248 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0192 | SAS | BEB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0205 | SAS | BEB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0252 | SAS | BEB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0171 | SAS | BEB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0161 | SAS | BEB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0176 | SAS | BEB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0200 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0134 | SAS | BEB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0241 | SAS | BEB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0210 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0149 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0136 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0275 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0024 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18522 | hp1 | a0001 | c0003 | t0002 | g0086 | AFR | YRI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | YRI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | CHB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18906 | hp1 | a0001 | c0003 | t0002 | g0083 | AFR | YRI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | YRI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18939 | hp1 | a0001 | c0003 | t0002 | g0109 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18943 | hp2 | a0001 | c0002 | t0005 | g0304 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18971 | hp1 | a0001 | c0003 | t0002 | g0307 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18982 | hp1 | a0001 | c0002 | t0005 | g0028 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18989 | hp1 | a0001 | c0003 | t0012 | g0300 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18989 | hp2 | a0001 | c0003 | t0002 | g0105 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18997 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19002 | hp2 | a0001 | c0003 | t0002 | g0107 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0288 | AFR | LWK | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | LWK | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | LWK | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | LWK | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19054 | hp2 | a0001 | c0003 | t0002 | g0100 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19062 | hp1 | a0001 | c0002 | t0005 | g0028 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | YRI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA19240 | hp2 | a0001 | c0003 | t0002 | g0087 | AFR | YRI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | TSI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0253 | EUR | TSI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0291 | EUR | TSI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0283 | EUR | TSI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0137 | SAS | GIH | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | GIH | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0212 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02486 | hp1 | a0001 | c0003 | t0002 | g0103 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02559 | hp1 | a0001 | c0001 | t0007 | g0142 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03471 | hp1 | a0001 | c0003 | t0002 | g0098 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG03471 | hp2 | a0001 | c0003 | t0002 | g0094 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG06807 | hp1 | a0001 | c0003 | t0002 | g0088 | AFR | USA | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0279 | AFR | USA | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | USA | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | USA | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0022 | REF | REF | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0004 | REF | REF | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:99450355
|
T | C | 2 | a0001c0001a0001c0003 | 197 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(194): Show |
synonymous_variant | LOW | c.387T>C | p.Arg129Arg | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 4/8 | 527/1823 | 387/810 | 129/269 | chr7 | 99450355 | ||
chr7:99450781
|
G | A | 1 | a0001c0004 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.483G>A | p.Ser161Ser | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/8 | 623/1823 | 483/810 | 161/269 | chr7 | 99450781 | ||
chr7:99452416
|
G | A | 1 | a0001c0003 | 31 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(28): Show |
synonymous_variant | LOW | c.546G>A | p.Pro182Pro | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/8 | 686/1823 | 546/810 | 182/269 | chr7 | 99452416 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:99439026
|
C | G | 2 | a0001c0001t0003a0001c0001t0007 | 97 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(94): Show |
5_prime_UTR_variant | MODIFIER | c.-57C>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/8 | 57 | chr7 | 99439026 | |||||
chr7:99456538
|
C | T | 1 | a0001c0002t0013 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*38C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 38 | chr7 | 99456538 | |||||
chr7:99456640
|
G | A | 1 | a0001c0002t0008 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*140G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 140 | chr7 | 99456640 | |||||
chr7:99456666
|
T | G | 8 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(5): Show | 199 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*166T>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 166 | chr7 | 99456666 | |||||
chr7:99456737
|
G | A | 2 | a0001c0001t0004a0001c0003t0009 | 6 | HG01175.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*237G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 237 | chr7 | 99456737 | |||||
chr7:99456750
|
T | A | 2 | a0001c0002t0005a0001c0002t0011 | 4 | HG02165.hp2 NA18943.hp2 NA18982.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*250T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 250 | chr7 | 99456750 | |||||
chr7:99456751
|
G | A | 1 | a0001c0001t0007 | 3 | HG01884.hp2 HG02559.hp1 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*251G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 251 | chr7 | 99456751 | |||||
chr7:99456752
|
G | A | 2 | a0001c0002t0005a0001c0002t0011 | 4 | HG02165.hp2 NA18943.hp2 NA18982.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*252G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 252 | chr7 | 99456752 | |||||
chr7:99456782
|
G | A | 1 | a0001c0001t0004 | 5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*282G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 282 | chr7 | 99456782 | |||||
chr7:99456848
|
T | C | 1 | a0001c0001t0010 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*348T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 348 | chr7 | 99456848 | |||||
chr7:99456869
|
C | T | 1 | a0001c0003t0012 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*369C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 369 | chr7 | 99456869 | |||||
chr7:99457040
|
A | T | 1 | a0001c0002t0006 | 3 | HG00733.hp2 HG01358.hp2 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*540A>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 540 | chr7 | 99457040 | |||||
chr7:99457137
|
C | T | 1 | a0001c0002t0011 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*637C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 637 | chr7 | 99457137 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:99439297
|
G | A | 56 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0010others(53): Show | 61 | HG00323.hp1 HG00639.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.103+112G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99439297 | ||||||
chr7:99439355
|
C | T | 5 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+170C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99439355 | ||||||
chr7:99440204
|
C | T | 1 | a0001c0003t0002g0307 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.103+1019C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440204 | ||||||
chr7:99440360
|
T | C | 3 | a0001c0003t0002g0082a0001c0003t0002g0083a0001c0003t0002g0084 | 3 | HG02615.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.103+1175T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440360 | ||||||
chr7:99440378
|
G | T | 1 | a0001c0002t0001g0306 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.103+1193G>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440378 | ||||||
chr7:99440417
|
T | C | 1 | a0001c0002t0001g0085 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.103+1232T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440417 | ||||||
chr7:99440434
|
G | A | 30 | a0001c0003t0002g0082a0001c0003t0002g0083a0001c0003t0002g0084others(27): Show | 30 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.103+1249G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440434 | ||||||
chr7:99440458
|
C | T | 5 | a0001c0001t0002g0077a0001c0001t0002g0078a0001c0001t0002g0079others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+1273C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440458 | ||||||
chr7:99440557
|
T | G | 1 | a0001c0001t0002g0077 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.103+1372T>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440557 | ||||||
chr7:99440632
|
T | C | 35 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(32): Show | 35 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.103+1447T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440632 | ||||||
chr7:99440651
|
CTGGCATA others(16): Show |
C | 3 | a0001c0002t0002g0112a0001c0002t0002g0113a0001c0002t0002g0114 | 3 | HG02451.hp1 HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.103+1468_103+1490d others(25): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440651 | |||||
chr7:99440653
|
G | GGC | 6 | a0001c0003t0002g0098a0001c0003t0002g0099a0001c0003t0002g0102others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+1469_103+1470d others(4): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440653 | |||||
chr7:99440655
|
C | CAT | 7 | a0001c0002t0001g0006a0001c0002t0001g0021a0001c0002t0001g0195others(4): Show | 10 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.103+1489_103+1490d others(4): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440655 | |||||
chr7:99440655
|
C | CATATATA others(1): Show |
3 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0003t0002g0096 | 3 | HG02451.hp2 HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.103+1483_103+1490d others(10): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440655 | |||||
chr7:99440655
|
C | CATATATA others(3): Show |
2 | a0001c0001t0003g0127a0001c0001t0003g0128 | 2 | HG00621.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.103+1481_103+1490d others(12): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440655 | |||||
chr7:99440655
|
C | CATATATA others(5): Show |
1 | a0001c0001t0003g0121 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.103+1479_103+1490d others(14): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440655 | |||||
chr7:99440655
|
C | CATATATA others(13): Show |
1 | a0001c0003t0002g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.103+1471_103+1490d others(22): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440655 | |||||
chr7:99440655
|
C | CATATATA others(17): Show |
1 | a0001c0003t0002g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(26): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440655 | |||||
chr7:99440655
|
C | CATATATA others(21): Show |
3 | a0001c0001t0002g0116a0001c0003t0002g0088a0001c0003t0002g0089 | 3 | HG02809.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(30): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440655 | |||||
chr7:99440655
|
C | CGCATATA others(7): Show |
1 | a0001c0003t0002g0111 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.103+1470_103+1471i others(16): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440655 | ||||||
chr7:99440655
|
C | CGCATATA others(9): Show |
3 | a0001c0003t0002g0107a0001c0003t0002g0109a0001c0003t0009g0108 | 3 | HG01175.hp2 NA18939.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.103+1470_103+1471i others(18): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440655 | ||||||
chr7:99440655
|
C | CGCATATA others(11): Show |
3 | a0001c0003t0002g0104a0001c0003t0002g0105a0001c0003t0002g0307 | 3 | HG02523.hp2 NA18971.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.103+1470_103+1471i others(20): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440655 | ||||||
chr7:99440655
|
C | CGCATATA others(15): Show |
1 | a0001c0003t0002g0100 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.103+1470_103+1471i others(24): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440655 | ||||||
chr7:99440655
|
C | CGCATATA others(17): Show |
1 | a0001c0003t0002g0101 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.103+1470_103+1471i others(26): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440655 | ||||||
chr7:99440655
|
CATATATA others(1): Show |
C | 4 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311others(1): Show | 4 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+1483_103+1490d others(10): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440655 | |||||
chr7:99440656
|
A | G | 3 | a0001c0003t0002g0082a0001c0003t0002g0083a0001c0003t0002g0084 | 3 | HG02615.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.103+1471A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440656 | ||||||
chr7:99440657
|
T | C | 3 | a0001c0003t0002g0082a0001c0003t0002g0083a0001c0003t0002g0084 | 3 | HG02615.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.103+1472T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440657 | ||||||
chr7:99440663
|
T | C | 1 | a0001c0001t0003g0115 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.103+1478T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440663 | ||||||
chr7:99440666
|
ATATATAT others(3): Show |
A | 1 | a0001c0003t0002g0097 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.103+1483_103+1492d others(12): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440666 | |||||
chr7:99440666
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0002g0076 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.103+1483_103+1493d others(13): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440666 | |||||
chr7:99440672
|
A | T | 1 | a0001c0002t0011g0305 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.103+1487A>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440672 | ||||||
chr7:99440673
|
TA | T | 2 | a0001c0002t0001g0299a0001c0002t0005g0028 | 3 | NA18946.hp1 NA18982.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.103+1489delA | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440673 | ||||||
chr7:99440674
|
A | ATATATAT others(18): Show |
1 | a0001c0003t0002g0091 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(27): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(56): Show |
1 | a0001c0001t0002g0030 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(65): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(47): Show |
1 | a0001c0001t0002g0031 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(56): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(45): Show |
2 | a0001c0001t0002g0032a0001c0001t0002g0033 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(54): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(43): Show |
1 | a0001c0001t0002g0034 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(52): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(38): Show |
1 | a0001c0001t0002g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(47): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(36): Show |
1 | a0001c0001t0002g0036 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(45): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(30): Show |
1 | a0001c0003t0002g0086 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(39): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(34): Show |
1 | a0001c0001t0002g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(43): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0002g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(41): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(33): Show |
2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | HG03654.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(42): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(30): Show |
1 | a0001c0003t0002g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(39): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(30): Show |
2 | a0001c0001t0002g0041a0001c0001t0002g0042 | 2 | HG02257.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(39): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(31): Show |
2 | a0001c0001t0002g0043a0001c0001t0002g0044 | 2 | HG02083.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(40): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0002g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(41): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(22): Show |
1 | a0001c0003t0002g0099 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(31): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0002g0117 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(36): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(28): Show |
2 | a0001c0001t0002g0045a0001c0001t0002g0079 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(37): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(29): Show |
3 | a0001c0001t0002g0077a0001c0001t0002g0080a0001c0001t0002g0081 | 3 | HG02109.hp1 HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(38): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(21): Show |
1 | a0001c0003t0002g0102 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(30): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(26): Show |
2 | a0001c0001t0002g0118a0001c0003t0002g0103 | 2 | HG02486.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(35): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0002g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(34): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(27): Show |
11 | a0001c0001t0002g0009a0001c0001t0002g0046a0001c0001t0002g0048others(8): Show | 12 | HG00323.hp1 HG00639.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(36): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0002g0010 | 2 | HG02145.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(37): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(24): Show |
2 | a0001c0001t0002g0057a0001c0001t0002g0058 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(33): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(18): Show |
1 | a0001c0003t0002g0093 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(27): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(22): Show |
1 | a0001c0003t0002g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(31): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0003g0119 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(26): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(21): Show |
1 | a0001c0003t0002g0110 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(30): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0002g0059 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(29): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(13): Show |
1 | a0001c0003t0002g0094 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(22): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0003g0120 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(23): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0002g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(28): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0003g0122 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(23): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0003g0123a0001c0001t0003g0124 | 2 | NA18947.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(24): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(16): Show |
2 | a0001c0001t0003g0012a0001c0001t0003g0125 | 3 | NA18948.hp2 NA18966.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(25): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0007g0129 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(19): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0003g0130 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(21): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0003g0131a0001c0001t0003g0132 | 2 | NA18982.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(22): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0003g0133a0001c0001t0003g0134 | 2 | HG04184.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(23): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(15): Show |
4 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0003g0137others(1): Show | 4 | HG01496.hp2 HG02071.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(24): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0003g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(25): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(15): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0003g0141a0001c0001t0007g0140 | 2 | HG02818.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(19): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(11): Show |
2 | a0001c0001t0003g0143a0001c0001t0007g0142 | 2 | HG02559.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(20): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(12): Show |
5 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(2): Show | 5 | NA18944.hp2 NA18980.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(21): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(13): Show |
12 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(9): Show | 15 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(12): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(22): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(14): Show |
9 | a0001c0001t0003g0016a0001c0001t0003g0158a0001c0001t0003g0159others(6): Show | 10 | HG02735.hp1 HG02735.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(23): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(15): Show |
4 | a0001c0001t0003g0166a0001c0001t0003g0167a0001c0001t0003g0168others(1): Show | 4 | HG02074.hp2 HG02523.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(24): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0003g0170 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(25): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0003g0171 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(27): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0003g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(15): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0003g0173 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(18): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(10): Show |
3 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0003g0176 | 3 | HG03942.hp2 NA18963.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(19): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(11): Show |
2 | a0001c0001t0003g0177a0001c0001t0003g0178 | 2 | HG02602.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(20): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(12): Show |
5 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0003g0181others(2): Show | 5 | HG00280.hp2 HG02622.hp1 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(21): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(13): Show |
6 | a0001c0001t0003g0017a0001c0001t0003g0184a0001c0001t0003g0185others(3): Show | 7 | HG01099.hp2 HG02132.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(22): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(14): Show |
3 | a0001c0001t0003g0189a0001c0001t0003g0190a0001c0001t0003g0191 | 3 | NA18956.hp1 NA18969.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(23): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0003g0192 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(24): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0003g0193 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(25): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(11): Show |
3 | a0001c0001t0003g0196a0001c0001t0003g0197a0001c0001t0003g0198 | 3 | HG00544.hp1 HG02109.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(20): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(12): Show |
5 | a0001c0001t0003g0115a0001c0001t0003g0199a0001c0001t0003g0200others(2): Show | 5 | HG00438.hp1 HG03516.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(21): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0003g0203 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(23): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATTT others(3): Show |
3 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067 | 3 | HG01081.hp1 HG01167.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(12): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | ATATATTT others(13): Show |
1 | a0001c0001t0003g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(22): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440674
|
A | T | 7 | a0001c0002t0001g0029a0001c0002t0001g0302a0001c0002t0001g0303others(4): Show | 8 | HG01109.hp2 HG02165.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.103+1489A>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440674 | ||||||
chr7:99440674
|
AT | A | 25 | a0001c0002t0001g0018a0001c0002t0001g0022a0001c0002t0001g0204others(22): Show | 27 | HG00323.hp2 HG00735.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.103+1508delT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | |||||
chr7:99440675
|
T | TA | 22 | a0001c0002t0001g0007a0001c0002t0001g0194a0001c0002t0001g0213others(19): Show | 24 | HG00099.hp2 HG00544.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(3): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440675 | ||||||
chr7:99440675
|
T | TATATATA others(2): Show |
3 | a0001c0001t0002g0063a0001c0001t0003g0126a0001c0003t0002g0095 | 3 | HG01081.hp2 HG03453.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(11): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440675 | ||||||
chr7:99440675
|
T | TATATATA others(20): Show |
1 | a0001c0003t0002g0087 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(29): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440675 | ||||||
chr7:99440676
|
T | A | 63 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0003g0121others(60): Show | 80 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.103+1491T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440676 | ||||||
chr7:99440676
|
T | G | 1 | a0001c0001t0002g0046 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.103+1491T>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440676 | ||||||
chr7:99440677
|
T | A | 36 | a0001c0001t0003g0126a0001c0002t0001g0007a0001c0002t0001g0018others(33): Show | 39 | HG00544.hp2 HG00735.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.103+1492T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440677 | ||||||
chr7:99440678
|
T | A | 14 | a0001c0002t0001g0006a0001c0002t0001g0195a0001c0002t0001g0206others(11): Show | 16 | HG00597.hp2 HG01123.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.103+1493T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440678 | ||||||
chr7:99440679
|
T | A | 4 | a0001c0002t0001g0194a0001c0002t0001g0204a0001c0002t0001g0205others(1): Show | 4 | HG01081.hp2 HG01952.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+1494T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440679 | ||||||
chr7:99440680
|
T | A | 1 | a0001c0003t0002g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.103+1495T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440680 | ||||||
chr7:99440682
|
T | G | 3 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033 | 3 | HG02965.hp1 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.103+1497T>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440682 | ||||||
chr7:99440693
|
T | C | 1 | a0001c0003t0002g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.103+1508T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440693 | ||||||
chr7:99440706
|
A | ACAACTTT others(18): Show |
1 | a0001c0002t0001g0298 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.103+1522_103+1546d others(27): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440706 | |||||
chr7:99440837
|
C | T | 5 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+1652C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440837 | ||||||
chr7:99440947
|
C | CT | 18 | a0001c0001t0003g0202a0001c0001t0004g0308a0001c0001t0004g0309others(15): Show | 18 | HG01081.hp2 HG01169.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.103+1782dupT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440947 | |||||
chr7:99440947
|
CT | C | 17 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0048others(14): Show | 20 | HG00639.hp2 HG01069.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.103+1782delT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440947 | |||||
chr7:99441051
|
A | G | 4 | a0001c0002t0001g0264a0001c0002t0001g0265a0001c0002t0001g0266others(1): Show | 4 | HG00408.hp2 HG01934.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+1866A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441051 | ||||||
chr7:99441107
|
C | A | 1 | a0001c0001t0007g0140 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.103+1922C>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441107 | ||||||
chr7:99441281
|
GA | G | 3 | a0001c0003t0002g0091a0001c0003t0002g0095a0001c0003t0002g0096 | 3 | HG01081.hp2 HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.103+2097delA | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441281 | ||||||
chr7:99441283
|
G | T | 3 | a0001c0003t0002g0091a0001c0003t0002g0095a0001c0003t0002g0096 | 3 | HG01081.hp2 HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.103+2098G>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441283 | ||||||
chr7:99441293
|
C | T | 2 | a0001c0001t0004g0311a0001c0001t0004g0312 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.103+2108C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441293 | ||||||
chr7:99441389
|
C | T | 1 | a0001c0002t0001g0263 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.103+2204C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441389 | ||||||
chr7:99441690
|
A | AT | 57 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0010others(54): Show | 62 | HG00323.hp1 HG00639.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.103+2515dupT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99441690 | |||||
chr7:99441690
|
A | G | 1 | a0001c0002t0001g0270 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.103+2505A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441690 | ||||||
chr7:99441703
|
T | C | 1 | a0001c0002t0001g0207 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.103+2518T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441703 | ||||||
chr7:99441827
|
G | A | 30 | a0001c0003t0002g0082a0001c0003t0002g0083a0001c0003t0002g0084others(27): Show | 30 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.103+2642G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441827 | ||||||
chr7:99441981
|
C | T | 30 | a0001c0003t0002g0082a0001c0003t0002g0083a0001c0003t0002g0084others(27): Show | 30 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.103+2796C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441981 | ||||||
chr7:99442004
|
T | C | 30 | a0001c0003t0002g0082a0001c0003t0002g0083a0001c0003t0002g0084others(27): Show | 30 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.104-2785T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442004 | ||||||
chr7:99442220
|
A | G | 3 | a0001c0003t0002g0087a0001c0003t0002g0088a0001c0003t0002g0089 | 3 | HG02970.hp1 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.104-2569A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442220 | ||||||
chr7:99442411
|
C | T | 2 | a0001c0001t0004g0309a0001c0001t0004g0310 | 2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.104-2378C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442411 | ||||||
chr7:99442453
|
G | A | 1 | a0001c0003t0002g0097 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.104-2336G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442453 | ||||||
chr7:99442453
|
G | C | 1 | a0001c0002t0001g0264 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.104-2336G>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442453 | ||||||
chr7:99442642
|
C | T | 1 | a0001c0001t0003g0176 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.104-2147C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442642 | ||||||
chr7:99442650
|
C | T | 88 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(85): Show | 94 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.104-2139C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442650 | ||||||
chr7:99442651
|
G | A | 1 | a0001c0002t0001g0229 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.104-2138G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442651 | ||||||
chr7:99442655
|
C | CA | 36 | a0001c0002t0001g0023a0001c0002t0001g0214a0001c0002t0001g0215others(33): Show | 37 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.104-2114dupA | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99442655 | |||||
chr7:99442655
|
C | CAA | 31 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0063others(28): Show | 31 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.104-2115_104-2114d others(4): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99442655 | |||||
chr7:99442655
|
C | CAAA | 51 | a0001c0001t0002g0046a0001c0001t0002g0058a0001c0001t0002g0069others(48): Show | 55 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.104-2116_104-2114d others(5): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99442655 | |||||
chr7:99442655
|
C | CAAAA | 58 | a0001c0001t0002g0009a0001c0001t0002g0030a0001c0001t0002g0031others(55): Show | 60 | HG00639.hp1 HG01070.hp1 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.104-2117_104-2114d others(6): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99442655 | |||||
chr7:99442655
|
C | CAAAAA | 15 | a0001c0001t0002g0010a0001c0001t0002g0032a0001c0001t0002g0036others(12): Show | 17 | HG00408.hp1 HG00597.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.104-2118_104-2114d others(7): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99442655 | |||||
chr7:99442669
|
A | AAC | 3 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0064 | 6 | HG01884.hp1 HG02922.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-2119_104-2118i others(4): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99442669 | |||||
chr7:99442669
|
A | AC | 5 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-2120_104-2119i others(3): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442669 | ||||||
chr7:99442669
|
A | C | 1 | a0001c0002t0001g0261 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.104-2120A>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442669 | ||||||
chr7:99442676
|
C | A | 9 | a0001c0001t0003g0139a0001c0001t0003g0149a0001c0001t0003g0159others(6): Show | 9 | HG01978.hp2 HG02293.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.104-2113C>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442676 | ||||||
chr7:99442749
|
C | T | 1 | a0001c0001t0003g0154 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.104-2040C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442749 | ||||||
chr7:99442837
|
G | A | 1 | a0001c0001t0004g0311 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.104-1952G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442837 | ||||||
chr7:99442899
|
C | T | 1 | a0001c0001t0007g0129 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.104-1890C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442899 | ||||||
chr7:99443343
|
T | A | 2 | a0001c0001t0002g0039a0001c0001t0002g0060 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.104-1446T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99443343 | ||||||
chr7:99443433
|
G | GC | 36 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(33): Show | 36 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.104-1356_104-1355i others(3): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99443433 | ||||||
chr7:99443495
|
A | T | 1 | a0001c0001t0003g0176 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.104-1294A>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99443495 | ||||||
chr7:99443610
|
G | A | 2 | a0001c0003t0002g0106a0001c0003t0002g0110 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.104-1179G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99443610 | ||||||
chr7:99443748
|
A | G | 1 | a0001c0002t0001g0217 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.104-1041A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99443748 | ||||||
chr7:99443788
|
G | T | 3 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0118 | 3 | HG02647.hp1 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.104-1001G>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99443788 | ||||||
chr7:99443793
|
C | A | 10 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0104others(7): Show | 10 | HG00099.hp2 HG01175.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.104-996C>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99443793 | ||||||
chr7:99443854
|
G | A | 1 | a0001c0002t0001g0289 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.104-935G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99443854 | ||||||
chr7:99443975
|
G | C | 31 | a0001c0003t0002g0082a0001c0003t0002g0083a0001c0003t0002g0084others(28): Show | 31 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.104-814G>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99443975 | ||||||
chr7:99444297
|
A | T | 1 | a0001c0003t0002g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.104-492A>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99444297 | ||||||
chr7:99444401
|
G | A | 89 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(86): Show | 95 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.104-388G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99444401 | ||||||
chr7:99444419
|
T | C | 25 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0194others(22): Show | 27 | HG00099.hp1 HG00733.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.104-370T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99444419 | ||||||
chr7:99444457
|
C | CA | 7 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(4): Show | 8 | HG00738.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104-319dupA | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99444457 | |||||
chr7:99444487
|
G | A | 2 | a0001c0001t0003g0136a0001c0001t0003g0163 | 2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.104-302G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99444487 | ||||||
chr7:99444550
|
C | A | 2 | a0001c0002t0001g0287a0001c0002t0001g0292 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.104-239C>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99444550 | ||||||
chr7:99444579
|
C | T | 1 | a0001c0001t0003g0156 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.104-210C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99444579 | ||||||
chr7:99444872
|
G | A | 1 | a0001c0001t0003g0137 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.154+33G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99444872 | ||||||
chr7:99444879
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.154+40C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99444879 | ||||||
chr7:99445022
|
C | G | 2 | a0001c0001t0004g0309a0001c0001t0004g0310 | 2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.154+183C>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445022 | ||||||
chr7:99445071
|
G | A | 14 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0064others(11): Show | 17 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.154+232G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445071 | ||||||
chr7:99445241
|
C | A | 1 | a0001c0002t0001g0213 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.154+402C>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445241 | ||||||
chr7:99445276
|
T | A | 1 | a0001c0001t0003g0187 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.154+437T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445276 | ||||||
chr7:99445277
|
C | A | 1 | a0001c0001t0003g0187 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.154+438C>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445277 | ||||||
chr7:99445298
|
G | A | 1 | a0001c0003t0002g0097 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.154+459G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445298 | ||||||
chr7:99445321
|
C | T | 1 | a0001c0001t0003g0189 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.154+482C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445321 | ||||||
chr7:99445372
|
C | T | 1 | a0001c0001t0003g0165 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.154+533C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445372 | ||||||
chr7:99445412
|
C | CA | 12 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(9): Show | 12 | HG00558.hp1 HG01081.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.154+587dupA | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99445412 | |||||
chr7:99445544
|
C | T | 1 | a0001c0002t0001g0019 | 2 | HG00099.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.154+705C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445544 | ||||||
chr7:99445756
|
C | T | 1 | a0001c0003t0002g0093 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.154+917C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445756 | ||||||
chr7:99445823
|
G | A | 3 | a0001c0002t0002g0112a0001c0002t0002g0113a0001c0002t0002g0114 | 3 | HG02451.hp1 HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.154+984G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445823 | ||||||
chr7:99446041
|
G | A | 1 | a0001c0003t0002g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.154+1202G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99446041 | ||||||
chr7:99446230
|
C | A | 4 | a0001c0002t0001g0213a0001c0002t0001g0218a0001c0002t0001g0219others(1): Show | 4 | NA18983.hp1 NA19058.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+1391C>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99446230 | ||||||
chr7:99446347
|
A | T | 4 | a0001c0001t0003g0173a0001c0001t0003g0174a0001c0001t0003g0175others(1): Show | 4 | HG00544.hp1 NA18963.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+1508A>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99446347 | ||||||
chr7:99446604
|
CT | C | 17 | a0001c0001t0002g0046a0001c0001t0002g0053a0001c0001t0002g0057others(14): Show | 17 | HG00323.hp1 HG01074.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.155-1502delT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446604 | |||||
chr7:99446619
|
TA | T | 19 | a0001c0001t0003g0015a0001c0001t0003g0120a0001c0001t0003g0121others(16): Show | 20 | HG00621.hp2 HG02040.hp2 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.155-1496delA | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446619 | |||||
chr7:99446620
|
A | T | 106 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0118others(103): Show | 111 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.155-1501A>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99446620 | ||||||
chr7:99446621
|
A | T | 1 | a0001c0001t0003g0126 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.155-1500A>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99446621 | ||||||
chr7:99446699
|
C | CT | 3 | a0001c0003t0002g0082a0001c0003t0002g0083a0001c0003t0002g0084 | 3 | HG02615.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.155-1421dupT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446699 | |||||
chr7:99446771
|
C | CT | 78 | a0001c0001t0002g0040a0001c0001t0002g0042a0001c0001t0002g0046others(75): Show | 94 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.155-1313dupT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446771
|
C | CTT | 43 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0034others(40): Show | 53 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.155-1314_155-1313d others(4): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446771
|
C | CTTT | 23 | a0001c0001t0002g0011a0001c0001t0002g0030a0001c0001t0002g0033others(20): Show | 24 | HG01081.hp1 HG01167.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.155-1315_155-1313d others(5): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446771
|
C | CTTTT | 15 | a0001c0001t0002g0005a0001c0001t0002g0031a0001c0001t0002g0032others(12): Show | 18 | HG00438.hp1 HG01069.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.155-1316_155-1313d others(6): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446771
|
C | CTTTTT | 6 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0067others(3): Show | 6 | HG01517.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.155-1317_155-1313d others(7): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446771
|
C | CTTTTTTT others(1): Show |
6 | a0001c0001t0002g0044a0001c0001t0007g0140a0001c0002t0002g0112others(3): Show | 6 | HG02083.hp1 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.155-1320_155-1313d others(10): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446771
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0002g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.155-1322_155-1313d others(12): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446771
|
C | CTTTTTTT others(4): Show |
2 | a0001c0003t0002g0101a0001c0003t0002g0307 | 2 | HG00099.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.155-1323_155-1313d others(13): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446771
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0002g0069 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.155-1324_155-1313d others(14): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446771
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0002g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.155-1325_155-1313d others(15): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446771
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0010g0075 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.155-1326_155-1313d others(16): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446771
|
C | CTTTTTTT others(11): Show |
2 | a0001c0003t0002g0082a0001c0003t0002g0083 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.155-1330_155-1313d others(20): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446771
|
C | CTTTTTTT others(18): Show |
1 | a0001c0003t0002g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.155-1337_155-1313d others(27): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446771
|
C | CTTTTTTT others(20): Show |
1 | a0001c0003t0002g0111 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.155-1339_155-1313d others(29): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446771
|
CT | C | 24 | a0001c0001t0002g0057a0001c0001t0003g0012a0001c0001t0003g0015others(21): Show | 27 | HG00280.hp2 HG01070.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.155-1313delT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446771
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0003t0009g0108 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.155-1325_155-1313d others(15): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446771
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0002t0001g0277 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.155-1327_155-1313d others(17): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446771
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0002t0001g0215 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.155-1329_155-1313d others(19): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446771
|
CTTTTTTT others(11): Show |
C | 2 | a0001c0002t0001g0019a0001c0002t0001g0247 | 3 | HG00099.hp1 HG00735.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.155-1330_155-1313d others(20): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446771
|
CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0002g0070 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.155-1333_155-1313d others(23): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | |||||
chr7:99446774
|
T | C | 1 | a0001c0001t0003g0152 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.155-1347T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99446774 | ||||||
chr7:99446809
|
A | G | 189 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0010others(186): Show | 200 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.155-1312A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99446809 | ||||||
chr7:99446880
|
C | T | 2 | a0001c0002t0001g0024a0001c0002t0001g0291 | 3 | HG00738.hp1 HG04228.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.155-1241C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99446880 | ||||||
chr7:99447042
|
T | C | 36 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(33): Show | 36 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.155-1079T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447042 | ||||||
chr7:99447056
|
A | G | 36 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(33): Show | 36 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.155-1065A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447056 | ||||||
chr7:99447109
|
G | GCTTA | 189 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0010others(186): Show | 200 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.155-995_155-992dup others(4): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99447109 | |||||
chr7:99447255
|
CTTTCTTT others(5): Show |
C | 48 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0061others(45): Show | 51 | HG00099.hp2 HG01081.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.155-850_155-839del others(12): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99447255 | |||||
chr7:99447259
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.155-850_155-838del others(13): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99447259 | |||||
chr7:99447263
|
T | A | 1 | a0001c0002t0001g0268 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.155-858T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447263 | ||||||
chr7:99447283
|
T | C | 1 | a0001c0002t0001g0221 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.155-838T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447283 | ||||||
chr7:99447291
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.155-830A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447291 | ||||||
chr7:99447339
|
G | A | 3 | a0001c0002t0001g0025a0001c0002t0001g0289a0001c0002t0001g0293 | 4 | HG00423.hp2 HG02074.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-782G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447339 | ||||||
chr7:99447350
|
C | A | 5 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-771C>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447350 | ||||||
chr7:99447541
|
C | T | 1 | a0001c0003t0002g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.155-580C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447541 | ||||||
chr7:99447589
|
C | CT | 99 | a0001c0001t0002g0069a0001c0001t0002g0071a0001c0001t0002g0074others(96): Show | 105 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.155-514dupT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99447589 | |||||
chr7:99447589
|
CT | C | 40 | a0001c0001t0002g0054a0001c0002t0001g0208a0001c0002t0001g0214others(37): Show | 40 | HG00099.hp2 HG00544.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.155-514delT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99447589 | |||||
chr7:99447676
|
G | A | 11 | a0001c0003t0002g0093a0001c0003t0002g0100a0001c0003t0002g0101others(8): Show | 11 | HG00099.hp2 HG01175.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-445G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447676 | ||||||
chr7:99447691
|
G | C | 1 | a0001c0001t0002g0040 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.155-430G>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447691 | ||||||
chr7:99447794
|
A | C | 1 | a0001c0002t0001g0257 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.155-327A>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447794 | ||||||
chr7:99447841
|
A | C | 4 | a0001c0003t0002g0086a0001c0003t0002g0091a0001c0003t0002g0095others(1): Show | 4 | HG01081.hp2 HG01891.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-280A>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447841 | ||||||
chr7:99447979
|
G | A | 1 | a0001c0001t0003g0134 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.155-142G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447979 | ||||||
chr7:99448406
|
C | T | 1 | a0001c0003t0002g0097 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.307+133C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99448406 | ||||||
chr7:99448459
|
C | CT | 13 | a0001c0001t0002g0069a0001c0001t0002g0071a0001c0001t0002g0074others(10): Show | 13 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.307+207dupT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 99448459 | |||||
chr7:99448459
|
CT | C | 42 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0045others(39): Show | 44 | HG00323.hp2 HG00639.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.307+207delT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 99448459 | |||||
chr7:99448591
|
C | T | 3 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0118 | 3 | HG02647.hp1 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.307+318C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99448591 | ||||||
chr7:99448621
|
T | C | 3 | a0001c0002t0001g0211a0001c0002t0001g0234a0001c0002t0001g0276 | 3 | HG02165.hp1 NA18961.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.307+348T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99448621 | ||||||
chr7:99448627
|
G | A | 3 | a0001c0002t0001g0211a0001c0002t0001g0234a0001c0002t0001g0276 | 3 | HG02165.hp1 NA18961.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.307+354G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99448627 | ||||||
chr7:99448643
|
A | G | 3 | a0001c0003t0002g0087a0001c0003t0002g0088a0001c0003t0002g0089 | 3 | HG02970.hp1 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.307+370A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99448643 | ||||||
chr7:99448849
|
A | C | 5 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.307+576A>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99448849 | ||||||
chr7:99448850
|
G | T | 5 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.307+577G>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99448850 | ||||||
chr7:99448981
|
G | A | 5 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0071others(2): Show | 5 | HG02559.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.307+708G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99448981 | ||||||
chr7:99448994
|
G | A | 38 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0030others(35): Show | 40 | HG00323.hp1 HG00639.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.307+721G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99448994 | ||||||
chr7:99449071
|
G | A | 1 | a0001c0002t0001g0293 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.307+798G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449071 | ||||||
chr7:99449078
|
A | G | 1 | a0001c0002t0001g0247 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.307+805A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449078 | ||||||
chr7:99449093
|
C | G | 1 | a0001c0001t0002g0042 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.307+820C>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449093 | ||||||
chr7:99449407
|
T | A | 31 | a0001c0003t0002g0082a0001c0003t0002g0083a0001c0003t0002g0084others(28): Show | 31 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.308-869T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449407 | ||||||
chr7:99449476
|
G | A | 3 | a0001c0001t0007g0129a0001c0001t0007g0140a0001c0001t0007g0142 | 3 | HG01884.hp2 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.308-800G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449476 | ||||||
chr7:99449486
|
T | G | 2 | a0001c0001t0004g0311a0001c0001t0004g0312 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.308-790T>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449486 | ||||||
chr7:99449567
|
C | T | 4 | a0001c0002t0001g0232a0001c0002t0001g0245a0001c0002t0001g0246others(1): Show | 4 | HG01070.hp2 HG01167.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.308-709C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449567 | ||||||
chr7:99449569
|
T | C | 1 | a0001c0002t0001g0255 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.308-707T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449569 | ||||||
chr7:99449749
|
T | G | 2 | a0001c0002t0001g0294a0001c0002t0001g0302 | 2 | NA18942.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.308-527T>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449749 | ||||||
chr7:99449842
|
G | T | 2 | a0001c0001t0003g0155a0001c0001t0003g0188 | 2 | HG00558.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.308-434G>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449842 | ||||||
chr7:99449859
|
G | C | 3 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0118 | 3 | HG02647.hp1 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.308-417G>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449859 | ||||||
chr7:99450170
|
G | A | 1 | a0001c0002t0001g0258 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.308-106G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99450170 | ||||||
chr7:99450174
|
G | A | 1 | a0001c0002t0001g0275 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.308-102G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99450174 | ||||||
chr7:99450190
|
A | G | 3 | a0001c0001t0007g0129a0001c0001t0007g0140a0001c0001t0007g0142 | 3 | HG01884.hp2 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.308-86A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99450190 | ||||||
chr7:99450398
|
G | A | 3 | a0001c0001t0007g0129a0001c0001t0007g0140a0001c0001t0007g0142 | 3 | HG01884.hp2 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.403+27G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 4/7 | chr7 | 99450398 | ||||||
chr7:99450509
|
C | T | 4 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0063others(1): Show | 4 | HG02451.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+138C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 4/7 | chr7 | 99450509 | ||||||
chr7:99450520
|
C | A | 36 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(33): Show | 36 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.403+149C>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 4/7 | chr7 | 99450520 | ||||||
chr7:99450603
|
C | T | 4 | a0001c0003t0002g0086a0001c0003t0002g0091a0001c0003t0002g0095others(1): Show | 4 | HG01081.hp2 HG01891.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-99C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 4/7 | chr7 | 99450603 | ||||||
chr7:99450680
|
G | A | 3 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0118 | 3 | HG02647.hp1 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.404-22G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 4/7 | chr7 | 99450680 | ||||||
chr7:99450809
|
T | C | 186 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0010others(183): Show | 197 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.497+14T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99450809 | ||||||
chr7:99450916
|
G | A | 5 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.497+121G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99450916 | ||||||
chr7:99450964
|
T | C | 1 | a0001c0003t0002g0307 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.497+169T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99450964 | ||||||
chr7:99451000
|
G | A | 3 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0118 | 3 | HG02647.hp1 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.497+205G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99451000 | ||||||
chr7:99451038
|
A | G | 3 | a0001c0002t0002g0112a0001c0002t0002g0113a0001c0002t0002g0114 | 3 | HG02451.hp1 HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.497+243A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99451038 | ||||||
chr7:99451475
|
C | T | 56 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0010others(53): Show | 61 | HG00323.hp1 HG00639.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.497+680C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99451475 | ||||||
chr7:99451541
|
G | C | 31 | a0001c0003t0002g0082a0001c0003t0002g0083a0001c0003t0002g0084others(28): Show | 31 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.497+746G>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99451541 | ||||||
chr7:99451566
|
C | T | 20 | a0001c0003t0002g0082a0001c0003t0002g0083a0001c0003t0002g0084others(17): Show | 20 | HG00099.hp2 HG01175.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.497+771C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99451566 | ||||||
chr7:99451691
|
G | A | 3 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0118 | 3 | HG02647.hp1 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.498-677G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99451691 | ||||||
chr7:99451766
|
G | A | 20 | a0001c0003t0002g0082a0001c0003t0002g0083a0001c0003t0002g0084others(17): Show | 20 | HG00099.hp2 HG01175.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.498-602G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99451766 | ||||||
chr7:99451780
|
A | G | 189 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0010others(186): Show | 200 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.498-588A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99451780 | ||||||
chr7:99451871
|
C | T | 6 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(3): Show | 6 | HG01243.hp2 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.498-497C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99451871 | ||||||
chr7:99452059
|
C | T | 14 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0064others(11): Show | 17 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.498-309C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99452059 | ||||||
chr7:99452167
|
G | A | 1 | a0001c0001t0003g0181 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.498-201G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99452167 | ||||||
chr7:99452190
|
G | A | 1 | a0001c0001t0004g0311 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.498-178G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99452190 | ||||||
chr7:99452253
|
C | T | 18 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0061others(15): Show | 21 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.498-115C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99452253 | ||||||
chr7:99452489
|
C | T | 1 | a0001c0002t0001g0296 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.570+49C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/7 | chr7 | 99452489 | ||||||
chr7:99452509
|
A | T | 1 | a0001c0001t0002g0070 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.570+69A>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/7 | chr7 | 99452509 | ||||||
chr7:99452700
|
G | A | 91 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(88): Show | 97 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.570+260G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/7 | chr7 | 99452700 | ||||||
chr7:99452759
|
C | T | 5 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+319C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/7 | chr7 | 99452759 | ||||||
chr7:99453323
|
G | A | 1 | a0001c0002t0001g0225 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.571-643G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/7 | chr7 | 99453323 | ||||||
chr7:99453364
|
G | A | 11 | a0001c0003t0002g0093a0001c0003t0002g0100a0001c0003t0002g0101others(8): Show | 11 | HG00099.hp2 HG01175.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.571-602G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/7 | chr7 | 99453364 | ||||||
chr7:99453414
|
C | T | 1 | a0001c0001t0002g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.571-552C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/7 | chr7 | 99453414 | ||||||
chr7:99453616
|
C | T | 1 | a0001c0001t0003g0166 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.571-350C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/7 | chr7 | 99453616 | ||||||
chr7:99453801
|
TCAC | T | 6 | a0001c0003t0002g0087a0001c0003t0002g0088a0001c0003t0002g0089others(3): Show | 6 | HG02258.hp1 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-161_571-159del others(3): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 99453801 | |||||
chr7:99454185
|
T | A | 1 | a0001c0001t0003g0187 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.741+49T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99454185 | ||||||
chr7:99454233
|
A | C | 18 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0061others(15): Show | 21 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.741+97A>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99454233 | ||||||
chr7:99454306
|
T | C | 1 | a0001c0001t0002g0077 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.741+170T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99454306 | ||||||
chr7:99454462
|
G | A | 4 | a0001c0001t0003g0193a0001c0002t0002g0112a0001c0002t0002g0113others(1): Show | 4 | HG02451.hp1 HG02615.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.741+326G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99454462 | ||||||
chr7:99454805
|
T | C | 129 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0118others(126): Show | 135 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.741+669T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99454805 | ||||||
chr7:99454927
|
C | T | 3 | a0001c0002t0002g0112a0001c0002t0002g0113a0001c0002t0002g0114 | 3 | HG02451.hp1 HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.741+791C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99454927 | ||||||
chr7:99454951
|
A | G | 1 | a0001c0002t0001g0263 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.741+815A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99454951 | ||||||
chr7:99455048
|
CTT | C | 5 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.741+914_741+915del others(2): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 99455048 | |||||
chr7:99455087
|
A | G | 30 | a0001c0003t0002g0082a0001c0003t0002g0083a0001c0003t0002g0084others(27): Show | 30 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.741+951A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455087 | ||||||
chr7:99455283
|
T | A | 1 | a0001c0001t0003g0187 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.741+1147T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455283 | ||||||
chr7:99455485
|
G | A | 2 | a0001c0002t0001g0242a0001c0002t0001g0258 | 2 | NA18965.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.742-947G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455485 | ||||||
chr7:99455552
|
T | C | 2 | a0001c0001t0002g0117a0001c0001t0002g0118 | 2 | HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.742-880T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455552 | ||||||
chr7:99455585
|
C | T | 1 | a0001c0001t0002g0056 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.742-847C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455585 | ||||||
chr7:99455678
|
G | A | 1 | a0001c0002t0001g0256 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.742-754G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455678 | ||||||
chr7:99455691
|
G | C | 38 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0030others(35): Show | 40 | HG00323.hp1 HG00639.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.742-741G>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455691 | ||||||
chr7:99455754
|
G | A | 18 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0061others(15): Show | 21 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.742-678G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455754 | ||||||
chr7:99455789
|
C | T | 1 | a0001c0002t0008g0230 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.742-643C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455789 | ||||||
chr7:99455841
|
C | G | 1 | a0001c0002t0001g0222 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.742-591C>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455841 | ||||||
chr7:99455876
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.742-556C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455876 | ||||||
chr7:99455948
|
A | G | 1 | a0001c0003t0002g0097 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.742-484A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455948 | ||||||
chr7:99456048
|
C | T | 5 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.742-384C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99456048 | ||||||
chr7:99456176
|
C | T | 5 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.742-256C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99456176 | ||||||
chr7:99456186
|
C | T | 2 | a0001c0003t0002g0090a0001c0003t0002g0092 | 2 | HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.742-246C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99456186 | ||||||
chr7:99456193
|
G | A | 14 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0040others(11): Show | 16 | HG00323.hp1 HG00639.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.742-239G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99456193 | ||||||
chr7:99456203
|
G | C | 1 | a0001c0002t0001g0236 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.742-229G>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99456203 | ||||||
chr7:99456210
|
C | T | 1 | a0001c0001t0003g0151 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.742-222C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99456210 | ||||||
chr7:99456211
|
G | A | 1 | a0001c0001t0002g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.742-221G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99456211 |