geneid | 53981 |
---|---|
ensemblid | ENSG00000165934.13 |
hgncid | 2325 |
symbol | CPSF2 |
name | cleavage and polyadenylation specific factor 2 |
refseq_nuc | NM_017437.3 |
refseq_prot | NP_059133.1 |
ensembl_nuc | ENST00000298875.9 |
ensembl_prot | ENSP00000298875.4 |
mane_status | MANE Select |
chr | chr14 |
start | 92121969 |
end | 92172145 |
strand | + |
ver | v1.2 |
region | chr14:92121969-92172145 |
region5000 | chr14:92116969-92177145 |
regionname0 | CPSF2_chr14_92121969_92172145 |
regionname5000 | CPSF2_chr14_92116969_92177145 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 782 | 387 | 86 | 60 | 183 | 12 | 44 | 145 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0002 | 0/0 | 782 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2349 | 386 | 86 | 60 | 182 | 12 | 44 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
c0002 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
c0003 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 10654 | 31 | 3 | 1 | 25 | 0 | 2 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0002 | 1/0 | 10655 | 26 | 6 | 10 | 0 | 3 | 6 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0003 | 0/0 | 10679 | 22 | 1 | 5 | 14 | 1 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0004 | 0/0 | 10678 | 18 | 2 | 1 | 14 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0005 | 0/0 | 10673 | 16 | 2 | 2 | 10 | 0 | 2 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0006 | 0/0 | 10674 | 11 | 3 | 1 | 7 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0007 | 0/0 | 10656 | 9 | 0 | 9 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0008 | 0/0 | 10655 | 8 | 2 | 0 | 5 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0009 | 0/0 | 10655 | 8 | 0 | 0 | 7 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0010 | 0/0 | 10680 | 8 | 0 | 3 | 4 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0011 | 0/0 | 10654 | 5 | 2 | 1 | 0 | 2 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0012 | 0/0 | 10672 | 5 | 0 | 0 | 5 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0013 | 0/0 | 10675 | 5 | 0 | 1 | 4 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0014 | 0/0 | 10662 | 4 | 3 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0015 | 0/0 | 10654 | 4 | 2 | 0 | 0 | 0 | 2 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0016 | 0/0 | 10671 | 4 | 2 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0017 | 0/0 | 10672 | 4 | 2 | 1 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0018 | 0/0 | 10680 | 4 | 0 | 0 | 4 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0019 | 0/0 | 10681 | 4 | 0 | 1 | 2 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0020 | 0/0 | 10661 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0021 | 0/0 | 10662 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0022 | 0/0 | 10650 | 3 | 1 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0023 | 0/0 | 10654 | 3 | 0 | 0 | 0 | 0 | 3 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0024 | 0/0 | 10655 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0025 | 0/0 | 10657 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0026 | 0/0 | 10655 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0027 | 0/0 | 10655 | 3 | 1 | 1 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0028 | 0/0 | 10656 | 3 | 1 | 1 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0029 | 0/0 | 10678 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0030 | 0/0 | 10655 | 2 | 0 | 1 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0031 | 0/0 | 10660 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0032 | 0/0 | 10660 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0033 | 0/0 | 10662 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0034 | 0/0 | 10683 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0035 | 0/0 | 10684 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0036 | 0/0 | 10689 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0037 | 0/0 | 10685 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0038 | 0/0 | 10655 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0039 | 0/0 | 10655 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0040 | 0/0 | 10650 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0041 | 0/0 | 10655 | 2 | 0 | 0 | 0 | 1 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0042 | 0/0 | 10676 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0043 | 0/0 | 10671 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0044 | 0/0 | 10674 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0045 | 0/0 | 10671 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0046 | 0/0 | 10664 | 2 | 0 | 1 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0047 | 0/0 | 10679 | 2 | 0 | 0 | 1 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0048 | 0/0 | 10678 | 2 | 1 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0049 | 0/0 | 10680 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0050 | 0/0 | 10683 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0051 | 0/0 | 10675 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0052 | 0/0 | 10650 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0053 | 0/0 | 10672 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0054 | 0/0 | 10673 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0055 | 0/0 | 10656 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0056 | 0/0 | 10687 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0057 | 0/0 | 10659 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0058 | 0/0 | 10660 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0059 | 0/0 | 10660 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0060 | 0/0 | 10682 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0061 | 0/0 | 10682 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0062 | 0/0 | 10684 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0063 | 0/0 | 10683 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0064 | 0/0 | 10684 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0065 | 0/0 | 10683 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0066 | 0/0 | 10685 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0067 | 0/0 | 10684 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0068 | 0/0 | 10688 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0069 | 0/0 | 10689 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0070 | 0/0 | 10688 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0071 | 0/0 | 10690 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0072 | 0/0 | 10659 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0073 | 0/1 | 10654 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0074 | 0/0 | 10651 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0075 | 0/0 | 10655 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0076 | 0/0 | 10654 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0077 | 0/0 | 10653 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0078 | 0/0 | 10655 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0079 | 0/0 | 10654 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0080 | 0/0 | 10655 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0081 | 0/0 | 10656 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0082 | 0/0 | 10657 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0083 | 0/0 | 10656 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0084 | 0/0 | 10657 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0085 | 0/0 | 10657 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0086 | 0/0 | 10658 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0087 | 0/0 | 10659 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0088 | 0/0 | 10655 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0089 | 0/0 | 10656 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0090 | 0/0 | 10656 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0091 | 0/0 | 10654 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0092 | 0/0 | 10655 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0093 | 0/0 | 10655 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0094 | 0/0 | 10661 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0095 | 0/0 | 10656 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0096 | 0/0 | 10656 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0097 | 0/0 | 10655 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0098 | 0/0 | 10653 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0099 | 0/0 | 10654 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0100 | 0/0 | 10656 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0101 | 0/0 | 10655 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0102 | 0/0 | 10655 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0103 | 0/0 | 10655 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0104 | 0/0 | 10655 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0105 | 0/0 | 10656 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0106 | 0/0 | 10656 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0107 | 0/0 | 10655 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0108 | 0/0 | 10656 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0109 | 0/0 | 10658 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0110 | 0/0 | 10660 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0111 | 0/0 | 10655 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0112 | 0/0 | 10655 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0113 | 0/0 | 10672 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0114 | 0/0 | 10658 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0115 | 0/0 | 10659 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0116 | 0/0 | 10678 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0117 | 0/0 | 10677 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0118 | 0/0 | 10678 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0119 | 0/0 | 10679 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0120 | 0/0 | 10678 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0121 | 0/0 | 10680 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0122 | 0/0 | 10671 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0123 | 0/0 | 10673 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0124 | 0/0 | 10659 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0125 | 0/0 | 10659 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0126 | 0/0 | 10660 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0127 | 0/0 | 10671 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0128 | 0/0 | 10673 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0129 | 0/0 | 10672 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0130 | 0/0 | 10673 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0131 | 0/0 | 10673 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0132 | 0/0 | 10674 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0133 | 0/0 | 10673 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0134 | 0/0 | 10674 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0135 | 0/0 | 10676 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0136 | 0/0 | 10677 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0137 | 0/0 | 10675 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0138 | 0/0 | 10677 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0139 | 0/0 | 10678 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0140 | 0/0 | 10669 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0141 | 0/0 | 10677 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0142 | 0/0 | 10683 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0143 | 0/0 | 10677 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0144 | 0/0 | 10678 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0145 | 0/0 | 10678 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0146 | 0/0 | 10677 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0147 | 0/0 | 10678 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0148 | 0/0 | 10680 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0149 | 0/0 | 10679 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0150 | 0/0 | 10678 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0151 | 0/0 | 10679 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0152 | 0/0 | 10679 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0153 | 0/0 | 10680 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0154 | 0/0 | 10681 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0155 | 0/0 | 10677 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0156 | 0/0 | 10681 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0157 | 0/0 | 10679 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0158 | 0/0 | 10681 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0159 | 0/0 | 10681 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0160 | 0/0 | 10684 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0161 | 0/0 | 10682 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0162 | 0/0 | 10684 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0163 | 0/0 | 10673 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0164 | 0/0 | 10678 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0165 | 0/0 | 10677 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0166 | 0/0 | 10679 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0167 | 0/0 | 10656 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
t0168 | 0/0 | 10679 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 16 | 0 | 13 | 0 | 3 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0002 | 0/0 | 13 | 0 | 3 | 8 | 0 | 2 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0003 | 0/1 | 9 | 0 | 0 | 5 | 0 | 3 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0004 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0008 | 0/0 | 5 | 0 | 0 | 0 | 0 | 5 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0010 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0020 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0022 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2349 | 386 | 86 | 60 | 182 | 12 | 44 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0003 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0002c0002 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 13002 | 31 | 3 | 1 | 25 | 0 | 2 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0002 | 1/0 | 13003 | 26 | 6 | 10 | 0 | 3 | 6 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0003 | 0/0 | 13027 | 22 | 1 | 5 | 14 | 1 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0004 | 0/0 | 13026 | 18 | 2 | 1 | 14 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0005 | 0/0 | 13021 | 16 | 2 | 2 | 10 | 0 | 2 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0006 | 0/0 | 13022 | 11 | 3 | 1 | 7 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0007 | 0/0 | 13004 | 9 | 0 | 9 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0008 | 0/0 | 13003 | 8 | 2 | 0 | 5 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0009 | 0/0 | 13003 | 8 | 0 | 0 | 7 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0010 | 0/0 | 13028 | 7 | 0 | 3 | 3 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0011 | 0/0 | 13002 | 5 | 2 | 1 | 0 | 2 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0012 | 0/0 | 13020 | 5 | 0 | 0 | 5 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0013 | 0/0 | 13023 | 5 | 0 | 1 | 4 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0014 | 0/0 | 13010 | 4 | 3 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0015 | 0/0 | 13002 | 4 | 2 | 0 | 0 | 0 | 2 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0016 | 0/0 | 13019 | 4 | 2 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0017 | 0/0 | 13020 | 4 | 2 | 1 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0018 | 0/0 | 13028 | 4 | 0 | 0 | 4 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0019 | 0/0 | 13029 | 4 | 0 | 1 | 2 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0020 | 0/0 | 13009 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0021 | 0/0 | 13010 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0022 | 0/0 | 12998 | 3 | 1 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0023 | 0/0 | 13002 | 3 | 0 | 0 | 0 | 0 | 3 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0024 | 0/0 | 13003 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0025 | 0/0 | 13005 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0026 | 0/0 | 13003 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0027 | 0/0 | 13003 | 3 | 1 | 1 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0028 | 0/0 | 13004 | 3 | 1 | 1 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0029 | 0/0 | 13026 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0030 | 0/0 | 13003 | 2 | 0 | 1 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0031 | 0/0 | 13008 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0032 | 0/0 | 13008 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0033 | 0/0 | 13010 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0034 | 0/0 | 13031 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0035 | 0/0 | 13032 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0036 | 0/0 | 13037 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0037 | 0/0 | 13033 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0038 | 0/0 | 13003 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0039 | 0/0 | 13003 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0040 | 0/0 | 12998 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0041 | 0/0 | 13003 | 2 | 0 | 0 | 0 | 1 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0042 | 0/0 | 13024 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0043 | 0/0 | 13019 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0044 | 0/0 | 13022 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0045 | 0/0 | 13019 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0046 | 0/0 | 13012 | 2 | 0 | 1 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0047 | 0/0 | 13027 | 2 | 0 | 0 | 1 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0048 | 0/0 | 13026 | 2 | 1 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0049 | 0/0 | 13028 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0050 | 0/0 | 13031 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0051 | 0/0 | 13023 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0052 | 0/0 | 12998 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0053 | 0/0 | 13020 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0054 | 0/0 | 13021 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0055 | 0/0 | 13004 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0056 | 0/0 | 13035 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0057 | 0/0 | 13007 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0058 | 0/0 | 13008 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0059 | 0/0 | 13008 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0060 | 0/0 | 13030 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0061 | 0/0 | 13030 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0062 | 0/0 | 13032 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0063 | 0/0 | 13031 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0064 | 0/0 | 13032 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0065 | 0/0 | 13031 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0066 | 0/0 | 13033 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0067 | 0/0 | 13032 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0068 | 0/0 | 13036 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0069 | 0/0 | 13037 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0070 | 0/0 | 13036 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0071 | 0/0 | 13038 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0072 | 0/0 | 13007 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0073 | 0/1 | 13002 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0074 | 0/0 | 12999 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0075 | 0/0 | 13003 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0076 | 0/0 | 13002 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0077 | 0/0 | 13001 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0078 | 0/0 | 13003 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0079 | 0/0 | 13002 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0080 | 0/0 | 13003 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0081 | 0/0 | 13004 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0082 | 0/0 | 13005 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0083 | 0/0 | 13004 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0084 | 0/0 | 13005 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0085 | 0/0 | 13005 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0086 | 0/0 | 13006 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0087 | 0/0 | 13007 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0088 | 0/0 | 13003 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0089 | 0/0 | 13004 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0090 | 0/0 | 13004 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0091 | 0/0 | 13002 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0092 | 0/0 | 13003 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0093 | 0/0 | 13003 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0094 | 0/0 | 13009 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0095 | 0/0 | 13004 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0096 | 0/0 | 13004 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0097 | 0/0 | 13003 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0098 | 0/0 | 13001 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0099 | 0/0 | 13002 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0100 | 0/0 | 13004 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0101 | 0/0 | 13003 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0102 | 0/0 | 13003 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0103 | 0/0 | 13003 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0104 | 0/0 | 13003 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0105 | 0/0 | 13004 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0106 | 0/0 | 13004 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0107 | 0/0 | 13003 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0108 | 0/0 | 13004 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0109 | 0/0 | 13006 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0110 | 0/0 | 13008 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0111 | 0/0 | 13003 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0112 | 0/0 | 13003 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0113 | 0/0 | 13020 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0114 | 0/0 | 13006 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0115 | 0/0 | 13007 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0116 | 0/0 | 13026 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0117 | 0/0 | 13025 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0118 | 0/0 | 13026 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0119 | 0/0 | 13027 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0120 | 0/0 | 13026 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0121 | 0/0 | 13028 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0122 | 0/0 | 13019 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0123 | 0/0 | 13021 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0124 | 0/0 | 13007 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0125 | 0/0 | 13007 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0126 | 0/0 | 13008 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0127 | 0/0 | 13019 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0128 | 0/0 | 13021 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0129 | 0/0 | 13020 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0130 | 0/0 | 13021 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0131 | 0/0 | 13021 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0132 | 0/0 | 13022 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0133 | 0/0 | 13021 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0134 | 0/0 | 13022 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0135 | 0/0 | 13024 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0136 | 0/0 | 13025 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0137 | 0/0 | 13023 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0138 | 0/0 | 13025 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0139 | 0/0 | 13026 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0140 | 0/0 | 13017 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0141 | 0/0 | 13025 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0142 | 0/0 | 13031 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0143 | 0/0 | 13025 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0144 | 0/0 | 13026 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0145 | 0/0 | 13026 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0146 | 0/0 | 13025 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0147 | 0/0 | 13026 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0148 | 0/0 | 13028 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0149 | 0/0 | 13027 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0150 | 0/0 | 13026 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0151 | 0/0 | 13027 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0152 | 0/0 | 13027 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0153 | 0/0 | 13028 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0154 | 0/0 | 13029 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0155 | 0/0 | 13025 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0156 | 0/0 | 13029 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0157 | 0/0 | 13027 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0158 | 0/0 | 13029 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0159 | 0/0 | 13029 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0160 | 0/0 | 13032 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0161 | 0/0 | 13030 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0162 | 0/0 | 13032 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0163 | 0/0 | 13021 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0164 | 0/0 | 13026 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0165 | 0/0 | 13025 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0166 | 0/0 | 13027 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0167 | 0/0 | 13004 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0001t0168 | 0/0 | 13027 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0001c0003t0037 | 0/0 | 13033 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
a0002c0002t0010 | 0/0 | 13028 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | copy fasta | chr14 | 92116969 | 92177145 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0002g0020 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0002g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0002g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0002g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0004g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0005g0002 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0005g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0006g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0006g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0006g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0006g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0006g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0007g0001 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0007g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0008g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0008g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0008g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0008g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0008g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0008g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0009g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0009g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0009g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0009g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0009g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0009g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0009g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0010g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0010g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0010g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0010g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0010g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0010g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0010g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0011g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0011g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0011g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0011g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0012g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0012g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0012g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0013g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0013g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0013g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0013g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0013g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0014g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0014g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0014g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0014g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0015g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0015g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0015g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0016g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0016g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0016g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0016g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0017g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0017g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0017g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0018g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0018g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0018g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0018g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0019g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0019g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0019g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0019g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0020g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0021g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0021g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0021g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0022g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0022g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0022g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0023g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0023g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0024g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0024g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0024g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0025g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0025g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0025g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0026g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0026g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0026g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0027g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0027g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0027g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0028g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0028g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0028g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0029g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0029g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0029g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0030g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0030g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0031g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0032g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0033g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0033g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0034g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0034g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0035g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0036g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0036g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0037g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0038g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0038g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0039g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0040g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0041g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0041g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0042g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0042g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0043g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0044g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0044g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0045g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0045g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0046g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0046g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0047g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0047g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0048g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0048g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0049g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0049g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0050g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0050g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0051g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0052g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0053g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0054g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0055g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0056g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0057g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0058g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0059g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0060g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0061g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0062g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0063g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0064g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0065g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0066g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0067g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0068g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0069g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0070g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0071g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0072g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0073g0003 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0074g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0075g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0076g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0077g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0078g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0079g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0080g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0081g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0082g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0083g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0084g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0085g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0086g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0087g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0088g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0089g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0090g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0091g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0092g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0093g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0094g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0095g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0096g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0097g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0098g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0099g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0100g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0101g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0102g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0103g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0104g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0105g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0106g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0107g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0108g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0109g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0110g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0111g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0112g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0113g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0114g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0115g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0116g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0117g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0118g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0119g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0120g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0121g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0122g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0123g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0124g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0125g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0126g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0127g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0128g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0129g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0130g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0131g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0132g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0133g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0134g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0135g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0136g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0137g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0138g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0139g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0140g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0141g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0142g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0143g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0144g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0145g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0146g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0147g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0148g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0149g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0150g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0151g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0152g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0153g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0154g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0155g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0156g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0157g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0158g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0159g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0160g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0161g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0162g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0163g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0164g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0165g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0166g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0167g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0001t0168g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0001c0003t0037g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
a0002c0002t0010g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0041 | g0001 | EUR | GBR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0043 | EUR | GBR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00140 | hp1 | a0001 | c0001 | t0004 | g0077 | EUR | GBR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00140 | hp2 | a0001 | c0001 | t0027 | g0236 | EUR | GBR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00323 | hp1 | a0001 | c0001 | t0167 | g0045 | EUR | FIN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0022 | EUR | FIN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00408 | hp1 | a0001 | c0001 | t0012 | g0002 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00408 | hp2 | a0001 | c0001 | t0021 | g0126 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00423 | hp1 | a0001 | c0001 | t0077 | g0156 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00423 | hp2 | a0001 | c0001 | t0162 | g0009 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00438 | hp2 | a0001 | c0001 | t0145 | g0083 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00544 | hp1 | a0001 | c0001 | t0018 | g0076 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0096 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00558 | hp2 | a0001 | c0001 | t0053 | g0213 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00609 | hp1 | a0001 | c0001 | t0004 | g0095 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00621 | hp1 | a0001 | c0001 | t0051 | g0014 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00621 | hp2 | a0001 | c0001 | t0009 | g0163 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0085 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00642 | hp2 | a0001 | c0001 | t0108 | g0226 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00673 | hp1 | a0001 | c0001 | t0138 | g0195 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00735 | hp1 | a0001 | c0001 | t0055 | g0001 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00735 | hp2 | a0001 | c0001 | t0027 | g0234 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00738 | hp1 | a0001 | c0001 | t0104 | g0043 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG00738 | hp2 | a0001 | c0001 | t0098 | g0001 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01069 | hp1 | a0001 | c0001 | t0049 | g0090 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01069 | hp2 | a0001 | c0001 | t0030 | g0240 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01071 | hp1 | a0001 | c0001 | t0049 | g0079 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01071 | hp2 | a0001 | c0001 | t0011 | g0244 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01074 | hp1 | a0001 | c0001 | t0013 | g0212 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01074 | hp2 | a0001 | c0001 | t0010 | g0010 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01081 | hp1 | a0001 | c0001 | t0010 | g0114 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01099 | hp2 | a0001 | c0001 | t0046 | g0068 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01106 | hp2 | a0001 | c0001 | t0010 | g0063 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01109 | hp1 | a0001 | c0001 | t0028 | g0001 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01109 | hp2 | a0001 | c0001 | t0014 | g0246 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01167 | hp2 | a0001 | c0001 | t0129 | g0215 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01168 | hp2 | a0001 | c0001 | t0166 | g0103 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01175 | hp2 | a0001 | c0001 | t0109 | g0242 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01192 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01192 | hp2 | a0001 | c0001 | t0096 | g0047 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01255 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01255 | hp2 | a0001 | c0001 | t0074 | g0038 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01256 | hp1 | a0001 | c0001 | t0017 | g0002 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01256 | hp2 | a0001 | c0001 | t0111 | g0001 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0071 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01258 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01346 | hp1 | a0001 | c0001 | t0045 | g0196 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01361 | hp1 | a0001 | c0001 | t0105 | g0022 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01361 | hp2 | a0001 | c0001 | t0142 | g0054 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01433 | hp1 | a0001 | c0001 | t0007 | g0044 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0107 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01496 | hp2 | a0001 | c0001 | t0123 | g0191 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0026 | EUR | IBS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01515 | hp2 | a0001 | c0001 | t0011 | g0001 | EUR | IBS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01517 | hp1 | a0001 | c0001 | t0011 | g0022 | EUR | IBS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01517 | hp2 | a0001 | c0001 | t0047 | g0026 | EUR | IBS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01884 | hp1 | a0001 | c0001 | t0122 | g0256 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01891 | hp1 | a0001 | c0001 | t0148 | g0134 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01934 | hp1 | a0001 | c0001 | t0007 | g0044 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01934 | hp2 | a0001 | c0001 | t0156 | g0074 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01975 | hp1 | a0001 | c0001 | t0045 | g0197 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01975 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01978 | hp1 | a0001 | c0001 | t0006 | g0217 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01978 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG01981 | hp2 | a0001 | c0001 | t0147 | g0030 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02015 | hp1 | a0001 | c0001 | t0079 | g0158 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02015 | hp2 | a0001 | c0001 | t0163 | g0014 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0203 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02027 | hp2 | a0001 | c0001 | t0155 | g0075 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02040 | hp1 | a0001 | c0001 | t0009 | g0143 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02040 | hp2 | a0001 | c0001 | t0020 | g0011 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02055 | hp1 | a0001 | c0001 | t0086 | g0037 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02055 | hp2 | a0001 | c0001 | t0124 | g0245 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02080 | hp2 | a0001 | c0001 | t0137 | g0204 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02083 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02135 | hp1 | a0001 | c0001 | t0019 | g0094 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02135 | hp2 | a0001 | c0001 | t0038 | g0013 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02145 | hp1 | a0001 | c0001 | t0102 | g0235 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02145 | hp2 | a0001 | c0001 | t0121 | g0258 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02148 | hp1 | a0001 | c0001 | t0019 | g0086 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02148 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02155 | hp1 | a0001 | c0001 | t0051 | g0014 | EAS | CDX | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02155 | hp2 | a0001 | c0001 | t0039 | g0003 | EAS | CDX | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02165 | hp1 | a0001 | c0001 | t0021 | g0004 | EAS | CDX | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02165 | hp2 | a0001 | c0001 | t0140 | g0024 | EAS | CDX | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02257 | hp1 | a0001 | c0001 | t0095 | g0224 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02257 | hp2 | a0001 | c0001 | t0094 | g0247 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02258 | hp1 | a0001 | c0001 | t0040 | g0034 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02258 | hp2 | a0001 | c0001 | t0106 | g0049 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02273 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02280 | hp1 | a0001 | c0001 | t0017 | g0201 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02293 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02451 | hp1 | a0001 | c0001 | t0025 | g0176 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0218 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02523 | hp1 | a0001 | c0001 | t0070 | g0032 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02572 | hp1 | a0001 | c0001 | t0008 | g0148 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02602 | hp1 | a0001 | c0001 | t0134 | g0207 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02602 | hp2 | a0001 | c0001 | t0064 | g0122 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02615 | hp1 | a0001 | c0001 | t0025 | g0037 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02615 | hp2 | a0001 | c0001 | t0017 | g0007 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02622 | hp1 | a0001 | c0001 | t0029 | g0135 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02630 | hp1 | a0001 | c0001 | t0015 | g0021 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02647 | hp1 | a0001 | c0001 | t0040 | g0034 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02647 | hp2 | a0001 | c0001 | t0027 | g0047 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02683 | hp1 | a0001 | c0001 | t0046 | g0111 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02698 | hp1 | a0001 | c0001 | t0023 | g0003 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02698 | hp2 | a0001 | c0001 | t0030 | g0239 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02717 | hp2 | a0001 | c0001 | t0130 | g0208 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0262 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02735 | hp2 | a0001 | c0001 | t0017 | g0002 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02738 | hp1 | a0001 | c0001 | t0056 | g0128 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02809 | hp1 | a0001 | c0001 | t0016 | g0193 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02809 | hp2 | a0001 | c0001 | t0113 | g0253 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02895 | hp1 | a0001 | c0001 | t0043 | g0042 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02895 | hp2 | a0001 | c0001 | t0115 | g0255 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02896 | hp1 | a0001 | c0001 | t0043 | g0042 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02896 | hp2 | a0001 | c0001 | t0014 | g0248 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02897 | hp1 | a0001 | c0001 | t0114 | g0254 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02897 | hp2 | a0001 | c0001 | t0014 | g0250 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02922 | hp1 | a0001 | c0001 | t0117 | g0023 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02922 | hp2 | a0001 | c0001 | t0100 | g0243 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02965 | hp1 | a0001 | c0001 | t0165 | g0259 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02965 | hp2 | a0001 | c0001 | t0025 | g0175 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02970 | hp1 | a0001 | c0001 | t0119 | g0023 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02976 | hp1 | a0001 | c0001 | t0084 | g0172 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02976 | hp2 | a0001 | c0001 | t0044 | g0007 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03041 | hp2 | a0001 | c0001 | t0026 | g0153 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03098 | hp1 | a0001 | c0001 | t0082 | g0182 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03098 | hp2 | a0001 | c0001 | t0087 | g0177 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03130 | hp1 | a0001 | c0001 | t0097 | g0241 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03130 | hp2 | a0001 | c0001 | t0133 | g0192 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03139 | hp1 | a0001 | c0001 | t0022 | g0038 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03195 | hp1 | a0001 | c0001 | t0011 | g0046 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03195 | hp2 | a0001 | c0001 | t0029 | g0140 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03209 | hp1 | a0001 | c0001 | t0042 | g0257 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03209 | hp2 | a0001 | c0001 | t0048 | g0137 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03225 | hp1 | a0001 | c0001 | t0011 | g0046 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03225 | hp2 | a0001 | c0001 | t0026 | g0150 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03239 | hp1 | a0001 | c0001 | t0041 | g0048 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03239 | hp2 | a0001 | c0001 | t0023 | g0003 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03453 | hp1 | a0001 | c0001 | t0110 | g0228 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03453 | hp2 | a0001 | c0001 | t0044 | g0194 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03486 | hp1 | a0001 | c0001 | t0118 | g0261 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03490 | hp1 | a0001 | c0001 | t0048 | g0113 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03491 | hp1 | a0001 | c0001 | t0065 | g0121 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03491 | hp2 | a0001 | c0001 | t0015 | g0048 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03492 | hp2 | a0001 | c0001 | t0061 | g0004 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03540 | hp2 | a0001 | c0001 | t0127 | g0205 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03579 | hp1 | a0001 | c0001 | t0116 | g0023 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03579 | hp2 | a0001 | c0001 | t0015 | g0021 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03654 | hp1 | a0001 | c0001 | t0019 | g0112 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03669 | hp1 | a0001 | c0001 | t0028 | g0251 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03669 | hp2 | a0001 | c0001 | t0101 | g0008 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0220 | SAS | STU | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03688 | hp2 | a0001 | c0001 | t0159 | g0084 | SAS | STU | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03704 | hp1 | a0001 | c0001 | t0080 | g0174 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03704 | hp2 | a0001 | c0001 | t0067 | g0119 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03710 | hp1 | a0001 | c0001 | t0005 | g0200 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03710 | hp2 | a0001 | c0001 | t0005 | g0199 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03831 | hp1 | a0001 | c0001 | t0132 | g0202 | SAS | BEB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03831 | hp2 | a0001 | c0001 | t0009 | g0003 | SAS | BEB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | BEB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03834 | hp2 | a0001 | c0001 | t0146 | g0056 | SAS | BEB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03942 | hp1 | a0001 | c0001 | t0131 | g0187 | SAS | BEB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03942 | hp2 | a0001 | c0001 | t0112 | g0232 | SAS | BEB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG04115 | hp1 | a0001 | c0001 | t0015 | g0225 | SAS | STU | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG04115 | hp2 | a0001 | c0001 | t0083 | g0165 | SAS | STU | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG04184 | hp1 | a0001 | c0001 | t0136 | g0019 | SAS | BEB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG04184 | hp2 | a0001 | c0001 | t0139 | g0082 | SAS | BEB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG04199 | hp1 | a0001 | c0001 | t0008 | g0185 | SAS | STU | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG04199 | hp2 | a0001 | c0001 | t0103 | g0238 | SAS | STU | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG04204 | hp1 | a0001 | c0001 | t0023 | g0035 | SAS | STU | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG04204 | hp2 | a0001 | c0001 | t0126 | g0002 | SAS | STU | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18522 | hp1 | a0001 | c0001 | t0052 | g0039 | AFR | YRI | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0206 | AFR | YRI | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18612 | hp1 | a0001 | c0001 | t0063 | g0118 | EAS | CHB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | CHB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18747 | hp2 | a0001 | c0001 | t0006 | g0210 | EAS | CHB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18906 | hp1 | a0001 | c0001 | t0093 | g0152 | AFR | YRI | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18906 | hp2 | a0001 | c0001 | t0042 | g0252 | AFR | YRI | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18939 | hp1 | a0001 | c0001 | t0143 | g0009 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18939 | hp2 | a0001 | c0001 | t0005 | g0219 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18941 | hp1 | a0001 | c0001 | t0128 | g0209 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18941 | hp2 | a0001 | c0001 | t0150 | g0091 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18942 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18942 | hp2 | a0001 | c0001 | t0078 | g0035 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18945 | hp1 | a0001 | c0001 | t0058 | g0004 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18946 | hp1 | a0001 | c0001 | t0068 | g0125 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18948 | hp1 | a0001 | c0001 | t0033 | g0117 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18948 | hp2 | a0001 | c0001 | t0012 | g0019 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18949 | hp2 | a0001 | c0001 | t0006 | g0211 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18950 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18950 | hp2 | a0001 | c0001 | t0036 | g0031 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18951 | hp1 | a0001 | c0001 | t0022 | g0006 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18952 | hp1 | a0001 | c0001 | t0020 | g0011 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18952 | hp2 | a0001 | c0001 | t0149 | g0029 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18953 | hp2 | a0001 | c0001 | t0144 | g0065 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18954 | hp1 | a0001 | c0001 | t0164 | g0144 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18954 | hp2 | a0001 | c0001 | t0057 | g0004 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18956 | hp1 | a0001 | c0001 | t0021 | g0127 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18956 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18957 | hp1 | a0001 | c0001 | t0008 | g0159 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18959 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18959 | hp2 | a0001 | c0001 | t0092 | g0003 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18961 | hp1 | a0001 | c0001 | t0009 | g0149 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18961 | hp2 | a0001 | c0001 | t0018 | g0073 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18962 | hp2 | a0001 | c0001 | t0038 | g0142 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18964 | hp1 | a0001 | c0001 | t0075 | g0013 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18964 | hp2 | a0001 | c0003 | t0037 | g0004 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18965 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18966 | hp1 | a0001 | c0001 | t0008 | g0155 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18968 | hp2 | a0001 | c0001 | t0024 | g0157 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18969 | hp1 | a0001 | c0001 | t0008 | g0036 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18971 | hp1 | a0001 | c0001 | t0031 | g0004 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18971 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18972 | hp1 | a0001 | c0001 | t0135 | g0189 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18972 | hp2 | a0001 | c0001 | t0024 | g0017 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18977 | hp2 | a0001 | c0001 | t0050 | g0027 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18979 | hp1 | a0001 | c0001 | t0010 | g0028 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18980 | hp1 | a0001 | c0001 | t0034 | g0031 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18980 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18981 | hp1 | a0001 | c0001 | t0018 | g0062 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18981 | hp2 | a0001 | c0001 | t0013 | g0040 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18982 | hp1 | a0001 | c0001 | t0072 | g0120 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18982 | hp2 | a0001 | c0001 | t0016 | g0131 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18984 | hp1 | a0001 | c0001 | t0157 | g0106 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18984 | hp2 | a0001 | c0001 | t0009 | g0145 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18986 | hp2 | a0001 | c0001 | t0013 | g0186 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18988 | hp1 | a0001 | c0001 | t0154 | g0093 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18988 | hp2 | a0001 | c0001 | t0125 | g0190 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18989 | hp1 | a0001 | c0001 | t0032 | g0033 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18989 | hp2 | a0001 | c0001 | t0006 | g0018 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18991 | hp2 | a0001 | c0001 | t0054 | g0214 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18993 | hp1 | a0001 | c0001 | t0009 | g0006 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18993 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18995 | hp1 | a0001 | c0001 | t0089 | g0017 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18997 | hp1 | a0001 | c0001 | t0066 | g0115 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18998 | hp1 | a0001 | c0001 | t0009 | g0006 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18998 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA18999 | hp2 | a0001 | c0001 | t0016 | g0132 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19000 | hp2 | a0001 | c0001 | t0013 | g0216 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19001 | hp1 | a0001 | c0001 | t0158 | g0069 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19001 | hp2 | a0001 | c0001 | t0032 | g0033 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19003 | hp1 | a0001 | c0001 | t0037 | g0129 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19003 | hp2 | a0001 | c0001 | t0151 | g0064 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19007 | hp1 | a0001 | c0001 | t0033 | g0032 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19007 | hp2 | a0001 | c0001 | t0010 | g0100 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19009 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19009 | hp2 | a0001 | c0001 | t0035 | g0016 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19010 | hp1 | a0001 | c0001 | t0050 | g0102 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19011 | hp1 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19011 | hp2 | a0001 | c0001 | t0024 | g0005 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19030 | hp1 | a0001 | c0001 | t0085 | g0154 | AFR | LWK | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19030 | hp2 | a0001 | c0001 | t0029 | g0136 | AFR | LWK | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19054 | hp1 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19054 | hp2 | a0001 | c0001 | t0071 | g0004 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19055 | hp1 | a0001 | c0001 | t0088 | g0160 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19055 | hp2 | a0001 | c0001 | t0060 | g0116 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19056 | hp1 | a0001 | c0001 | t0012 | g0130 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19056 | hp2 | a0001 | c0001 | t0107 | g0233 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19057 | hp1 | a0001 | c0001 | t0008 | g0036 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19058 | hp1 | a0001 | c0001 | t0062 | g0123 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19058 | hp2 | a0001 | c0001 | t0022 | g0005 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19060 | hp1 | a0001 | c0001 | t0034 | g0105 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19060 | hp2 | a0001 | c0001 | t0039 | g0003 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19062 | hp1 | a0001 | c0001 | t0012 | g0019 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19063 | hp2 | a0001 | c0001 | t0160 | g0067 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19064 | hp1 | a0001 | c0001 | t0091 | g0012 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19064 | hp2 | a0001 | c0001 | t0020 | g0011 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19065 | hp2 | a0001 | c0001 | t0152 | g0015 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19066 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19066 | hp2 | a0001 | c0001 | t0010 | g0097 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19074 | hp1 | a0001 | c0001 | t0069 | g0124 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19074 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19075 | hp1 | a0001 | c0001 | t0168 | g0087 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19077 | hp1 | a0002 | c0002 | t0010 | g0078 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19079 | hp1 | a0001 | c0001 | t0036 | g0016 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19080 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19081 | hp1 | a0001 | c0001 | t0081 | g0013 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19081 | hp2 | a0001 | c0001 | t0047 | g0092 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19083 | hp1 | a0001 | c0001 | t0035 | g0016 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19083 | hp2 | a0001 | c0001 | t0013 | g0188 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19084 | hp1 | a0001 | c0001 | t0031 | g0004 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19087 | hp1 | a0001 | c0001 | t0153 | g0024 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19088 | hp1 | a0001 | c0001 | t0019 | g0098 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19088 | hp2 | a0001 | c0001 | t0006 | g0018 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19090 | hp1 | a0001 | c0001 | t0018 | g0010 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19090 | hp2 | a0001 | c0001 | t0009 | g0005 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19091 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19091 | hp2 | a0001 | c0001 | t0059 | g0011 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19240 | hp1 | a0001 | c0001 | t0008 | g0173 | AFR | YRI | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0133 | AFR | YRI | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA20129 | hp1 | a0001 | c0001 | t0141 | g0139 | AFR | ASW | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA20129 | hp2 | a0001 | c0001 | t0120 | g0260 | AFR | ASW | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA20752 | hp2 | a0001 | c0001 | t0010 | g0080 | EUR | TSI | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | GIH | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA20905 | hp2 | a0001 | c0001 | t0076 | g0166 | SAS | GIH | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02486 | hp1 | a0001 | c0001 | t0099 | g0227 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02486 | hp2 | a0001 | c0001 | t0026 | g0151 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02559 | hp1 | a0001 | c0001 | t0014 | g0249 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG02559 | hp2 | a0001 | c0001 | t0028 | g0231 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03471 | hp1 | a0001 | c0001 | t0090 | g0178 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG03471 | hp2 | a0001 | c0001 | t0016 | g0198 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG06807 | hp1 | a0001 | c0001 | t0052 | g0039 | AFR | USA | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | USA | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | USA | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
NA20300 | hp2 | a0001 | c0001 | t0161 | g0030 | AFR | USA | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0073 | g0003 | REF | REF | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0237 | REF | REF | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:92156503
|
G | C | 1 | a0002 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.1467G>C | p.Glu489Asp | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/16 | 1720/13003 | 1467/2349 | 489/782 | chr14 | 92156503 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:92157767
|
A | G | 1 | a0001c0003 | 1 | NA18964.hp2 | synonymous_variant | LOW | c.1704A>G | p.Pro568Pro | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/16 | 1957/13003 | 1704/2349 | 568/782 | chr14 | 92157767 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:92121972
|
A | G | 1 | a0001c0001t0168 | 1 | NA19075.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-250A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/16 | chr14 | 92121972 | ||||||
chr14:92122070
|
C | T | 1 | a0001c0001t0052 | 2 | HG06807.hp1 NA18522.hp1 |
5_prime_UTR_variant | MODIFIER | c.-152C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/16 | 8915 | chr14 | 92122070 | |||||
chr14:92161944
|
G | A | 2 | a0001c0001t0053a0001c0001t0054 | 2 | HG00558.hp2 NA18991.hp2 |
3_prime_UTR_variant | MODIFIER | c.*200G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 200 | chr14 | 92161944 | |||||
chr14:92162012
|
T | C | 1 | a0001c0001t0030 | 2 | HG01069.hp2 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*268T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 268 | chr14 | 92162012 | |||||
chr14:92162110
|
G | A | 1 | a0001c0001t0055 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*366G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 366 | chr14 | 92162110 | |||||
chr14:92162272
|
G | A | 1 | a0001c0001t0031 | 2 | NA18971.hp1 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*528G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 528 | chr14 | 92162272 | |||||
chr14:92162315
|
A | G | 1 | a0001c0001t0167 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*571A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 571 | chr14 | 92162315 | |||||
chr14:92162339
|
A | G | 1 | a0001c0001t0166 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*595A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 595 | chr14 | 92162339 | |||||
chr14:92162404
|
A | G | 1 | a0001c0001t0165 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*660A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 660 | chr14 | 92162404 | |||||
chr14:92162534
|
G | A | 27 | a0001c0001t0020a0001c0001t0021a0001c0001t0031others(24): Show | 37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*790G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 790 | chr14 | 92162534 | |||||
chr14:92162608
|
T | G | 33 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(30): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*864T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 864 | chr14 | 92162608 | |||||
chr14:92162974
|
G | T | 1 | a0001c0001t0164 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1230G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1230 | chr14 | 92162974 | |||||
chr14:92163008
|
A | G | 1 | a0001c0001t0040 | 2 | HG02258.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1264A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1264 | chr14 | 92163008 | |||||
chr14:92163044
|
C | T | 2 | a0001c0001t0026a0001c0001t0093 | 4 | HG02486.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1300C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1300 | chr14 | 92163044 | |||||
chr14:92163337
|
C | A | 2 | a0001c0001t0014a0001c0001t0094 | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1593C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1593 | chr14 | 92163337 | |||||
chr14:92163366
|
C | T | 2 | a0001c0001t0051a0001c0001t0163 | 3 | HG00621.hp1 HG02015.hp2 HG02155.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1622C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1622 | chr14 | 92163366 | |||||
chr14:92163371
|
T | TAAAC | 76 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(73): Show | 181 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*1630_*1631insCAAA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1631 | INFO_REALIGN_3_PRIME | chr14 | 92163371 | ||||
chr14:92163373
|
A | AACAC | 63 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(60): Show | 130 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*1630_*1631insCACA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1631 | INFO_REALIGN_3_PRIME | chr14 | 92163373 | ||||
chr14:92163374
|
A | AC | 3 | a0001c0001t0037a0001c0001t0072a0001c0003t0037 | 3 | NA18964.hp2 NA18982.hp1 NA19003.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1630_*1631insC | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1631 | chr14 | 92163374 | |||||
chr14:92163378
|
A | G | 1 | a0001c0001t0092 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1634A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1634 | chr14 | 92163378 | |||||
chr14:92163379
|
T | C | 3 | a0001c0001t0037a0001c0001t0072a0001c0003t0037 | 3 | NA18964.hp2 NA18982.hp1 NA19003.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1635T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1635 | chr14 | 92163379 | |||||
chr14:92163420
|
T | A | 1 | a0001c0001t0095 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1676T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1676 | chr14 | 92163420 | |||||
chr14:92163445
|
T | C | 1 | a0001c0001t0073 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1701T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1701 | chr14 | 92163445 | |||||
chr14:92163472
|
T | C | 12 | a0001c0001t0042a0001c0001t0113a0001c0001t0114others(9): Show | 13 | HG01884.hp1 HG02145.hp2 HG02809.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1728T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1728 | chr14 | 92163472 | |||||
chr14:92163563
|
A | G | 2 | a0001c0001t0014a0001c0001t0094 | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1819A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1819 | chr14 | 92163563 | |||||
chr14:92163599
|
A | G | 1 | a0001c0001t0091 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1855A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1855 | chr14 | 92163599 | |||||
chr14:92163635
|
C | T | 78 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(75): Show | 146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*1891C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1891 | chr14 | 92163635 | |||||
chr14:92163722
|
T | G | 2 | a0001c0001t0014a0001c0001t0094 | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1978T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1978 | chr14 | 92163722 | |||||
chr14:92163807
|
C | T | 2 | a0001c0001t0041a0001c0001t0112 | 3 | HG00099.hp1 HG03239.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2063C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2063 | chr14 | 92163807 | |||||
chr14:92163834
|
G | A | 2 | a0001c0001t0027a0001c0001t0096 | 4 | HG00140.hp2 HG00735.hp2 HG01192.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2090G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2090 | chr14 | 92163834 | |||||
chr14:92163888
|
G | A | 1 | a0001c0001t0123 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2144G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2144 | chr14 | 92163888 | |||||
chr14:92163947
|
C | T | 1 | a0001c0001t0045 | 2 | HG01346.hp1 HG01975.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2203C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2203 | chr14 | 92163947 | |||||
chr14:92163982
|
G | A | 33 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(30): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*2238G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2238 | chr14 | 92163982 | |||||
chr14:92164025
|
T | C | 27 | a0001c0001t0020a0001c0001t0021a0001c0001t0031others(24): Show | 37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2281T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2281 | chr14 | 92164025 | |||||
chr14:92164063
|
C | T | 1 | a0001c0001t0112 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2319C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2319 | chr14 | 92164063 | |||||
chr14:92164226
|
C | T | 2 | a0001c0001t0014a0001c0001t0094 | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2482C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2482 | chr14 | 92164226 | |||||
chr14:92164267
|
T | G | 1 | a0001c0001t0097 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2523T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2523 | chr14 | 92164267 | |||||
chr14:92164581
|
G | T | 2 | a0001c0001t0137a0001c0001t0138 | 2 | HG00673.hp1 HG02080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2837G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2837 | chr14 | 92164581 | |||||
chr14:92164621
|
T | A | 142 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(139): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*2877T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2877 | chr14 | 92164621 | |||||
chr14:92165025
|
C | A | 1 | a0001c0001t0056 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3281C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3281 | chr14 | 92165025 | |||||
chr14:92165123
|
A | G | 1 | a0001c0001t0090 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3379A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3379 | chr14 | 92165123 | |||||
chr14:92165198
|
A | C | 1 | a0001c0001t0052 | 2 | HG06807.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3454A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3454 | chr14 | 92165198 | |||||
chr14:92165232
|
C | G | 11 | a0001c0001t0042a0001c0001t0114a0001c0001t0115others(8): Show | 12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3488C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3488 | chr14 | 92165232 | |||||
chr14:92165235
|
G | A | 1 | a0001c0001t0113 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3491G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3491 | chr14 | 92165235 | |||||
chr14:92165241
|
G | GT | 67 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(64): Show | 140 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*3510dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3511 | INFO_REALIGN_3_PRIME | chr14 | 92165241 | ||||
chr14:92165241
|
GT | G | 3 | a0001c0001t0014a0001c0001t0094a0001c0001t0163 | 6 | HG01109.hp2 HG02015.hp2 HG02257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3510delT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3510 | INFO_REALIGN_3_PRIME | chr14 | 92165241 | ||||
chr14:92165334
|
C | A | 11 | a0001c0001t0042a0001c0001t0114a0001c0001t0115others(8): Show | 12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3590C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3590 | chr14 | 92165334 | |||||
chr14:92165521
|
G | A | 1 | a0001c0001t0093 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3777G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3777 | chr14 | 92165521 | |||||
chr14:92165546
|
A | G | 2 | a0001c0001t0014a0001c0001t0094 | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3802A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3802 | chr14 | 92165546 | |||||
chr14:92165597
|
T | G | 1 | a0001c0001t0124 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3853T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3853 | chr14 | 92165597 | |||||
chr14:92165610
|
A | G | 62 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(59): Show | 163 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*3866A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3866 | chr14 | 92165610 | |||||
chr14:92165725
|
G | A | 142 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(139): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*3981G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3981 | chr14 | 92165725 | |||||
chr14:92165766
|
G | A | 2 | a0001c0001t0014a0001c0001t0094 | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4022G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4022 | chr14 | 92165766 | |||||
chr14:92165854
|
C | CT | 7 | a0001c0001t0021a0001c0001t0028a0001c0001t0072others(4): Show | 11 | HG00408.hp2 HG01109.hp1 HG01175.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4135dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTT | 17 | a0001c0001t0001a0001c0001t0008a0001c0001t0023others(14): Show | 60 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*4132_*4135dupTTTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTTT | 10 | a0001c0001t0009a0001c0001t0014a0001c0001t0025others(7): Show | 22 | HG00621.hp2 HG01109.hp2 HG02040.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4131_*4135dupTTTT others(1): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTTTT | 5 | a0001c0001t0026a0001c0001t0085a0001c0001t0086others(2): Show | 7 | HG02055.hp1 HG02486.hp2 HG03041.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4130_*4135dupTTTT others(2): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTTTTT others(2): Show |
5 | a0001c0001t0042a0001c0001t0116a0001c0001t0117others(2): Show | 6 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4127_*4135dupTTTT others(5): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0113a0001c0001t0119a0001c0001t0120 | 3 | HG02809.hp2 HG02970.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4126_*4135dupTTTT others(6): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0121 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4125_*4135dupTTTT others(7): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTTTTT others(5): Show |
5 | a0001c0001t0043a0001c0001t0122a0001c0001t0127others(2): Show | 6 | HG01361.hp2 HG01884.hp1 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4124_*4135dupTTTT others(8): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTTTTT others(6): Show |
18 | a0001c0001t0004a0001c0001t0016a0001c0001t0017others(15): Show | 45 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*4123_*4135dupTTTT others(9): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTTTTT others(7): Show |
17 | a0001c0001t0003a0001c0001t0005a0001c0001t0012others(14): Show | 62 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*4122_*4135dupTTTT others(10): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTTTTT others(8): Show |
12 | a0001c0001t0006a0001c0001t0010a0001c0001t0019others(9): Show | 31 | HG01074.hp2 HG01081.hp1 HG01106.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*4121_*4135dupTTTT others(11): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTTTTT others(9): Show |
8 | a0001c0001t0013a0001c0001t0049a0001c0001t0050others(5): Show | 15 | HG00621.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4120_*4135dupTTTT others(12): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0161 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4119_*4135dupTTTT others(13): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTTTTT others(11): Show |
3 | a0001c0001t0136a0001c0001t0138a0001c0001t0162 | 3 | HG00423.hp2 HG00673.hp1 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4118_*4135dupTTTT others(14): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTTTTT others(14): Show |
4 | a0001c0001t0060a0001c0001t0061a0001c0001t0062others(1): Show | 4 | HG03492.hp2 NA18612.hp1 NA19055.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4115_*4135dupTTTT others(17): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTTTTT others(15): Show |
3 | a0001c0001t0034a0001c0001t0064a0001c0001t0065 | 4 | HG02602.hp2 HG03491.hp1 NA18980.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4114_*4135dupTTTT others(18): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTTTTT others(16): Show |
3 | a0001c0001t0035a0001c0001t0066a0001c0001t0067 | 4 | HG03704.hp2 NA18997.hp1 NA19009.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4113_*4135dupTTTT others(19): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0056 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4112_*4135dupTTTT others(20): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0068 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4135_*4136insTTTT others(22): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTTTTT others(20): Show |
5 | a0001c0001t0037a0001c0001t0069a0001c0001t0070others(2): Show | 5 | HG02523.hp1 NA18964.hp2 NA19003.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4135_*4136insTTTT others(23): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
C | CTTTTTTT others(21): Show |
1 | a0001c0001t0036 | 2 | NA18950.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4135_*4136insTTTT others(24): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165854
|
CT | C | 4 | a0001c0001t0015a0001c0001t0046a0001c0001t0059others(1): Show | 8 | HG01099.hp2 HG01256.hp2 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4135delT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4135 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | ||||
chr14:92165892
|
T | C | 142 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(139): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*4148T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4148 | chr14 | 92165892 | |||||
chr14:92165965
|
G | T | 1 | a0001c0001t0079 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4221G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4221 | chr14 | 92165965 | |||||
chr14:92166115
|
G | T | 33 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(30): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*4371G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4371 | chr14 | 92166115 | |||||
chr14:92166146
|
G | C | 1 | a0001c0001t0113 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4402G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4402 | chr14 | 92166146 | |||||
chr14:92166406
|
G | A | 2 | a0001c0001t0014a0001c0001t0094 | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4662G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4662 | chr14 | 92166406 | |||||
chr14:92166540
|
T | G | 142 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(139): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*4796T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4796 | chr14 | 92166540 | |||||
chr14:92166682
|
T | C | 1 | a0001c0001t0159 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4938T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4938 | chr14 | 92166682 | |||||
chr14:92166843
|
T | C | 29 | a0001c0001t0005a0001c0001t0006a0001c0001t0012others(26): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*5099T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5099 | chr14 | 92166843 | |||||
chr14:92166982
|
G | A | 11 | a0001c0001t0042a0001c0001t0114a0001c0001t0115others(8): Show | 12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5238G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5238 | chr14 | 92166982 | |||||
chr14:92167014
|
C | CT | 53 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(50): Show | 117 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*5285dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5286 | INFO_REALIGN_3_PRIME | chr14 | 92167014 | ||||
chr14:92167014
|
C | CTT | 46 | a0001c0001t0005a0001c0001t0006a0001c0001t0012others(43): Show | 95 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*5284_*5285dupTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5286 | INFO_REALIGN_3_PRIME | chr14 | 92167014 | ||||
chr14:92167014
|
C | CTTT | 9 | a0001c0001t0025a0001c0001t0029a0001c0001t0048others(6): Show | 14 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5283_*5285dupTTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5286 | INFO_REALIGN_3_PRIME | chr14 | 92167014 | ||||
chr14:92167014
|
C | CTTTT | 33 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(30): Show | 87 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*5282_*5285dupTTTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5286 | INFO_REALIGN_3_PRIME | chr14 | 92167014 | ||||
chr14:92167068
|
A | G | 142 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(139): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*5324A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5324 | chr14 | 92167068 | |||||
chr14:92167097
|
C | T | 1 | a0001c0001t0078 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5353C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5353 | chr14 | 92167097 | |||||
chr14:92167158
|
C | T | 1 | a0001c0001t0079 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5414C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5414 | chr14 | 92167158 | |||||
chr14:92167192
|
A | G | 1 | a0001c0001t0084 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5448A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5448 | chr14 | 92167192 | |||||
chr14:92167254
|
C | T | 1 | a0001c0001t0148 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5510C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5510 | chr14 | 92167254 | |||||
chr14:92167533
|
T | C | 1 | a0001c0001t0084 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5789T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5789 | chr14 | 92167533 | |||||
chr14:92167628
|
T | TA | 39 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(36): Show | 96 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*5884_*5885insA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5885 | chr14 | 92167628 | |||||
chr14:92167630
|
A | T | 39 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(36): Show | 96 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*5886A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5886 | chr14 | 92167630 | |||||
chr14:92167670
|
G | A | 142 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(139): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*5926G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5926 | chr14 | 92167670 | |||||
chr14:92167770
|
TTAATG | T | 33 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(30): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*6030_*6034delTGTA others(1): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6030 | INFO_REALIGN_3_PRIME | chr14 | 92167770 | ||||
chr14:92167797
|
G | C | 1 | a0001c0001t0040 | 2 | HG02258.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6053G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6053 | chr14 | 92167797 | |||||
chr14:92167844
|
G | A | 8 | a0001c0001t0042a0001c0001t0116a0001c0001t0117others(5): Show | 9 | HG02145.hp2 HG02922.hp1 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6100G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6100 | chr14 | 92167844 | |||||
chr14:92167850
|
A | G | 1 | a0001c0001t0068 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6106A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6106 | chr14 | 92167850 | |||||
chr14:92167889
|
C | T | 1 | a0001c0001t0107 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6145C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6145 | chr14 | 92167889 | |||||
chr14:92167892
|
G | GT | 31 | a0001c0001t0005a0001c0001t0006a0001c0001t0012others(28): Show | 77 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*6166dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6167 | INFO_REALIGN_3_PRIME | chr14 | 92167892 | ||||
chr14:92167892
|
G | GTT | 27 | a0001c0001t0001a0001c0001t0009a0001c0001t0022others(24): Show | 75 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*6165_*6166dupTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6167 | INFO_REALIGN_3_PRIME | chr14 | 92167892 | ||||
chr14:92167892
|
G | GTTT | 5 | a0001c0001t0008a0001c0001t0084a0001c0001t0087others(2): Show | 12 | HG02572.hp1 HG02976.hp1 HG03098.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6164_*6166dupTTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6167 | INFO_REALIGN_3_PRIME | chr14 | 92167892 | ||||
chr14:92167892
|
GT | G | 16 | a0001c0001t0014a0001c0001t0042a0001c0001t0050others(13): Show | 21 | HG00738.hp2 HG01109.hp2 HG02257.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*6166delT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6166 | INFO_REALIGN_3_PRIME | chr14 | 92167892 | ||||
chr14:92167892
|
GTT | G | 61 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(58): Show | 127 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*6165_*6166delTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6165 | INFO_REALIGN_3_PRIME | chr14 | 92167892 | ||||
chr14:92167898
|
T | G | 2 | a0001c0001t0144a0001c0001t0145 | 2 | HG00438.hp2 NA18953.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6154T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6154 | chr14 | 92167898 | |||||
chr14:92167900
|
T | G | 2 | a0001c0001t0014a0001c0001t0094 | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6156T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6156 | chr14 | 92167900 | |||||
chr14:92168061
|
A | G | 1 | a0001c0001t0040 | 2 | HG02258.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6317A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6317 | chr14 | 92168061 | |||||
chr14:92168078
|
C | T | 78 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(75): Show | 146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*6334C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6334 | chr14 | 92168078 | |||||
chr14:92168102
|
G | A | 1 | a0001c0001t0098 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6358G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6358 | chr14 | 92168102 | |||||
chr14:92168227
|
G | A | 2 | a0001c0001t0099a0001c0001t0100 | 2 | HG02486.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6483G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6483 | chr14 | 92168227 | |||||
chr14:92168229
|
C | T | 33 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(30): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*6485C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6485 | chr14 | 92168229 | |||||
chr14:92168248
|
C | CAAAAAAA | 6 | a0001c0001t0042a0001c0001t0113a0001c0001t0117others(3): Show | 7 | HG02809.hp2 HG02922.hp1 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6516_*6522dupAAAA others(3): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6523 | INFO_REALIGN_3_PRIME | chr14 | 92168248 | ||||
chr14:92168248
|
C | CAAAAAAA others(1): Show |
48 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(45): Show | 104 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*6515_*6522dupAAAA others(4): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6523 | INFO_REALIGN_3_PRIME | chr14 | 92168248 | ||||
chr14:92168248
|
C | CAAAAAAA others(2): Show |
19 | a0001c0001t0018a0001c0001t0019a0001c0001t0029others(16): Show | 30 | HG00423.hp2 HG00544.hp1 HG01517.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*6514_*6522dupAAAA others(5): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6523 | INFO_REALIGN_3_PRIME | chr14 | 92168248 | ||||
chr14:92168248
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0148 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6513_*6522dupAAAA others(6): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6523 | INFO_REALIGN_3_PRIME | chr14 | 92168248 | ||||
chr14:92168248
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0142 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6510_*6522dupAAAA others(9): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6523 | INFO_REALIGN_3_PRIME | chr14 | 92168248 | ||||
chr14:92168248
|
CA | C | 56 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(53): Show | 158 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*6522delA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6522 | INFO_REALIGN_3_PRIME | chr14 | 92168248 | ||||
chr14:92168350
|
T | A | 39 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(36): Show | 96 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*6606T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6606 | chr14 | 92168350 | |||||
chr14:92168413
|
A | T | 29 | a0001c0001t0005a0001c0001t0006a0001c0001t0012others(26): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*6669A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6669 | chr14 | 92168413 | |||||
chr14:92168523
|
C | T | 3 | a0001c0001t0025a0001c0001t0086a0001c0001t0087 | 5 | HG02055.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6779C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6779 | chr14 | 92168523 | |||||
chr14:92168577
|
A | G | 3 | a0001c0001t0025a0001c0001t0086a0001c0001t0087 | 5 | HG02055.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6833A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6833 | chr14 | 92168577 | |||||
chr14:92168627
|
C | T | 1 | a0001c0001t0147 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6883C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6883 | chr14 | 92168627 | |||||
chr14:92168744
|
A | G | 1 | a0001c0001t0071 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7000A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7000 | chr14 | 92168744 | |||||
chr14:92168799
|
G | A | 2 | a0001c0001t0023a0001c0001t0076 | 4 | HG02698.hp1 HG03239.hp2 HG04204.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7055G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7055 | chr14 | 92168799 | |||||
chr14:92168837
|
A | T | 1 | a0001c0001t0156 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7093A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7093 | chr14 | 92168837 | |||||
chr14:92168884
|
G | A | 1 | a0001c0001t0080 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7140G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7140 | chr14 | 92168884 | |||||
chr14:92169099
|
AAAG | A | 67 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(64): Show | 134 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*7359_*7361delAAG | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7359 | INFO_REALIGN_3_PRIME | chr14 | 92169099 | ||||
chr14:92169119
|
G | A | 1 | a0001c0001t0084 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7375G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7375 | chr14 | 92169119 | |||||
chr14:92169184
|
T | C | 1 | a0001c0001t0088 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7440T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7440 | chr14 | 92169184 | |||||
chr14:92169421
|
ATAAC | A | 32 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(29): Show | 90 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*7681_*7684delCTAA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7681 | INFO_REALIGN_3_PRIME | chr14 | 92169421 | ||||
chr14:92169527
|
A | T | 2 | a0001c0001t0057a0001c0001t0058 | 2 | NA18945.hp1 NA18954.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7783A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7783 | chr14 | 92169527 | |||||
chr14:92169629
|
T | C | 143 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(140): Show | 315 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*7885T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7885 | chr14 | 92169629 | |||||
chr14:92169631
|
A | G | 3 | a0001c0001t0061a0001c0001t0065a0001c0001t0067 | 3 | HG03491.hp1 HG03492.hp2 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7887A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7887 | chr14 | 92169631 | |||||
chr14:92169649
|
A | AT | 11 | a0001c0001t0055a0001c0001t0100a0001c0001t0105others(8): Show | 11 | HG00323.hp1 HG00735.hp1 HG01175.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7927dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7928 | INFO_REALIGN_3_PRIME | chr14 | 92169649 | ||||
chr14:92169649
|
AT | A | 13 | a0001c0001t0011a0001c0001t0014a0001c0001t0024others(10): Show | 22 | HG01071.hp2 HG01109.hp2 HG01515.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*7927delT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7927 | INFO_REALIGN_3_PRIME | chr14 | 92169649 | ||||
chr14:92169649
|
ATT | A | 52 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(49): Show | 143 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*7926_*7927delTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7926 | INFO_REALIGN_3_PRIME | chr14 | 92169649 | ||||
chr14:92169649
|
ATTT | A | 63 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(60): Show | 137 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*7925_*7927delTTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7925 | INFO_REALIGN_3_PRIME | chr14 | 92169649 | ||||
chr14:92169649
|
ATTTT | A | 7 | a0001c0001t0049a0001c0001t0057a0001c0001t0142others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG01361.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7924_*7927delTTTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7924 | INFO_REALIGN_3_PRIME | chr14 | 92169649 | ||||
chr14:92169810
|
A | C | 1 | a0001c0001t0064 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8066A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8066 | chr14 | 92169810 | |||||
chr14:92169885
|
C | T | 3 | a0001c0001t0114a0001c0001t0115a0001c0001t0122 | 3 | HG01884.hp1 HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8141C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8141 | chr14 | 92169885 | |||||
chr14:92169892
|
C | T | 1 | a0001c0001t0075 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8148C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8148 | chr14 | 92169892 | |||||
chr14:92169972
|
T | A | 1 | a0001c0001t0023 | 3 | HG02698.hp1 HG03239.hp2 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8228T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8228 | chr14 | 92169972 | |||||
chr14:92170077
|
G | A | 39 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(36): Show | 96 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*8333G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8333 | chr14 | 92170077 | |||||
chr14:92170084
|
A | G | 1 | a0001c0001t0131 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8340A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8340 | chr14 | 92170084 | |||||
chr14:92170089
|
G | A | 11 | a0001c0001t0042a0001c0001t0114a0001c0001t0115others(8): Show | 12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*8345G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8345 | chr14 | 92170089 | |||||
chr14:92170097
|
A | T | 6 | a0001c0001t0116a0001c0001t0117a0001c0001t0118others(3): Show | 6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8353A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8353 | chr14 | 92170097 | |||||
chr14:92170332
|
T | G | 78 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(75): Show | 146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*8588T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8588 | chr14 | 92170332 | |||||
chr14:92170369
|
A | T | 62 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(59): Show | 163 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*8625A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8625 | chr14 | 92170369 | |||||
chr14:92170590
|
C | G | 30 | a0001c0001t0005a0001c0001t0006a0001c0001t0012others(27): Show | 73 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*8846C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8846 | chr14 | 92170590 | |||||
chr14:92170739
|
G | A | 27 | a0001c0001t0020a0001c0001t0021a0001c0001t0031others(24): Show | 37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*8995G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8995 | chr14 | 92170739 | |||||
chr14:92170759
|
A | G | 1 | a0001c0001t0104 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9015A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9015 | chr14 | 92170759 | |||||
chr14:92170802
|
G | C | 1 | a0001c0001t0102 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9058G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9058 | chr14 | 92170802 | |||||
chr14:92170899
|
C | T | 78 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(75): Show | 146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*9155C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9155 | chr14 | 92170899 | |||||
chr14:92171006
|
G | A | 3 | a0001c0001t0014a0001c0001t0094a0001c0001t0151 | 6 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9262G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9262 | chr14 | 92171006 | |||||
chr14:92171164
|
T | C | 1 | a0001c0001t0152 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9420T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9420 | chr14 | 92171164 | |||||
chr14:92171167
|
C | T | 1 | a0001c0001t0152 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9423C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9423 | chr14 | 92171167 | |||||
chr14:92171203
|
T | A | 1 | a0001c0001t0085 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9459T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9459 | chr14 | 92171203 | |||||
chr14:92171234
|
T | C | 143 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(140): Show | 315 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*9490T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9490 | chr14 | 92171234 | |||||
chr14:92171342
|
T | C | 1 | a0001c0001t0113 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9598T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9598 | chr14 | 92171342 | |||||
chr14:92171443
|
T | C | 1 | a0001c0001t0103 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9699T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9699 | chr14 | 92171443 | |||||
chr14:92171556
|
T | C | 27 | a0001c0001t0020a0001c0001t0021a0001c0001t0031others(24): Show | 37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*9812T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9812 | chr14 | 92171556 | |||||
chr14:92171624
|
C | T | 1 | a0001c0001t0127 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9880C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9880 | chr14 | 92171624 | |||||
chr14:92171625
|
G | A | 1 | a0001c0001t0134 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9881G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9881 | chr14 | 92171625 | |||||
chr14:92171675
|
G | A | 1 | a0001c0001t0144 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9931G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9931 | chr14 | 92171675 | |||||
chr14:92171703
|
T | C | 1 | a0001c0001t0064 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9959T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9959 | chr14 | 92171703 | |||||
chr14:92171708
|
G | A | 4 | a0001c0001t0025a0001c0001t0086a0001c0001t0087others(1): Show | 6 | HG02055.hp1 HG02451.hp1 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9964G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9964 | chr14 | 92171708 | |||||
chr14:92172041
|
G | T | 1 | a0001c0001t0129 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10297G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 10297 | chr14 | 92172041 | |||||
chr14:92172098
|
A | G | 33 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(30): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*10354A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 10354 | chr14 | 92172098 | |||||
chr14:92172124
|
A | G | 143 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(140): Show | 315 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*10380A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 10380 | chr14 | 92172124 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:92122151
|
A | G | 1 | a0001c0001t0003g0262 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-94+23A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122151 | ||||||
chr14:92122250
|
C | T | 1 | a0001c0001t0118g0261 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-94+122C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122250 | ||||||
chr14:92122266
|
G | T | 1 | a0001c0001t0003g0262 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-94+138G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122266 | ||||||
chr14:92122330
|
C | G | 13 | a0001c0001t0042g0252a0001c0001t0042g0257a0001c0001t0113g0253others(10): Show | 13 | HG01884.hp1 HG02145.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.-94+202C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122330 | ||||||
chr14:92122344
|
G | A | 88 | a0001c0001t0001g0110a0001c0001t0003g0009a0001c0001t0003g0010others(85): Show | 89 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-94+216G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122344 | ||||||
chr14:92122383
|
C | T | 1 | a0001c0001t0028g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-94+255C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122383 | ||||||
chr14:92122467
|
G | C | 34 | a0001c0001t0012g0130a0001c0001t0016g0131a0001c0001t0016g0132others(31): Show | 39 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(36): Show |
intron_variant | MODIFIER | c.-94+339G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122467 | ||||||
chr14:92122573
|
T | A | 220 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 240 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.-94+445T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122573 | ||||||
chr14:92122644
|
C | T | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-94+516C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122644 | ||||||
chr14:92122654
|
C | T | 5 | a0001c0001t0003g0262a0001c0001t0010g0114a0001c0001t0019g0112others(2): Show | 5 | HG01081.hp1 HG02683.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-94+526C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122654 | ||||||
chr14:92122677
|
C | A | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-94+549C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122677 | ||||||
chr14:92122708
|
A | AT | 78 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(75): Show | 92 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.-94+584dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 92122708 | |||||
chr14:92122763
|
T | C | 220 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 240 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.-94+635T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122763 | ||||||
chr14:92122853
|
C | CT | 90 | a0001c0001t0001g0184a0001c0001t0003g0009a0001c0001t0003g0010others(87): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.-94+740dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 92122853 | |||||
chr14:92122853
|
C | CTT | 6 | a0001c0001t0003g0107a0001c0001t0003g0109a0001c0001t0004g0108others(3): Show | 6 | HG00673.hp2 HG01433.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.-94+739_-94+740dup others(2): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 92122853 | |||||
chr14:92122868
|
T | A | 1 | a0001c0001t0042g0252 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-94+740T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122868 | ||||||
chr14:92122868
|
T | TA | 12 | a0001c0001t0042g0257a0001c0001t0113g0253a0001c0001t0114g0254others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.-94+742dupA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 92122868 | |||||
chr14:92123004
|
G | A | 53 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(50): Show | 68 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.-94+876G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123004 | ||||||
chr14:92123093
|
G | T | 1 | a0001c0001t0052g0039 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-94+965G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123093 | ||||||
chr14:92123149
|
A | G | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-94+1021A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123149 | ||||||
chr14:92123156
|
C | G | 2 | a0001c0001t0034g0105a0001c0001t0157g0106 | 2 | NA18984.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-94+1028C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123156 | ||||||
chr14:92123197
|
C | T | 1 | a0001c0001t0005g0219 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-94+1069C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123197 | ||||||
chr14:92123384
|
G | T | 54 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(51): Show | 69 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-94+1256G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123384 | ||||||
chr14:92123414
|
T | C | 6 | a0001c0001t0034g0031a0001c0001t0035g0016a0001c0001t0036g0016others(3): Show | 7 | NA18950.hp2 NA18980.hp1 NA18997.hp1 others(4): Show |
intron_variant | MODIFIER | c.-94+1286T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123414 | ||||||
chr14:92123421
|
C | T | 12 | a0001c0001t0042g0252a0001c0001t0042g0257a0001c0001t0114g0254others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.-94+1293C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123421 | ||||||
chr14:92123598
|
CAT | C | 34 | a0001c0001t0012g0130a0001c0001t0016g0131a0001c0001t0016g0132others(31): Show | 39 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(36): Show |
intron_variant | MODIFIER | c.-94+1473_-94+1474d others(4): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 92123598 | |||||
chr14:92123776
|
C | T | 142 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(139): Show | 148 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.-94+1648C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123776 | ||||||
chr14:92123848
|
A | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(75): Show | 92 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.-94+1720A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123848 | ||||||
chr14:92123866
|
A | G | 1 | a0001c0001t0011g0244 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-94+1738A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123866 | ||||||
chr14:92123922
|
T | A | 2 | a0001c0001t0001g0141a0001c0001t0038g0142 | 2 | NA18962.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-94+1794T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123922 | ||||||
chr14:92124220
|
T | A | 220 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 240 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.-93-1902T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92124220 | ||||||
chr14:92124278
|
T | C | 10 | a0001c0001t0005g0018a0001c0001t0006g0014a0001c0001t0006g0018others(7): Show | 12 | HG00621.hp1 HG02015.hp2 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.-93-1844T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92124278 | ||||||
chr14:92124495
|
T | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(75): Show | 92 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.-93-1627T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92124495 | ||||||
chr14:92124513
|
G | A | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-1609G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92124513 | ||||||
chr14:92124809
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-93-1313A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92124809 | ||||||
chr14:92124948
|
G | A | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-1174G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92124948 | ||||||
chr14:92125049
|
T | G | 1 | a0001c0001t0009g0143 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-93-1073T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92125049 | ||||||
chr14:92125196
|
A | T | 53 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(50): Show | 68 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.-93-926A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92125196 | ||||||
chr14:92125499
|
A | G | 2 | a0001c0001t0004g0104a0001c0001t0100g0243 | 2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-93-623A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92125499 | ||||||
chr14:92125634
|
C | G | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 90 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.-93-488C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92125634 | ||||||
chr14:92125823
|
A | G | 1 | a0001c0001t0004g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-93-299A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92125823 | ||||||
chr14:92125868
|
T | C | 1 | a0001c0001t0004g0053 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-93-254T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92125868 | ||||||
chr14:92125925
|
TTA | T | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-195_-93-194del others(2): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 92125925 | |||||
chr14:92125966
|
A | G | 1 | a0001c0001t0005g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-93-156A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92125966 | ||||||
chr14:92125987
|
T | G | 3 | a0001c0001t0114g0254a0001c0001t0115g0255a0001c0001t0122g0256 | 3 | HG01884.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-93-135T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92125987 | ||||||
chr14:92126033
|
C | G | 1 | a0001c0001t0097g0241 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-93-89C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92126033 | ||||||
chr14:92126047
|
A | G | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.-93-75A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92126047 | ||||||
chr14:92126312
|
A | G | 1 | a0001c0001t0097g0241 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-35+132A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92126312 | ||||||
chr14:92126414
|
A | G | 134 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 163 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.-35+234A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92126414 | ||||||
chr14:92126598
|
C | T | 6 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(3): Show | 6 | HG01255.hp2 HG03041.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+418C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92126598 | ||||||
chr14:92126673
|
C | T | 1 | a0001c0001t0120g0260 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-35+493C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92126673 | ||||||
chr14:92126679
|
C | T | 2 | a0001c0001t0090g0178a0001c0001t0166g0103 | 2 | HG01168.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-35+499C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92126679 | ||||||
chr14:92126811
|
A | G | 5 | a0001c0001t0025g0037a0001c0001t0025g0175a0001c0001t0025g0176others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+631A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92126811 | ||||||
chr14:92127142
|
A | T | 1 | a0001c0001t0080g0174 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-35+962A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92127142 | ||||||
chr14:92127301
|
A | G | 1 | a0001c0001t0008g0173 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-35+1121A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92127301 | ||||||
chr14:92127437
|
C | T | 1 | a0001c0001t0084g0172 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-35+1257C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92127437 | ||||||
chr14:92127449
|
T | G | 1 | a0001c0001t0033g0117 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-35+1269T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92127449 | ||||||
chr14:92127525
|
A | G | 1 | a0001c0001t0113g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-35+1345A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92127525 | ||||||
chr14:92127526
|
T | C | 1 | a0001c0001t0123g0191 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-35+1346T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92127526 | ||||||
chr14:92127666
|
A | G | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+1486A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92127666 | ||||||
chr14:92127869
|
T | A | 1 | a0001c0001t0011g0244 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-35+1689T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92127869 | ||||||
chr14:92127993
|
C | T | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
intron_variant | MODIFIER | c.-35+1813C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92127993 | ||||||
chr14:92128036
|
C | G | 10 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0099others(7): Show | 10 | HG02083.hp1 NA18952.hp2 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35+1856C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92128036 | ||||||
chr14:92128040
|
C | T | 1 | a0001c0001t0113g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-35+1860C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92128040 | ||||||
chr14:92128235
|
C | CA | 140 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(137): Show | 146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.-35+2065dupA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 92128235 | |||||
chr14:92128343
|
C | T | 1 | a0001c0001t0113g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-35+2163C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92128343 | ||||||
chr14:92128541
|
T | C | 140 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(137): Show | 146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.-35+2361T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92128541 | ||||||
chr14:92128900
|
A | G | 2 | a0001c0001t0029g0140a0001c0001t0141g0139 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-34-2051A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92128900 | ||||||
chr14:92128935
|
G | T | 1 | a0001c0001t0002g0051 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-34-2016G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92128935 | ||||||
chr14:92128954
|
A | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG00544.hp2 NA18612.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-34-1997A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92128954 | ||||||
chr14:92128961
|
A | G | 1 | a0001c0001t0082g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-34-1990A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92128961 | ||||||
chr14:92129059
|
A | G | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-1892A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129059 | ||||||
chr14:92129060
|
T | A | 1 | a0001c0001t0142g0054 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-34-1891T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129060 | ||||||
chr14:92129135
|
G | A | 6 | a0001c0001t0006g0007a0001c0001t0016g0193a0001c0001t0017g0007others(3): Show | 8 | HG02615.hp2 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34-1816G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129135 | ||||||
chr14:92129137
|
A | T | 12 | a0001c0001t0042g0252a0001c0001t0042g0257a0001c0001t0114g0254others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.-34-1814A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129137 | ||||||
chr14:92129533
|
T | G | 1 | a0001c0001t0133g0192 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-34-1418T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129533 | ||||||
chr14:92129543
|
C | T | 5 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(2): Show | 5 | HG01255.hp2 HG03041.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-1408C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129543 | ||||||
chr14:92129550
|
C | G | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-1401C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129550 | ||||||
chr14:92129555
|
C | T | 1 | a0001c0001t0006g0217 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-34-1396C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129555 | ||||||
chr14:92129567
|
T | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 9 | NA18951.hp1 NA18960.hp2 NA18977.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34-1384T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129567 | ||||||
chr14:92129649
|
T | C | 1 | a0001c0001t0063g0118 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-34-1302T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129649 | ||||||
chr14:92129660
|
C | T | 10 | a0001c0001t0003g0052a0001c0001t0004g0015a0001c0001t0004g0027others(7): Show | 11 | HG00558.hp1 HG00609.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.-34-1291C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129660 | ||||||
chr14:92129809
|
G | A | 1 | a0001c0001t0008g0148 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-34-1142G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129809 | ||||||
chr14:92129813
|
T | C | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.-34-1138T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129813 | ||||||
chr14:92129917
|
T | C | 1 | a0001c0001t0009g0149 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-34-1034T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129917 | ||||||
chr14:92130129
|
C | T | 6 | a0001c0001t0116g0023a0001c0001t0117g0023a0001c0001t0118g0261others(3): Show | 6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34-822C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130129 | ||||||
chr14:92130130
|
G | A | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-821G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130130 | ||||||
chr14:92130223
|
C | A | 1 | a0001c0001t0001g0184 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-34-728C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130223 | ||||||
chr14:92130465
|
A | G | 62 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 74 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-34-486A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130465 | ||||||
chr14:92130532
|
T | C | 3 | a0001c0001t0042g0252a0001c0001t0042g0257a0001c0001t0121g0258 | 3 | HG02145.hp2 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-34-419T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130532 | ||||||
chr14:92130548
|
A | G | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-403A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130548 | ||||||
chr14:92130678
|
G | A | 1 | a0001c0001t0003g0055 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-34-273G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130678 | ||||||
chr14:92130748
|
A | T | 2 | a0001c0001t0030g0239a0001c0001t0030g0240 | 2 | HG01069.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-34-203A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130748 | ||||||
chr14:92130806
|
A | G | 1 | a0001c0001t0013g0216 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-34-145A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130806 | ||||||
chr14:92130884
|
C | A | 134 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 163 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.-34-67C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130884 | ||||||
chr14:92130885
|
A | C | 1 | a0001c0001t0001g0168 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-34-66A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130885 | ||||||
chr14:92131203
|
C | T | 1 | a0001c0001t0113g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.149+70C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131203 | ||||||
chr14:92131246
|
G | A | 1 | a0001c0001t0138g0195 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.149+113G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131246 | ||||||
chr14:92131548
|
T | C | 1 | a0001c0001t0008g0155 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.149+415T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131548 | ||||||
chr14:92131695
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0167a0001c0001t0024g0017others(1): Show | 4 | NA18972.hp2 NA18995.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+562C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131695 | ||||||
chr14:92131811
|
C | T | 2 | a0001c0001t0003g0026a0001c0001t0047g0026 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.149+678C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131811 | ||||||
chr14:92131847
|
AT | A | 5 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0049g0090others(2): Show | 5 | HG01069.hp1 NA18747.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+715delT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131847 | ||||||
chr14:92131848
|
T | A | 90 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(87): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.149+715T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131848 | ||||||
chr14:92131851
|
G | A | 95 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(92): Show | 96 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.149+718G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131851 | ||||||
chr14:92131853
|
T | A | 1 | a0001c0001t0150g0091 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.149+720T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131853 | ||||||
chr14:92131915
|
A | G | 140 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(137): Show | 146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.149+782A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131915 | ||||||
chr14:92131955
|
C | A | 1 | a0001c0001t0097g0241 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.149+822C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131955 | ||||||
chr14:92131977
|
T | C | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
intron_variant | MODIFIER | c.149+844T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131977 | ||||||
chr14:92132065
|
C | T | 1 | a0001c0001t0113g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.149+932C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132065 | ||||||
chr14:92132280
|
A | G | 1 | a0001c0001t0129g0215 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.149+1147A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132280 | ||||||
chr14:92132291
|
G | T | 140 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(137): Show | 146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.149+1158G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132291 | ||||||
chr14:92132469
|
G | C | 1 | a0001c0001t0067g0119 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.149+1336G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132469 | ||||||
chr14:92132517
|
A | G | 1 | a0001c0001t0037g0129 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.149+1384A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132517 | ||||||
chr14:92132526
|
C | T | 31 | a0001c0001t0020g0011a0001c0001t0021g0004a0001c0001t0021g0126others(28): Show | 36 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(33): Show |
intron_variant | MODIFIER | c.149+1393C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132526 | ||||||
chr14:92132543
|
G | A | 1 | a0001c0001t0124g0245 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.149+1410G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132543 | ||||||
chr14:92132569
|
C | T | 1 | a0001c0001t0125g0190 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.149+1436C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132569 | ||||||
chr14:92132621
|
G | A | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
intron_variant | MODIFIER | c.150-1390G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132621 | ||||||
chr14:92132703
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.150-1308C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132703 | ||||||
chr14:92132767
|
C | T | 1 | a0001c0001t0008g0173 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.150-1244C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132767 | ||||||
chr14:92132791
|
A | C | 1 | a0001c0001t0076g0166 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.150-1220A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132791 | ||||||
chr14:92133029
|
G | A | 31 | a0001c0001t0020g0011a0001c0001t0021g0004a0001c0001t0021g0126others(28): Show | 36 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(33): Show |
intron_variant | MODIFIER | c.150-982G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133029 | ||||||
chr14:92133076
|
C | T | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-935C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133076 | ||||||
chr14:92133137
|
T | C | 280 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(277): Show | 315 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(312): Show |
intron_variant | MODIFIER | c.150-874T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133137 | ||||||
chr14:92133139
|
G | T | 1 | a0001c0001t0113g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.150-872G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133139 | ||||||
chr14:92133144
|
G | A | 1 | a0001c0001t0046g0111 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.150-867G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133144 | ||||||
chr14:92133180
|
G | A | 1 | a0001c0001t0146g0056 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.150-831G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133180 | ||||||
chr14:92133186
|
G | A | 5 | a0001c0001t0003g0057a0001c0001t0003g0058a0001c0001t0003g0059others(2): Show | 5 | NA18954.hp1 NA18966.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-825G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133186 | ||||||
chr14:92133220
|
GACCACCC others(15): Show |
G | 1 | a0001c0001t0066g0115 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.150-789_150-768del others(22): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 92133220 | |||||
chr14:92133235
|
C | G | 1 | a0001c0001t0001g0110 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.150-776C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133235 | ||||||
chr14:92133267
|
A | G | 1 | a0001c0001t0010g0114 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.150-744A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133267 | ||||||
chr14:92133291
|
T | C | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-720T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133291 | ||||||
chr14:92133343
|
T | C | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
intron_variant | MODIFIER | c.150-668T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133343 | ||||||
chr14:92133361
|
G | A | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-650G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133361 | ||||||
chr14:92133442
|
T | TGTG | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
intron_variant | MODIFIER | c.150-568_150-566dup others(3): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 92133442 | |||||
chr14:92133517
|
A | G | 96 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(93): Show | 97 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.150-494A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133517 | ||||||
chr14:92133529
|
T | C | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.150-482T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133529 | ||||||
chr14:92133622
|
C | CT | 102 | a0001c0001t0001g0147a0001c0001t0001g0183a0001c0001t0003g0009others(99): Show | 103 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.150-375dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 92133622 | |||||
chr14:92133646
|
A | G | 1 | a0001c0001t0113g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.150-365A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133646 | ||||||
chr14:92133652
|
A | G | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.150-359A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133652 | ||||||
chr14:92133833
|
G | A | 5 | a0001c0001t0002g0043a0001c0001t0002g0220a0001c0001t0002g0221others(2): Show | 5 | HG00099.hp2 HG00738.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-178G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133833 | ||||||
chr14:92134212
|
G | A | 2 | a0001c0001t0026g0150a0001c0001t0026g0151 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.310-38G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 4/15 | chr14 | 92134212 | ||||||
chr14:92134441
|
A | G | 56 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(53): Show | 71 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.415+86A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92134441 | ||||||
chr14:92134454
|
G | T | 145 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(142): Show | 151 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.415+99G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92134454 | ||||||
chr14:92134563
|
G | A | 1 | a0001c0001t0002g0222 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.415+208G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92134563 | ||||||
chr14:92134614
|
A | G | 12 | a0001c0001t0042g0252a0001c0001t0042g0257a0001c0001t0114g0254others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+259A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92134614 | ||||||
chr14:92134674
|
A | T | 2 | a0001c0001t0053g0213a0001c0001t0054g0214 | 2 | HG00558.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.415+319A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92134674 | ||||||
chr14:92134761
|
G | A | 1 | a0001c0001t0013g0186 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.415+406G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92134761 | ||||||
chr14:92134837
|
A | G | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.415+482A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92134837 | ||||||
chr14:92134862
|
C | G | 140 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(137): Show | 146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.416-505C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92134862 | ||||||
chr14:92134942
|
A | C | 1 | a0001c0001t0004g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.416-425A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92134942 | ||||||
chr14:92135050
|
A | G | 12 | a0001c0001t0042g0252a0001c0001t0042g0257a0001c0001t0114g0254others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-317A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92135050 | ||||||
chr14:92135536
|
GTAT | G | 12 | a0001c0001t0042g0252a0001c0001t0042g0257a0001c0001t0114g0254others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.545+45_545+47delAT others(1): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 92135536 | |||||
chr14:92135625
|
G | A | 1 | a0001c0001t0090g0178 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.545+129G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92135625 | ||||||
chr14:92135730
|
G | A | 3 | a0001c0001t0026g0150a0001c0001t0026g0151a0001c0001t0093g0152 | 3 | HG02486.hp2 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.545+234G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92135730 | ||||||
chr14:92135884
|
T | C | 1 | a0001c0001t0084g0172 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.545+388T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92135884 | ||||||
chr14:92135885
|
A | G | 145 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(142): Show | 151 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.545+389A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92135885 | ||||||
chr14:92136182
|
G | A | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.545+686G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92136182 | ||||||
chr14:92136543
|
T | C | 140 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(137): Show | 146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.545+1047T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92136543 | ||||||
chr14:92136618
|
G | A | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.545+1122G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92136618 | ||||||
chr14:92136630
|
A | G | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
intron_variant | MODIFIER | c.545+1134A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92136630 | ||||||
chr14:92136753
|
G | A | 2 | a0001c0001t0045g0196a0001c0001t0045g0197 | 2 | HG01346.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.545+1257G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92136753 | ||||||
chr14:92136883
|
T | C | 1 | a0001c0001t0016g0198 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.546-1349T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92136883 | ||||||
chr14:92136931
|
T | A | 1 | a0001c0001t0090g0178 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.546-1301T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92136931 | ||||||
chr14:92136967
|
T | G | 329 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(326): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.546-1265T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92136967 | ||||||
chr14:92137020
|
T | TA | 140 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(137): Show | 146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.546-1201dupA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 92137020 | |||||
chr14:92137050
|
TGCA | T | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.546-1178_546-1176d others(5): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 92137050 | |||||
chr14:92137122
|
G | C | 1 | a0001c0001t0001g0169 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.546-1110G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92137122 | ||||||
chr14:92137232
|
T | C | 1 | a0001c0001t0118g0261 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.546-1000T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92137232 | ||||||
chr14:92137294
|
C | T | 31 | a0001c0001t0020g0011a0001c0001t0021g0004a0001c0001t0021g0126others(28): Show | 36 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(33): Show |
intron_variant | MODIFIER | c.546-938C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92137294 | ||||||
chr14:92137320
|
C | T | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.546-912C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92137320 | ||||||
chr14:92137919
|
G | C | 1 | a0001c0001t0063g0118 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.546-313G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92137919 | ||||||
chr14:92138138
|
T | G | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.546-94T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92138138 | ||||||
chr14:92138361
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG00544.hp2 HG02135.hp2 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.661+14C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92138361 | ||||||
chr14:92138580
|
C | A | 1 | a0001c0001t0118g0261 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.661+233C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92138580 | ||||||
chr14:92138799
|
A | G | 31 | a0001c0001t0020g0011a0001c0001t0021g0004a0001c0001t0021g0126others(28): Show | 36 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(33): Show |
intron_variant | MODIFIER | c.661+452A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92138799 | ||||||
chr14:92138897
|
T | TG | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.661+552dupG | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92138897 | |||||
chr14:92138950
|
C | T | 1 | a0001c0001t0113g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.661+603C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92138950 | ||||||
chr14:92139037
|
C | T | 1 | a0001c0001t0016g0198 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.661+690C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139037 | ||||||
chr14:92139056
|
C | T | 1 | a0001c0001t0048g0137 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.661+709C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139056 | ||||||
chr14:92139095
|
G | A | 1 | a0001c0001t0047g0092 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.661+748G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139095 | ||||||
chr14:92139169
|
C | G | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
intron_variant | MODIFIER | c.661+822C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139169 | ||||||
chr14:92139234
|
G | A | 3 | a0001c0001t0003g0262a0001c0001t0019g0112a0001c0001t0046g0111 | 3 | HG02683.hp1 HG02735.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.661+887G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139234 | ||||||
chr14:92139244
|
C | T | 1 | a0001c0001t0013g0212 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.661+897C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139244 | ||||||
chr14:92139342
|
G | A | 1 | a0001c0001t0124g0245 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.661+995G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139342 | ||||||
chr14:92139403
|
T | C | 248 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(245): Show | 278 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(275): Show |
intron_variant | MODIFIER | c.661+1056T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139403 | ||||||
chr14:92139411
|
C | T | 140 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(137): Show | 146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.661+1064C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139411 | ||||||
chr14:92139463
|
C | G | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
intron_variant | MODIFIER | c.661+1116C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139463 | ||||||
chr14:92139465
|
G | A | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
intron_variant | MODIFIER | c.661+1118G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139465 | ||||||
chr14:92139534
|
A | G | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.661+1187A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139534 | ||||||
chr14:92139539
|
C | CT | 18 | a0001c0001t0001g0167a0001c0001t0003g0057a0001c0001t0006g0211others(15): Show | 20 | HG00140.hp2 HG00408.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.661+1209dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92139539 | |||||
chr14:92139539
|
CT | C | 12 | a0001c0001t0042g0252a0001c0001t0042g0257a0001c0001t0114g0254others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.661+1209delT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92139539 | |||||
chr14:92139592
|
G | A | 1 | a0001c0001t0013g0212 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.661+1245G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139592 | ||||||
chr14:92139735
|
C | T | 34 | a0001c0001t0020g0011a0001c0001t0021g0004a0001c0001t0021g0126others(31): Show | 39 | HG00408.hp2 HG01884.hp1 HG02040.hp2 others(36): Show |
intron_variant | MODIFIER | c.661+1388C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139735 | ||||||
chr14:92139741
|
G | A | 96 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(93): Show | 97 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.661+1394G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139741 | ||||||
chr14:92139786
|
G | A | 1 | a0001c0001t0113g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.661+1439G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139786 | ||||||
chr14:92139787
|
C | A | 1 | a0001c0001t0113g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.661+1440C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139787 | ||||||
chr14:92139821
|
A | G | 1 | a0001c0001t0019g0086 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.661+1474A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139821 | ||||||
chr14:92139846
|
C | A | 1 | a0001c0001t0002g0223 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.661+1499C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139846 | ||||||
chr14:92139948
|
C | CT | 8 | a0001c0001t0012g0019a0001c0001t0012g0130a0001c0001t0013g0188others(5): Show | 9 | HG01975.hp1 HG02055.hp2 HG04184.hp1 others(6): Show |
intron_variant | MODIFIER | c.661+1602dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92139948 | |||||
chr14:92139949
|
TA | T | 3 | a0001c0001t0005g0040a0001c0001t0013g0040a0001c0001t0131g0187 | 3 | HG03942.hp1 NA18959.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.661+1603delA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139949 | ||||||
chr14:92139950
|
A | AT | 99 | a0001c0001t0001g0147a0001c0001t0001g0179a0001c0001t0002g0021others(96): Show | 102 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.661+1625dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92139950 | |||||
chr14:92139950
|
A | ATT | 104 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 123 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.661+1624_661+1625d others(4): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92139950 | |||||
chr14:92139950
|
A | ATTT | 8 | a0001c0001t0001g0164a0001c0001t0001g0183a0001c0001t0001g0184others(5): Show | 8 | HG02145.hp2 HG02683.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.661+1623_661+1625d others(5): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92139950 | |||||
chr14:92139950
|
A | T | 54 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0041others(51): Show | 69 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.661+1603A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139950 | ||||||
chr14:92140042
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.661+1695C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140042 | ||||||
chr14:92140103
|
G | T | 1 | a0001c0001t0002g0221 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.661+1756G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140103 | ||||||
chr14:92140143
|
G | T | 4 | a0001c0001t0026g0150a0001c0001t0026g0151a0001c0001t0026g0153others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.661+1796G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140143 | ||||||
chr14:92140193
|
C | G | 3 | a0001c0001t0014g0248a0001c0001t0014g0249a0001c0001t0014g0250 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.661+1846C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140193 | ||||||
chr14:92140194
|
C | T | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.661+1847C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140194 | ||||||
chr14:92140241
|
C | T | 12 | a0001c0001t0042g0252a0001c0001t0042g0257a0001c0001t0114g0254others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.661+1894C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140241 | ||||||
chr14:92140399
|
A | G | 1 | a0001c0001t0027g0234 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.662-1765A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140399 | ||||||
chr14:92140424
|
A | AC | 5 | a0001c0001t0015g0048a0001c0001t0041g0048a0001c0001t0107g0233others(2): Show | 5 | HG02055.hp2 HG03239.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.662-1735dupC | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92140424 | |||||
chr14:92140434
|
C | CT | 183 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(180): Show | 204 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.662-1713dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92140434 | |||||
chr14:92140434
|
C | CTT | 11 | a0001c0001t0006g0211a0001c0001t0042g0252a0001c0001t0042g0257others(8): Show | 11 | HG00438.hp2 HG02145.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.662-1714_662-1713d others(4): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92140434 | |||||
chr14:92140494
|
G | A | 1 | a0001c0001t0112g0232 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.662-1670G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140494 | ||||||
chr14:92140530
|
T | C | 31 | a0001c0001t0020g0011a0001c0001t0021g0004a0001c0001t0021g0126others(28): Show | 36 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(33): Show |
intron_variant | MODIFIER | c.662-1634T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140530 | ||||||
chr14:92140557
|
C | T | 4 | a0001c0001t0026g0150a0001c0001t0026g0151a0001c0001t0026g0153others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-1607C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140557 | ||||||
chr14:92140654
|
G | A | 56 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(53): Show | 68 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.662-1510G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140654 | ||||||
chr14:92140657
|
C | T | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.662-1507C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140657 | ||||||
chr14:92140686
|
C | A | 1 | a0001c0001t0002g0220 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.662-1478C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140686 | ||||||
chr14:92140703
|
A | AT | 96 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(93): Show | 97 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.662-1459dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92140703 | |||||
chr14:92140747
|
A | G | 1 | a0001c0001t0102g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.662-1417A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140747 | ||||||
chr14:92140806
|
T | A | 1 | a0001c0001t0077g0156 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.662-1358T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140806 | ||||||
chr14:92140941
|
A | G | 1 | a0001c0001t0009g0143 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.662-1223A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140941 | ||||||
chr14:92141040
|
A | G | 1 | a0001c0001t0028g0231 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.662-1124A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92141040 | ||||||
chr14:92141086
|
A | T | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.662-1078A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92141086 | ||||||
chr14:92141230
|
A | T | 12 | a0001c0001t0042g0252a0001c0001t0042g0257a0001c0001t0114g0254others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.662-934A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92141230 | ||||||
chr14:92141488
|
C | T | 1 | a0001c0001t0005g0200 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.662-676C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92141488 | ||||||
chr14:92141522
|
C | T | 1 | a0001c0001t0113g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.662-642C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92141522 | ||||||
chr14:92142052
|
G | A | 1 | a0001c0001t0004g0061 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.662-112G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92142052 | ||||||
chr14:92142135
|
T | C | 1 | a0001c0001t0010g0097 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.662-29T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92142135 | ||||||
chr14:92142563
|
C | G | 31 | a0001c0001t0020g0011a0001c0001t0021g0004a0001c0001t0021g0126others(28): Show | 36 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(33): Show |
intron_variant | MODIFIER | c.849+212C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 8/15 | chr14 | 92142563 | ||||||
chr14:92142577
|
T | A | 1 | a0001c0001t0027g0236 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.849+226T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 8/15 | chr14 | 92142577 | ||||||
chr14:92142990
|
T | C | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.850-14T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 8/15 | chr14 | 92142990 | ||||||
chr14:92143358
|
A | G | 1 | a0001c0001t0094g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1140+64A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92143358 | ||||||
chr14:92143486
|
C | A | 1 | a0001c0001t0006g0217 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1140+192C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92143486 | ||||||
chr14:92143486
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1140+192C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92143486 | ||||||
chr14:92143544
|
T | TA | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1140+259dupA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92143544 | |||||
chr14:92143665
|
G | T | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1140+371G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92143665 | ||||||
chr14:92143766
|
TG | T | 62 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(59): Show | 77 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1140+474delG | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92143766 | |||||
chr14:92143799
|
CGTT | C | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1140+508_1140+510d others(5): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92143799 | |||||
chr14:92143869
|
T | C | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1140+575T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92143869 | ||||||
chr14:92143879
|
C | G | 1 | a0001c0001t0014g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1140+585C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92143879 | ||||||
chr14:92143987
|
C | T | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1140+693C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92143987 | ||||||
chr14:92144044
|
G | A | 1 | a0001c0001t0018g0062 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1140+750G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92144044 | ||||||
chr14:92144082
|
T | C | 5 | a0001c0001t0003g0262a0001c0001t0010g0114a0001c0001t0019g0112others(2): Show | 5 | HG01081.hp1 HG02683.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1140+788T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92144082 | ||||||
chr14:92144086
|
C | T | 1 | a0001c0001t0146g0056 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1140+792C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92144086 | ||||||
chr14:92144259
|
T | A | 134 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 163 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.1140+965T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92144259 | ||||||
chr14:92144598
|
T | G | 1 | a0001c0001t0008g0173 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1140+1304T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92144598 | ||||||
chr14:92144717
|
A | G | 5 | a0001c0001t0002g0050a0001c0001t0002g0229a0001c0001t0002g0230others(2): Show | 6 | HG01081.hp2 HG01891.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1140+1423A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92144717 | ||||||
chr14:92144732
|
C | A | 1 | a0001c0001t0113g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1140+1438C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92144732 | ||||||
chr14:92144742
|
G | C | 1 | a0001c0001t0010g0063 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1140+1448G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92144742 | ||||||
chr14:92144887
|
A | G | 12 | a0001c0001t0042g0252a0001c0001t0042g0257a0001c0001t0114g0254others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1140+1593A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92144887 | ||||||
chr14:92145136
|
A | T | 32 | a0001c0001t0020g0011a0001c0001t0021g0004a0001c0001t0021g0126others(29): Show | 37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1140+1842A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145136 | ||||||
chr14:92145144
|
T | G | 6 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(3): Show | 6 | HG01255.hp2 HG03041.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1140+1850T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145144 | ||||||
chr14:92145290
|
G | A | 1 | a0001c0001t0113g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1140+1996G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145290 | ||||||
chr14:92145346
|
A | C | 62 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(59): Show | 77 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1140+2052A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145346 | ||||||
chr14:92145346
|
A | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.1140+2052A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145346 | ||||||
chr14:92145355
|
T | TA | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1140+2063dupA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92145355 | |||||
chr14:92145626
|
A | G | 1 | a0001c0001t0016g0198 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1140+2332A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145626 | ||||||
chr14:92145655
|
C | G | 134 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 163 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.1140+2361C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145655 | ||||||
chr14:92145738
|
A | C | 1 | a0001c0001t0166g0103 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1140+2444A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145738 | ||||||
chr14:92145870
|
C | G | 1 | a0001c0001t0094g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1140+2576C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145870 | ||||||
chr14:92145969
|
T | A | 1 | a0001c0001t0002g0020 | 3 | HG01168.hp1 HG01169.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1140+2675T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145969 | ||||||
chr14:92146093
|
A | G | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1140+2799A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146093 | ||||||
chr14:92146099
|
A | AT | 5 | a0001c0001t0003g0029a0001c0001t0003g0101a0001c0001t0010g0100others(2): Show | 5 | NA18952.hp2 NA18960.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.1140+2805_1140+280 others(5): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146099 | ||||||
chr14:92146194
|
G | T | 1 | a0001c0001t0047g0092 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1140+2900G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146194 | ||||||
chr14:92146296
|
C | T | 1 | a0001c0001t0139g0082 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1140+3002C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146296 | ||||||
chr14:92146303
|
C | T | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1140+3009C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146303 | ||||||
chr14:92146387
|
G | C | 1 | a0001c0001t0151g0064 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1140+3093G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146387 | ||||||
chr14:92146503
|
A | G | 1 | a0001c0001t0005g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1140+3209A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146503 | ||||||
chr14:92146523
|
AAAAC | A | 12 | a0001c0001t0042g0252a0001c0001t0042g0257a0001c0001t0114g0254others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1140+3237_1140+324 others(8): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92146523 | |||||
chr14:92146554
|
C | G | 1 | a0001c0001t0040g0034 | 2 | HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1140+3260C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146554 | ||||||
chr14:92146720
|
C | CTT | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1140+3427_1140+342 others(6): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92146720 | |||||
chr14:92146854
|
C | T | 69 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 81 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1140+3560C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146854 | ||||||
chr14:92146957
|
C | G | 5 | a0001c0001t0001g0012a0001c0001t0001g0146a0001c0001t0001g0162others(2): Show | 7 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(4): Show |
intron_variant | MODIFIER | c.1140+3663C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146957 | ||||||
chr14:92146990
|
AC | A | 32 | a0001c0001t0020g0011a0001c0001t0021g0004a0001c0001t0021g0126others(29): Show | 37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1140+3698delC | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92146990 | |||||
chr14:92147219
|
G | C | 1 | a0001c0001t0034g0105 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1140+3925G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92147219 | ||||||
chr14:92147254
|
A | G | 2 | a0001c0001t0002g0008a0001c0001t0101g0008 | 5 | HG03490.hp2 HG03492.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1140+3960A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92147254 | ||||||
chr14:92147409
|
T | C | 32 | a0001c0001t0020g0011a0001c0001t0021g0004a0001c0001t0021g0126others(29): Show | 37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1140+4115T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92147409 | ||||||
chr14:92147630
|
A | C | 94 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(91): Show | 95 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1140+4336A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92147630 | ||||||
chr14:92147860
|
A | G | 1 | a0001c0001t0113g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1140+4566A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92147860 | ||||||
chr14:92147894
|
A | T | 1 | a0001c0001t0002g0222 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1140+4600A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92147894 | ||||||
chr14:92147902
|
A | T | 278 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(275): Show | 313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.1140+4608A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92147902 | ||||||
chr14:92147958
|
C | T | 3 | a0001c0001t0099g0227a0001c0001t0100g0243a0001c0001t0109g0242 | 3 | HG01175.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1140+4664C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92147958 | ||||||
chr14:92147980
|
C | T | 1 | a0001c0001t0168g0087 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1140+4686C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92147980 | ||||||
chr14:92148131
|
C | G | 93 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(90): Show | 94 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1140+4837C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148131 | ||||||
chr14:92148178
|
T | C | 1 | a0001c0001t0146g0056 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1140+4884T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148178 | ||||||
chr14:92148310
|
T | G | 5 | a0001c0001t0026g0150a0001c0001t0026g0151a0001c0001t0026g0153others(2): Show | 5 | HG02486.hp2 HG03041.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1140+5016T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148310 | ||||||
chr14:92148360
|
G | C | 2 | a0001c0001t0068g0125a0001c0001t0069g0124 | 2 | NA18946.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1140+5066G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148360 | ||||||
chr14:92148397
|
G | A | 144 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(141): Show | 150 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1140+5103G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148397 | ||||||
chr14:92148483
|
C | T | 3 | a0001c0001t0042g0252a0001c0001t0042g0257a0001c0001t0121g0258 | 3 | HG02145.hp2 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1140+5189C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148483 | ||||||
chr14:92148494
|
A | G | 1 | a0001c0001t0006g0210 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1140+5200A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148494 | ||||||
chr14:92148540
|
A | G | 12 | a0001c0001t0042g0252a0001c0001t0042g0257a0001c0001t0114g0254others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1140+5246A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148540 | ||||||
chr14:92148664
|
G | T | 2 | a0001c0001t0003g0026a0001c0001t0047g0026 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1140+5370G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148664 | ||||||
chr14:92148771
|
C | CA | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1140+5493dupA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92148771 | |||||
chr14:92148771
|
CA | C | 6 | a0001c0001t0001g0161a0001c0001t0009g0145a0001c0001t0025g0176others(3): Show | 6 | HG02451.hp1 HG02965.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.1140+5493delA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92148771 | |||||
chr14:92148797
|
G | GTA | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1140+5515_1140+551 others(6): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92148797 | |||||
chr14:92148808
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1140+5514T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148808 | ||||||
chr14:92149031
|
C | A | 145 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(142): Show | 151 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.1141-5327C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149031 | ||||||
chr14:92149119
|
T | TACTGGTA others(8): Show |
1 | a0001c0001t0060g0116 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1141-5238_1141-522 others(19): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92149119 | |||||
chr14:92149147
|
C | T | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1141-5211C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149147 | ||||||
chr14:92149155
|
A | G | 1 | a0001c0001t0088g0160 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1141-5203A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149155 | ||||||
chr14:92149213
|
A | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0168a0001c0001t0008g0005others(4): Show | 10 | NA18961.hp1 NA18965.hp1 NA18999.hp1 others(7): Show |
intron_variant | MODIFIER | c.1141-5145A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149213 | ||||||
chr14:92149369
|
G | A | 1 | a0001c0001t0129g0215 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1141-4989G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149369 | ||||||
chr14:92149397
|
C | CAT | 140 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(137): Show | 146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1141-4960_1141-495 others(6): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92149397 | |||||
chr14:92149481
|
C | T | 1 | a0001c0001t0006g0217 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1141-4877C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149481 | ||||||
chr14:92149573
|
G | T | 1 | a0001c0001t0004g0081 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1141-4785G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149573 | ||||||
chr14:92149665
|
G | GT | 37 | a0001c0001t0016g0131a0001c0001t0020g0011a0001c0001t0021g0004others(34): Show | 42 | HG00408.hp2 HG02040.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.1141-4684dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92149665 | |||||
chr14:92149725
|
G | A | 1 | a0001c0001t0005g0199 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1141-4633G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149725 | ||||||
chr14:92149741
|
C | T | 2 | a0001c0001t0003g0099a0001c0001t0113g0253 | 2 | HG02809.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1141-4617C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149741 | ||||||
chr14:92149742
|
G | A | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1141-4616G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149742 | ||||||
chr14:92149817
|
G | A | 140 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(137): Show | 146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1141-4541G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149817 | ||||||
chr14:92149821
|
G | A | 202 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(199): Show | 223 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.1141-4537G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149821 | ||||||
chr14:92149858
|
T | C | 32 | a0001c0001t0020g0011a0001c0001t0021g0004a0001c0001t0021g0126others(29): Show | 37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1141-4500T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149858 | ||||||
chr14:92149947
|
G | A | 1 | a0001c0001t0053g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1141-4411G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149947 | ||||||
chr14:92150112
|
T | C | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1141-4246T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150112 | ||||||
chr14:92150126
|
A | ATT | 278 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(275): Show | 313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.1141-4223_1141-422 others(6): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92150126 | |||||
chr14:92150179
|
C | T | 145 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(142): Show | 151 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.1141-4179C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150179 | ||||||
chr14:92150193
|
C | T | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1141-4165C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150193 | ||||||
chr14:92150414
|
A | T | 1 | a0001c0001t0025g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1141-3944A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150414 | ||||||
chr14:92150415
|
C | A | 1 | a0001c0001t0025g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1141-3943C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150415 | ||||||
chr14:92150427
|
T | TTG | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1141-3921_1141-392 others(6): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92150427 | |||||
chr14:92150437
|
G | T | 1 | a0001c0001t0128g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1141-3921G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150437 | ||||||
chr14:92150438
|
T | TG | 4 | a0001c0001t0026g0150a0001c0001t0026g0151a0001c0001t0026g0153others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1141-3920_1141-391 others(5): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150438 | ||||||
chr14:92150439
|
T | G | 1 | a0001c0001t0100g0243 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1141-3919T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150439 | ||||||
chr14:92150622
|
C | G | 1 | a0001c0001t0013g0212 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1141-3736C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150622 | ||||||
chr14:92150700
|
A | G | 1 | a0001c0001t0010g0063 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1141-3658A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150700 | ||||||
chr14:92151002
|
A | G | 1 | a0001c0001t0010g0080 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1141-3356A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151002 | ||||||
chr14:92151436
|
TA | T | 51 | a0001c0001t0001g0005a0001c0001t0001g0168a0001c0001t0008g0005others(48): Show | 60 | HG00408.hp2 HG01069.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.1141-2907delA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92151436 | |||||
chr14:92151437
|
A | T | 58 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(55): Show | 73 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1141-2921A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151437 | ||||||
chr14:92151438
|
A | T | 2 | a0001c0001t0013g0188a0001c0001t0124g0245 | 2 | HG02055.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1141-2920A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151438 | ||||||
chr14:92151451
|
A | T | 92 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(89): Show | 93 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1141-2907A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151451 | ||||||
chr14:92151452
|
TTAACAC | T | 92 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(89): Show | 93 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1141-2905_1141-290 others(10): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151452 | ||||||
chr14:92151453
|
T | C | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1141-2905T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151453 | ||||||
chr14:92151455
|
A | C | 7 | a0001c0001t0002g0020a0001c0001t0002g0043a0001c0001t0002g0220others(4): Show | 9 | HG00099.hp2 HG00642.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1141-2903A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151455 | ||||||
chr14:92151669
|
G | C | 1 | a0001c0001t0160g0067 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1141-2689G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151669 | ||||||
chr14:92151866
|
G | A | 3 | a0001c0001t0014g0248a0001c0001t0014g0249a0001c0001t0014g0250 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1141-2492G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151866 | ||||||
chr14:92151925
|
T | G | 139 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(136): Show | 145 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1141-2433T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151925 | ||||||
chr14:92152010
|
CA | C | 62 | a0001c0001t0001g0183a0001c0001t0002g0001a0001c0001t0002g0008others(59): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.1141-2331delA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92152010 | |||||
chr14:92152010
|
CAA | C | 176 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 209 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.1141-2332_1141-233 others(6): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92152010 | |||||
chr14:92152010
|
CAAA | C | 91 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(88): Show | 92 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1141-2333_1141-233 others(7): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92152010 | |||||
chr14:92152035
|
C | T | 1 | a0001c0001t0011g0046 | 2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1141-2323C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152035 | ||||||
chr14:92152159
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1141-2199C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152159 | ||||||
chr14:92152215
|
C | T | 1 | a0001c0001t0134g0207 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1141-2143C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152215 | ||||||
chr14:92152237
|
C | T | 1 | a0001c0001t0052g0039 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1141-2121C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152237 | ||||||
chr14:92152271
|
A | C | 1 | a0001c0001t0008g0159 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1141-2087A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152271 | ||||||
chr14:92152337
|
C | T | 1 | a0001c0001t0010g0080 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1141-2021C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152337 | ||||||
chr14:92152381
|
G | A | 1 | a0001c0001t0008g0173 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1141-1977G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152381 | ||||||
chr14:92152424
|
C | T | 1 | a0001c0001t0134g0207 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1141-1934C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152424 | ||||||
chr14:92152455
|
T | C | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1141-1903T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152455 | ||||||
chr14:92152651
|
C | T | 94 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(91): Show | 95 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1141-1707C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152651 | ||||||
chr14:92152659
|
G | T | 1 | a0001c0001t0004g0081 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1141-1699G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152659 | ||||||
chr14:92152821
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1141-1537T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152821 | ||||||
chr14:92152991
|
C | CT | 58 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(55): Show | 73 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.1141-1358dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92152991 | |||||
chr14:92152991
|
CTT | C | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1141-1359_1141-135 others(6): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92152991 | |||||
chr14:92153051
|
G | T | 32 | a0001c0001t0020g0011a0001c0001t0021g0004a0001c0001t0021g0126others(29): Show | 37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1141-1307G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92153051 | ||||||
chr14:92153058
|
A | G | 1 | a0001c0001t0046g0068 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1141-1300A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92153058 | ||||||
chr14:92153061
|
T | TCAAATTT others(2603): Show |
2 | a0001c0001t0114g0254a0001c0001t0115g0255 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2614): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2603): Show |
1 | a0001c0001t0122g0256 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2614): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2608): Show |
2 | a0001c0001t0033g0032a0001c0001t0070g0032 | 2 | HG02523.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2619): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2608): Show |
20 | a0001c0001t0020g0011a0001c0001t0021g0004a0001c0001t0031g0004others(17): Show | 24 | HG02040.hp2 HG02165.hp1 HG03491.hp1 others(21): Show |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2619): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2609): Show |
1 | a0001c0001t0060g0116 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2620): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2609): Show |
2 | a0001c0001t0034g0031a0001c0001t0036g0031 | 2 | NA18950.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2620): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2611): Show |
1 | a0001c0001t0064g0122 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2622): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2610): Show |
1 | a0001c0001t0021g0126 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2621): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2609): Show |
1 | a0001c0001t0021g0127 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2620): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2609): Show |
2 | a0001c0001t0032g0033a0001c0001t0066g0115 | 3 | NA18989.hp1 NA18997.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2620): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2621): Show |
1 | a0001c0001t0056g0128 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2632): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2627): Show |
1 | a0001c0001t0062g0123 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2638): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2482): Show |
1 | a0001c0001t0003g0070 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2493): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2613): Show |
1 | a0001c0001t0166g0103 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2624): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2614): Show |
1 | a0001c0001t0004g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2613): Show |
2 | a0001c0001t0003g0026a0001c0001t0047g0026 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2624): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2483): Show |
2 | a0001c0001t0140g0024a0001c0001t0153g0024 | 2 | HG02165.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2494): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2483): Show |
1 | a0001c0001t0004g0061 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2494): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2484): Show |
1 | a0001c0001t0019g0086 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2495): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2614): Show |
1 | a0001c0001t0004g0060 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2614): Show |
27 | a0001c0001t0003g0009a0001c0001t0003g0028a0001c0001t0003g0029others(24): Show | 28 | HG00423.hp2 HG01258.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2614): Show |
2 | a0001c0001t0003g0099a0001c0001t0019g0098 | 2 | NA19085.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2613): Show |
1 | a0001c0001t0003g0058 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2624): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2615): Show |
1 | a0001c0001t0046g0068 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2626): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2616): Show |
1 | a0001c0001t0003g0057 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2627): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2614): Show |
1 | a0001c0001t0019g0112 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2614): Show |
1 | a0001c0001t0146g0056 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2614): Show |
1 | a0001c0001t0029g0140 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2615): Show |
1 | a0001c0001t0004g0108 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2626): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2615): Show |
1 | a0001c0001t0004g0072 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2626): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2615): Show |
3 | a0001c0001t0003g0055a0001c0001t0018g0073a0001c0001t0154g0093 | 3 | NA18961.hp2 NA18988.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2626): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2616): Show |
1 | a0001c0001t0019g0094 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2627): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2617): Show |
1 | a0001c0001t0004g0095 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2628): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2617): Show |
1 | a0001c0001t0003g0101 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2628): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2616): Show |
1 | a0001c0001t0158g0069 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2627): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2484): Show |
5 | a0001c0001t0003g0010a0001c0001t0004g0010a0001c0001t0010g0010others(2): Show | 5 | HG01074.hp2 HG01934.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2495): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2615): Show |
1 | a0001c0001t0148g0134 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2626): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2615): Show |
2 | a0001c0001t0003g0089a0001c0001t0150g0091 | 2 | NA18941.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2626): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2615): Show |
12 | a0001c0001t0003g0025a0001c0001t0003g0107a0001c0001t0004g0025others(9): Show | 12 | HG00438.hp2 HG00558.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2626): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2616): Show |
1 | a0001c0001t0155g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2627): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2617): Show |
1 | a0001c0001t0018g0076 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2628): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2618): Show |
1 | a0001c0001t0048g0113 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2629): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2618): Show |
1 | a0001c0001t0139g0082 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2629): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2617): Show |
1 | a0001c0001t0003g0109 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2628): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2615): Show |
1 | a0001c0001t0010g0114 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2626): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2616): Show |
4 | a0001c0001t0003g0066a0001c0001t0004g0027a0001c0001t0048g0137others(1): Show | 4 | HG03209.hp2 NA18949.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2627): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2619): Show |
1 | a0001c0001t0168g0087 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2630): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2621): Show |
1 | a0001c0001t0004g0085 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2632): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2617): Show |
1 | a0001c0001t0004g0077 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2628): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2618): Show |
1 | a0001c0001t0029g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2629): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2614): Show |
1 | a0001c0001t0050g0102 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2200): Show |
1 | a0001c0001t0113g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2211): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2614): Show |
1 | a0002c0002t0010g0078 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2616): Show |
1 | a0001c0001t0003g0059 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2627): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2611): Show |
1 | a0001c0001t0118g0261 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2622): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2611): Show |
1 | a0001c0001t0165g0259 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2622): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2612): Show |
5 | a0001c0001t0042g0252a0001c0001t0116g0023a0001c0001t0117g0023others(2): Show | 5 | HG02922.hp1 HG02970.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2623): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2614): Show |
1 | a0001c0001t0121g0258 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2613): Show |
1 | a0001c0001t0042g0257 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2624): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2613): Show |
1 | a0001c0001t0010g0063 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2624): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2614): Show |
2 | a0001c0001t0049g0079a0001c0001t0049g0090 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153061
|
T | TCAAATTT others(2615): Show |
1 | a0001c0001t0010g0097 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2626): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | |||||
chr14:92153482
|
T | C | 2 | a0001c0001t0129g0215a0001c0001t0132g0202 | 2 | HG01167.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1141-876T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92153482 | ||||||
chr14:92153529
|
A | G | 1 | a0001c0001t0145g0083 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1141-829A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92153529 | ||||||
chr14:92153703
|
C | CT | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 161 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.1141-639dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153703 | |||||
chr14:92153734
|
T | C | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
intron_variant | MODIFIER | c.1141-624T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92153734 | ||||||
chr14:92153866
|
C | CT | 22 | a0001c0001t0001g0167a0001c0001t0001g0181a0001c0001t0003g0057others(19): Show | 22 | HG01884.hp1 HG01934.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.1141-472dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153866 | |||||
chr14:92153866
|
C | CTTT | 29 | a0001c0001t0004g0081a0001c0001t0020g0011a0001c0001t0021g0004others(26): Show | 34 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(31): Show |
intron_variant | MODIFIER | c.1141-474_1141-472d others(5): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153866 | |||||
chr14:92153867
|
T | G | 1 | a0001c0001t0102g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1141-491T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92153867 | ||||||
chr14:92153886
|
T | A | 1 | a0001c0001t0026g0150 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1141-472T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92153886 | ||||||
chr14:92153886
|
T | TA | 4 | a0001c0001t0026g0151a0001c0001t0026g0153a0001c0001t0085g0154others(1): Show | 4 | HG02486.hp2 HG03041.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1141-471dupA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153886 | |||||
chr14:92153907
|
T | G | 1 | a0001c0001t0113g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1141-451T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92153907 | ||||||
chr14:92154092
|
A | G | 6 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(3): Show | 6 | HG01255.hp2 HG03041.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1141-266A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92154092 | ||||||
chr14:92154159
|
A | T | 1 | a0001c0001t0113g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1141-199A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92154159 | ||||||
chr14:92154480
|
T | G | 2 | a0001c0001t0003g0133a0001c0001t0004g0138 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1241+22T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 10/15 | chr14 | 92154480 | ||||||
chr14:92154566
|
AT | A | 4 | a0001c0001t0003g0057a0001c0001t0003g0058a0001c0001t0004g0053others(1): Show | 4 | NA18954.hp1 NA18966.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241+112delT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr14 | 92154566 | |||||
chr14:92154710
|
G | T | 8 | a0001c0001t0003g0133a0001c0001t0004g0138a0001c0001t0029g0135others(5): Show | 8 | HG01891.hp1 HG02622.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1241+252G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 10/15 | chr14 | 92154710 | ||||||
chr14:92154747
|
A | G | 1 | a0001c0001t0004g0085 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1241+289A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 10/15 | chr14 | 92154747 | ||||||
chr14:92154842
|
A | G | 1 | a0001c0001t0109g0242 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1242-281A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 10/15 | chr14 | 92154842 | ||||||
chr14:92154951
|
T | C | 3 | a0001c0001t0014g0248a0001c0001t0014g0249a0001c0001t0014g0250 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1242-172T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 10/15 | chr14 | 92154951 | ||||||
chr14:92154956
|
G | A | 2 | a0001c0001t0068g0125a0001c0001t0069g0124 | 2 | NA18946.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1242-167G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 10/15 | chr14 | 92154956 | ||||||
chr14:92155033
|
T | C | 1 | a0001c0001t0095g0224 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1242-90T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 10/15 | chr14 | 92155033 | ||||||
chr14:92155490
|
A | G | 1 | a0001c0001t0142g0054 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1442+167A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92155490 | ||||||
chr14:92155560
|
G | A | 95 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(92): Show | 96 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1442+237G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92155560 | ||||||
chr14:92155584
|
G | A | 3 | a0001c0001t0003g0133a0001c0001t0004g0138a0001c0001t0048g0137 | 3 | HG02970.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1442+261G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92155584 | ||||||
chr14:92155600
|
T | A | 1 | a0001c0001t0151g0064 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1442+277T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92155600 | ||||||
chr14:92155770
|
TA | T | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
intron_variant | MODIFIER | c.1442+460delA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr14 | 92155770 | |||||
chr14:92155806
|
G | A | 1 | a0001c0001t0010g0114 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1442+483G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92155806 | ||||||
chr14:92155811
|
T | A | 145 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(142): Show | 151 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.1442+488T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92155811 | ||||||
chr14:92155959
|
A | G | 3 | a0001c0001t0005g0018a0001c0001t0006g0018a0001c0001t0013g0186 | 4 | NA18980.hp2 NA18986.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1443-520A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92155959 | ||||||
chr14:92155967
|
A | G | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1443-512A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92155967 | ||||||
chr14:92155980
|
G | A | 145 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(142): Show | 151 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.1443-499G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92155980 | ||||||
chr14:92156021
|
G | A | 1 | a0001c0001t0007g0044 | 2 | HG01433.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1443-458G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92156021 | ||||||
chr14:92156060
|
C | T | 1 | a0001c0001t0124g0245 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1443-419C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92156060 | ||||||
chr14:92156107
|
G | A | 2 | a0001c0001t0002g0230a0001c0001t0110g0228 | 2 | HG01081.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1443-372G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92156107 | ||||||
chr14:92156167
|
G | A | 1 | a0001c0001t0024g0157 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1443-312G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92156167 | ||||||
chr14:92156297
|
C | A | 1 | a0001c0001t0013g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1443-182C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92156297 | ||||||
chr14:92156335
|
T | A | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.1443-144T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92156335 | ||||||
chr14:92156343
|
C | T | 1 | a0001c0001t0005g0206 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1443-136C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92156343 | ||||||
chr14:92156711
|
C | T | 1 | a0001c0001t0129g0215 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1595+80C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | chr14 | 92156711 | ||||||
chr14:92156754
|
A | AAATTT | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
intron_variant | MODIFIER | c.1595+125_1595+129d others(7): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 92156754 | |||||
chr14:92156953
|
C | T | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1595+322C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | chr14 | 92156953 | ||||||
chr14:92157005
|
A | G | 140 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(137): Show | 146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1595+374A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | chr14 | 92157005 | ||||||
chr14:92157069
|
C | A | 1 | a0001c0001t0009g0163 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1595+438C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | chr14 | 92157069 | ||||||
chr14:92157520
|
C | T | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
intron_variant | MODIFIER | c.1596-139C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | chr14 | 92157520 | ||||||
chr14:92157521
|
AAAAAT | A | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596-129_1596-125d others(7): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 92157521 | |||||
chr14:92157552
|
CAT | C | 96 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(93): Show | 98 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1596-106_1596-105d others(4): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | chr14 | 92157552 | ||||||
chr14:92157604
|
A | T | 1 | a0001c0001t0026g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1596-55A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | chr14 | 92157604 | ||||||
chr14:92157645
|
A | G | 4 | a0001c0001t0005g0218a0001c0001t0017g0201a0001c0001t0043g0042others(1): Show | 5 | HG02280.hp1 HG02451.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596-14A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | chr14 | 92157645 | ||||||
chr14:92157946
|
GATAAC | G | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1821+65_1821+69del others(5): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | 92157946 | |||||
chr14:92158018
|
A | T | 2 | a0001c0001t0003g0026a0001c0001t0047g0026 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1821+134A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/15 | chr14 | 92158018 | ||||||
chr14:92158174
|
T | G | 12 | a0001c0001t0042g0252a0001c0001t0042g0257a0001c0001t0114g0254others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1821+290T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/15 | chr14 | 92158174 | ||||||
chr14:92158303
|
C | T | 10 | a0001c0001t0005g0018a0001c0001t0006g0014a0001c0001t0006g0018others(7): Show | 12 | HG00621.hp1 HG02015.hp2 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.1821+419C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/15 | chr14 | 92158303 | ||||||
chr14:92158305
|
G | A | 1 | a0001c0001t0003g0071 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1821+421G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/15 | chr14 | 92158305 | ||||||
chr14:92158722
|
C | T | 1 | a0001c0001t0113g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1822-261C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/15 | chr14 | 92158722 | ||||||
chr14:92158723
|
G | A | 95 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(92): Show | 96 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1822-260G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/15 | chr14 | 92158723 | ||||||
chr14:92158843
|
G | A | 1 | a0001c0001t0079g0158 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1822-140G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/15 | chr14 | 92158843 | ||||||
chr14:92158964
|
C | T | 12 | a0001c0001t0042g0252a0001c0001t0042g0257a0001c0001t0114g0254others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1822-19C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/15 | chr14 | 92158964 | ||||||
chr14:92159427
|
C | G | 1 | a0001c0001t0127g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2121+145C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92159427 | ||||||
chr14:92159545
|
G | A | 1 | a0001c0001t0044g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2121+263G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92159545 | ||||||
chr14:92159559
|
A | G | 145 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(142): Show | 151 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.2121+277A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92159559 | ||||||
chr14:92159576
|
G | C | 2 | a0001c0001t0002g0045a0001c0001t0167g0045 | 2 | HG00323.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.2121+294G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92159576 | ||||||
chr14:92159792
|
A | G | 1 | a0001c0001t0168g0087 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2121+510A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92159792 | ||||||
chr14:92159929
|
A | G | 2 | a0001c0001t0029g0136a0001c0001t0148g0134 | 2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2121+647A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92159929 | ||||||
chr14:92159933
|
T | G | 2 | a0001c0001t0053g0213a0001c0001t0054g0214 | 2 | HG00558.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2121+651T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92159933 | ||||||
chr14:92159942
|
A | G | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2121+660A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92159942 | ||||||
chr14:92159953
|
G | GT | 153 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(150): Show | 169 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.2121+681dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr14 | 92159953 | |||||
chr14:92159994
|
G | A | 95 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(92): Show | 96 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.2121+712G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92159994 | ||||||
chr14:92160072
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.2121+790C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160072 | ||||||
chr14:92160144
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2121+862G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160144 | ||||||
chr14:92160151
|
C | T | 1 | a0001c0001t0064g0122 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2121+869C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160151 | ||||||
chr14:92160194
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.2121+912C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160194 | ||||||
chr14:92160250
|
A | C | 140 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(137): Show | 146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.2122-862A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160250 | ||||||
chr14:92160251
|
A | G | 4 | a0001c0001t0014g0248a0001c0001t0014g0249a0001c0001t0014g0250others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2122-861A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160251 | ||||||
chr14:92160436
|
A | G | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0014g0249others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2122-676A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160436 | ||||||
chr14:92160501
|
G | A | 1 | a0001c0001t0159g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2122-611G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160501 | ||||||
chr14:92160663
|
A | G | 4 | a0001c0001t0006g0210a0001c0001t0013g0216a0001c0001t0137g0204others(1): Show | 4 | HG00673.hp1 HG02080.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.2122-449A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160663 | ||||||
chr14:92160706
|
A | G | 1 | a0001c0001t0157g0106 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2122-406A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160706 | ||||||
chr14:92160725
|
C | T | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
intron_variant | MODIFIER | c.2122-387C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160725 | ||||||
chr14:92160746
|
G | A | 1 | a0001c0001t0166g0103 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2122-366G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160746 | ||||||
chr14:92160794
|
G | T | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
intron_variant | MODIFIER | c.2122-318G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160794 | ||||||
chr14:92160816
|
G | A | 57 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0040others(54): Show | 72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.2122-296G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160816 | ||||||
chr14:92160996
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 91 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.2122-116C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160996 | ||||||
chr14:92161065
|
C | T | 3 | a0001c0001t0010g0063a0001c0001t0049g0079a0001c0001t0049g0090 | 3 | HG01069.hp1 HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.2122-47C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92161065 | ||||||
chr14:92161308
|
A | C | 4 | a0001c0001t0005g0218a0001c0001t0017g0201a0001c0001t0043g0042others(1): Show | 5 | HG02280.hp1 HG02451.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2256+62A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 15/15 | chr14 | 92161308 | ||||||
chr14:92161324
|
T | A | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
intron_variant | MODIFIER | c.2256+78T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 15/15 | chr14 | 92161324 | ||||||
chr14:92161357
|
T | G | 32 | a0001c0001t0020g0011a0001c0001t0021g0004a0001c0001t0021g0126others(29): Show | 37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.2256+111T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 15/15 | chr14 | 92161357 | ||||||
chr14:92161366
|
T | C | 140 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0025others(137): Show | 146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.2256+120T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 15/15 | chr14 | 92161366 | ||||||
chr14:92161562
|
A | G | 1 | a0001c0001t0113g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2257-90A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 15/15 | chr14 | 92161562 |