Item | Value |
---|---|
geneid | 167227 |
ensemblid | ENSG00000172795.17 |
hgncid | 24452 |
symbol | DCP2 |
name | decapping mRNA 2 |
refseq_nuc | NM_152624.6 |
refseq_prot | NP_689837.2 |
ensembl_nuc | ENST00000389063.3 |
ensembl_prot | ENSP00000373715.2 |
mane_status | MANE Select |
chr | chr5 |
start | 112976798 |
end | 113022195 |
strand | + |
ver | v1.2 |
region | chr5:112976798-113022195 |
region5000 | chr5:112971798-113027195 |
regionname0 | DCP2_chr5_112976798_113022195 |
regionname5000 | DCP2_chr5_112971798_113027195 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 420 | 364 | 96 | 60 | 158 | 14 | 34 | 128 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1263 | 252 | 67 | 38 | 107 | 11 | 28 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
c0002 | 1/0 | 1263 | 86 | 13 | 20 | 44 | 3 | 5 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
c0003 | 0/0 | 1263 | 9 | 9 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
c0004 | 0/0 | 1263 | 6 | 4 | 1 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
c0005 | 0/0 | 1263 | 3 | 0 | 0 | 3 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
c0006 | 0/0 | 1263 | 3 | 0 | 0 | 3 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
c0007 | 0/0 | 1263 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
c0008 | 0/0 | 1263 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
c0009 | 0/0 | 1263 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
c0010 | 0/0 | 1263 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
c0011 | 0/0 | 1263 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 8846 | 77 | 3 | 19 | 40 | 3 | 11 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0002 | 0/0 | 8848 | 39 | 6 | 15 | 13 | 2 | 3 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0003 | 0/0 | 8847 | 24 | 5 | 1 | 11 | 2 | 5 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0004 | 0/0 | 8847 | 13 | 0 | 3 | 10 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0005 | 0/0 | 8846 | 12 | 12 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0006 | 0/0 | 8847 | 11 | 1 | 0 | 9 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0007 | 0/0 | 8846 | 10 | 1 | 0 | 9 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0008 | 0/0 | 8850 | 9 | 0 | 2 | 7 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0009 | 0/0 | 8849 | 5 | 0 | 0 | 5 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0010 | 0/0 | 8846 | 5 | 0 | 0 | 5 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0011 | 0/0 | 8848 | 5 | 5 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0012 | 0/0 | 8851 | 5 | 4 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0013 | 0/0 | 8847 | 5 | 4 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0014 | 0/0 | 8848 | 4 | 0 | 0 | 4 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0015 | 0/0 | 8847 | 4 | 4 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0016 | 0/0 | 8847 | 4 | 0 | 0 | 2 | 2 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0017 | 0/0 | 8847 | 4 | 4 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0018 | 0/0 | 8851 | 4 | 4 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0019 | 0/0 | 8842 | 3 | 2 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0020 | 0/0 | 8850 | 3 | 0 | 0 | 3 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0021 | 0/0 | 8846 | 3 | 0 | 2 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0022 | 0/0 | 8845 | 3 | 3 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0023 | 0/0 | 8846 | 3 | 3 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0024 | 0/0 | 8848 | 3 | 3 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0025 | 0/0 | 8848 | 2 | 1 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0026 | 0/0 | 8848 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0027 | 0/0 | 8849 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0028 | 0/0 | 8849 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0029 | 0/0 | 8846 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0030 | 0/0 | 8847 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0031 | 0/0 | 8848 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0032 | 0/0 | 8847 | 2 | 0 | 0 | 0 | 0 | 2 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0033 | 0/0 | 8847 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0034 | 0/0 | 8848 | 2 | 0 | 0 | 0 | 0 | 2 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0035 | 0/0 | 8846 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0036 | 0/0 | 8846 | 2 | 0 | 2 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0037 | 0/0 | 8846 | 2 | 0 | 0 | 0 | 2 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0038 | 0/0 | 8847 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0039 | 1/0 | 8848 | 2 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0040 | 0/0 | 8846 | 2 | 0 | 2 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0041 | 0/0 | 8848 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0042 | 0/0 | 8846 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0043 | 0/0 | 8848 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0044 | 0/0 | 8849 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0045 | 0/0 | 8846 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0046 | 0/0 | 8848 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0047 | 0/0 | 8849 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0048 | 0/0 | 8848 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0049 | 0/0 | 8848 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0050 | 0/0 | 8848 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0051 | 0/0 | 8849 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0052 | 0/0 | 8847 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0053 | 0/0 | 8849 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0054 | 0/0 | 8847 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0055 | 0/0 | 8847 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0056 | 0/0 | 8849 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0057 | 0/0 | 8849 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0058 | 0/0 | 8850 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0059 | 0/0 | 8850 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0060 | 0/0 | 8843 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0061 | 0/0 | 8851 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0062 | 0/0 | 8843 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0063 | 0/0 | 8848 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0064 | 0/0 | 8848 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0065 | 0/0 | 8846 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0066 | 0/0 | 8845 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0067 | 0/0 | 8848 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0068 | 0/0 | 8847 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0069 | 0/0 | 8849 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0070 | 0/0 | 8848 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0071 | 0/0 | 8847 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0072 | 0/0 | 8847 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0073 | 0/0 | 8847 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0074 | 0/0 | 8847 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0075 | 0/0 | 8847 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0076 | 0/0 | 8849 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0077 | 0/0 | 8849 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0078 | 0/0 | 8848 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0079 | 0/0 | 8847 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0080 | 0/0 | 8846 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0081 | 0/0 | 8845 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0082 | 0/0 | 8846 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0083 | 0/0 | 8846 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0084 | 0/0 | 8846 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0085 | 0/0 | 8846 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0086 | 0/0 | 8846 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0087 | 0/0 | 8847 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0088 | 0/0 | 8846 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0089 | 0/0 | 8846 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0090 | 0/0 | 8846 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0091 | 0/0 | 8846 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0092 | 0/0 | 8846 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0093 | 0/0 | 8847 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0094 | 0/0 | 8846 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0095 | 0/0 | 8847 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0096 | 0/0 | 8846 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0097 | 0/0 | 8847 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0098 | 0/0 | 8846 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0099 | 0/0 | 8847 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0100 | 0/0 | 8846 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0101 | 0/0 | 8846 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0102 | 0/0 | 8848 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0103 | 0/0 | 8848 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0104 | 0/0 | 8848 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0105 | 0/0 | 8847 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0106 | 0/0 | 8848 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0107 | 0/0 | 8849 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0108 | 0/0 | 8851 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0109 | 0/0 | 8850 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0110 | 0/0 | 8847 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0111 | 0/0 | 8847 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0112 | 0/0 | 8848 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0113 | 0/0 | 8848 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
t0114 | 0/0 | 8848 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0004 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0231 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0283 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1263 | 252 | 67 | 38 | 107 | 11 | 28 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
a0001c0002 | 1/0 | 1263 | 86 | 13 | 20 | 44 | 3 | 5 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
a0001c0003 | 0/0 | 1263 | 9 | 9 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
a0001c0004 | 0/0 | 1263 | 6 | 4 | 1 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
a0001c0005 | 0/0 | 1263 | 3 | 0 | 0 | 3 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
a0001c0006 | 0/0 | 1263 | 3 | 0 | 0 | 3 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
a0001c0007 | 0/0 | 1263 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
a0001c0008 | 0/0 | 1263 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
a0001c0009 | 0/0 | 1263 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
a0001c0010 | 0/0 | 1263 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 | |
a0001c0011 | 0/0 | 1263 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 10108 | 76 | 3 | 18 | 40 | 3 | 11 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0003 | 0/0 | 10109 | 24 | 5 | 1 | 11 | 2 | 5 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0004 | 0/0 | 10109 | 10 | 0 | 3 | 7 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0005 | 0/0 | 10108 | 3 | 3 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0006 | 0/0 | 10109 | 11 | 1 | 0 | 9 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0007 | 0/0 | 10108 | 10 | 1 | 0 | 9 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0010 | 0/0 | 10108 | 5 | 0 | 0 | 5 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0011 | 0/0 | 10110 | 5 | 5 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0012 | 0/0 | 10113 | 5 | 4 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0013 | 0/0 | 10109 | 5 | 4 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0015 | 0/0 | 10109 | 4 | 4 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0016 | 0/0 | 10109 | 4 | 0 | 0 | 2 | 2 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0017 | 0/0 | 10109 | 4 | 4 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0018 | 0/0 | 10113 | 4 | 4 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0020 | 0/0 | 10112 | 3 | 0 | 0 | 3 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0021 | 0/0 | 10108 | 2 | 0 | 2 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0022 | 0/0 | 10107 | 3 | 3 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0023 | 0/0 | 10108 | 3 | 3 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0024 | 0/0 | 10110 | 3 | 3 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0029 | 0/0 | 10108 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0030 | 0/0 | 10109 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0031 | 0/0 | 10110 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0032 | 0/0 | 10109 | 2 | 0 | 0 | 0 | 0 | 2 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0033 | 0/0 | 10109 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0034 | 0/0 | 10110 | 2 | 0 | 0 | 0 | 0 | 2 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0036 | 0/0 | 10108 | 2 | 0 | 2 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0037 | 0/0 | 10108 | 2 | 0 | 0 | 0 | 2 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0038 | 0/0 | 10109 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0040 | 0/0 | 10108 | 2 | 0 | 2 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0042 | 0/0 | 10108 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0043 | 0/0 | 10110 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0044 | 0/0 | 10111 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0045 | 0/0 | 10108 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0047 | 0/0 | 10111 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0065 | 0/0 | 10108 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0066 | 0/0 | 10107 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0067 | 0/0 | 10110 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0068 | 0/0 | 10109 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0069 | 0/0 | 10111 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0071 | 0/0 | 10109 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0072 | 0/0 | 10109 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0073 | 0/0 | 10109 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0074 | 0/0 | 10109 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0075 | 0/0 | 10109 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0076 | 0/0 | 10111 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0077 | 0/0 | 10111 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0078 | 0/0 | 10110 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0080 | 0/0 | 10108 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0081 | 0/0 | 10107 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0082 | 0/0 | 10108 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0083 | 0/0 | 10108 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0084 | 0/0 | 10108 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0085 | 0/0 | 10108 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0086 | 0/0 | 10108 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0087 | 0/0 | 10109 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0088 | 0/0 | 10108 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0089 | 0/0 | 10108 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0090 | 0/0 | 10108 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0091 | 0/0 | 10108 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0092 | 0/0 | 10108 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0093 | 0/0 | 10109 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0094 | 0/0 | 10108 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0095 | 0/0 | 10109 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0096 | 0/0 | 10108 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0097 | 0/0 | 10109 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0098 | 0/0 | 10108 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0099 | 0/0 | 10109 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0100 | 0/0 | 10108 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0101 | 0/0 | 10108 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0104 | 0/0 | 10110 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0105 | 0/0 | 10109 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0107 | 0/0 | 10111 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0109 | 0/0 | 10112 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0110 | 0/0 | 10109 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0111 | 0/0 | 10109 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0112 | 0/0 | 10110 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0001t0113 | 0/0 | 10110 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0002 | 0/0 | 10110 | 39 | 6 | 15 | 13 | 2 | 3 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0008 | 0/0 | 10112 | 9 | 0 | 2 | 7 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0009 | 0/0 | 10111 | 5 | 0 | 0 | 5 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0014 | 0/0 | 10110 | 4 | 0 | 0 | 4 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0025 | 0/0 | 10110 | 2 | 1 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0026 | 0/0 | 10110 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0027 | 0/0 | 10111 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0028 | 0/0 | 10111 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0039 | 1/0 | 10110 | 2 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0041 | 0/0 | 10110 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0048 | 0/0 | 10110 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0049 | 0/0 | 10110 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0050 | 0/0 | 10110 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0051 | 0/0 | 10111 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0052 | 0/0 | 10109 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0053 | 0/0 | 10111 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0054 | 0/0 | 10109 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0056 | 0/0 | 10111 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0057 | 0/0 | 10111 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0058 | 0/0 | 10112 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0059 | 0/0 | 10112 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0061 | 0/0 | 10113 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0063 | 0/0 | 10110 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0064 | 0/0 | 10110 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0102 | 0/0 | 10110 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0103 | 0/0 | 10110 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0106 | 0/0 | 10110 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0002t0114 | 0/0 | 10110 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0003t0005 | 0/0 | 10108 | 9 | 9 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0004t0019 | 0/0 | 10104 | 3 | 2 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0004t0046 | 0/0 | 10110 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0004t0060 | 0/0 | 10105 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0004t0062 | 0/0 | 10105 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0005t0004 | 0/0 | 10109 | 3 | 0 | 0 | 3 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0006t0035 | 0/0 | 10108 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0006t0079 | 0/0 | 10109 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0007t0055 | 0/0 | 10109 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0008t0108 | 0/0 | 10113 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0009t0021 | 0/0 | 10108 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0010t0070 | 0/0 | 10110 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
a0001c0011t0001 | 0/0 | 10108 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | copy fasta | chr5 | 112971798 | 113027195 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0283 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0004g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0004g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0010g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0010g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0010g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0010g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0011g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0011g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0011g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0011g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0011g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0012g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0012g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0012g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0012g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0013g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0013g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0013g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0013g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0013g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0015g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0015g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0015g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0015g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0016g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0016g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0016g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0016g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0017g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0017g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0017g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0018g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0018g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0018g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0018g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0020g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0020g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0020g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0021g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0021g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0022g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0022g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0022g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0023g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0023g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0023g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0024g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0024g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0024g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0029g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0029g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0030g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0030g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0031g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0031g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0032g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0033g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0033g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0034g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0034g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0036g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0036g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0037g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0038g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0038g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0040g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0040g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0042g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0043g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0044g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0045g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0047g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0065g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0066g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0067g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0068g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0069g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0071g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0072g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0073g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0074g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0075g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0076g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0077g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0078g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0080g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0081g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0082g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0083g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0084g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0085g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0086g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0087g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0088g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0089g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0090g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0091g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0092g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0093g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0094g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0095g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0096g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0097g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0098g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0099g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0100g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0101g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0104g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0105g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0107g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0109g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0110g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0111g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0112g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0113g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0008g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0008g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0008g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0008g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0008g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0008g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0008g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0008g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0008g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0009g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0009g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0009g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0009g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0014g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0014g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0014g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0025g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0025g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0026g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0026g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0027g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0027g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0028g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0028g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0039g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0039g0231 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0041g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0048g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0049g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0050g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0051g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0052g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0053g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0054g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0056g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0057g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0058g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0059g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0061g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0063g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0064g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0102g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0103g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0106g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0114g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0003t0005g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0003t0005g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0003t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0003t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0003t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0003t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0003t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0004t0019g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0004t0019g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0004t0019g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0004t0046g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0004t0060g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0004t0062g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0005t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0005t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0005t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0006t0035g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0006t0035g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0006t0079g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0007t0055g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0008t0108g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0009t0021g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0010t0070g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0011t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0094 | g0224 | EUR | GBR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | GBR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00280 | hp1 | a0001 | c0001 | t0082 | g0292 | EUR | FIN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00280 | hp2 | a0001 | c0002 | t0002 | g0105 | EUR | FIN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00408 | hp1 | a0001 | c0002 | t0014 | g0005 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00423 | hp1 | a0001 | c0001 | t0010 | g0015 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00423 | hp2 | a0001 | c0002 | t0008 | g0081 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00609 | hp1 | a0001 | c0001 | t0007 | g0039 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0078 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00621 | hp1 | a0001 | c0002 | t0058 | g0079 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00621 | hp2 | a0001 | c0001 | t0093 | g0242 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0063 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00639 | hp2 | a0001 | c0002 | t0025 | g0056 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00733 | hp2 | a0001 | c0002 | t0002 | g0115 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00735 | hp1 | a0001 | c0002 | t0041 | g0101 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0264 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0116 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00741 | hp1 | a0001 | c0004 | t0019 | g0133 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01070 | hp1 | a0001 | c0001 | t0040 | g0334 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01070 | hp2 | a0001 | c0001 | t0091 | g0222 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01071 | hp1 | a0001 | c0001 | t0036 | g0248 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01071 | hp2 | a0001 | c0001 | t0040 | g0333 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01074 | hp2 | a0001 | c0001 | t0012 | g0008 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0218 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01099 | hp1 | a0001 | c0001 | t0090 | g0329 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0065 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0189 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0099 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0268 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01192 | hp2 | a0001 | c0001 | t0096 | g0267 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01243 | hp1 | a0001 | c0002 | t0102 | g0150 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01256 | hp1 | a0001 | c0001 | t0021 | g0299 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01256 | hp2 | a0001 | c0001 | t0047 | g0117 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01258 | hp1 | a0001 | c0001 | t0021 | g0300 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01261 | hp2 | a0001 | c0011 | t0001 | g0311 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0046 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0059 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01358 | hp1 | a0001 | c0001 | t0045 | g0067 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0060 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0071 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0323 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01496 | hp1 | a0001 | c0001 | t0072 | g0342 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01496 | hp2 | a0001 | c0001 | t0013 | g0153 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0190 | EUR | IBS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01515 | hp2 | a0001 | c0001 | t0016 | g0241 | EUR | IBS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0210 | EUR | IBS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01516 | hp2 | a0001 | c0001 | t0037 | g0004 | EUR | IBS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01517 | hp1 | a0001 | c0001 | t0016 | g0313 | EUR | IBS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01517 | hp2 | a0001 | c0001 | t0037 | g0004 | EUR | IBS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01884 | hp1 | a0001 | c0003 | t0005 | g0006 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01884 | hp2 | a0001 | c0001 | t0109 | g0229 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01891 | hp1 | a0001 | c0004 | t0019 | g0134 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01891 | hp2 | a0001 | c0001 | t0012 | g0167 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01928 | hp1 | a0001 | c0002 | t0008 | g0055 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01934 | hp2 | a0001 | c0001 | t0036 | g0258 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01943 | hp1 | a0001 | c0002 | t0008 | g0080 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0076 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01978 | hp2 | a0001 | c0001 | t0110 | g0332 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0109 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02015 | hp1 | a0001 | c0001 | t0075 | g0188 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02027 | hp1 | a0001 | c0001 | t0010 | g0014 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0136 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02055 | hp1 | a0001 | c0004 | t0060 | g0131 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02055 | hp2 | a0001 | c0001 | t0113 | g0156 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02074 | hp2 | a0001 | c0002 | t0051 | g0093 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02129 | hp1 | a0001 | c0001 | t0007 | g0038 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02129 | hp2 | a0001 | c0004 | t0046 | g0103 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02135 | hp2 | a0001 | c0002 | t0009 | g0085 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02145 | hp1 | a0001 | c0003 | t0005 | g0122 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0180 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02155 | hp1 | a0001 | c0002 | t0014 | g0107 | EAS | CDX | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02155 | hp2 | a0001 | c0001 | t0006 | g0138 | EAS | CDX | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0057 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02257 | hp2 | a0001 | c0001 | t0015 | g0024 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02258 | hp1 | a0001 | c0001 | t0011 | g0164 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02258 | hp2 | a0001 | c0001 | t0023 | g0010 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02280 | hp1 | a0001 | c0001 | t0100 | g0212 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02280 | hp2 | a0001 | c0001 | t0105 | g0151 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0061 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0083 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02300 | hp1 | a0001 | c0001 | t0073 | g0181 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02451 | hp1 | a0001 | c0001 | t0012 | g0008 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02451 | hp2 | a0001 | c0010 | t0070 | g0043 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02523 | hp1 | a0001 | c0002 | t0027 | g0050 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02523 | hp2 | a0001 | c0001 | t0007 | g0018 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02572 | hp1 | a0001 | c0003 | t0005 | g0007 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02572 | hp2 | a0001 | c0001 | t0018 | g0330 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0184 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02602 | hp2 | a0001 | c0002 | t0002 | g0112 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02615 | hp1 | a0001 | c0003 | t0005 | g0006 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02615 | hp2 | a0001 | c0002 | t0057 | g0092 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02622 | hp1 | a0001 | c0001 | t0011 | g0165 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02622 | hp2 | a0001 | c0001 | t0018 | g0312 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02630 | hp1 | a0001 | c0001 | t0018 | g0331 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02630 | hp2 | a0001 | c0001 | t0038 | g0161 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02647 | hp1 | a0001 | c0002 | t0048 | g0052 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02647 | hp2 | a0001 | c0001 | t0029 | g0030 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0111 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02683 | hp2 | a0001 | c0001 | t0086 | g0221 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02717 | hp2 | a0001 | c0003 | t0005 | g0121 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02723 | hp1 | a0001 | c0003 | t0005 | g0119 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02723 | hp2 | a0001 | c0001 | t0084 | g0142 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02735 | hp1 | a0001 | c0001 | t0081 | g0233 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02738 | hp2 | a0001 | c0001 | t0077 | g0179 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02809 | hp1 | a0001 | c0001 | t0023 | g0211 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02809 | hp2 | a0001 | c0001 | t0013 | g0157 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02818 | hp1 | a0001 | c0001 | t0071 | g0028 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02818 | hp2 | a0001 | c0001 | t0023 | g0213 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02886 | hp1 | a0001 | c0001 | t0022 | g0216 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02886 | hp2 | a0001 | c0001 | t0013 | g0154 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02895 | hp1 | a0001 | c0001 | t0022 | g0217 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02895 | hp2 | a0001 | c0002 | t0054 | g0049 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02896 | hp1 | a0001 | c0001 | t0024 | g0202 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02896 | hp2 | a0001 | c0001 | t0011 | g0163 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02897 | hp1 | a0001 | c0001 | t0022 | g0215 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02897 | hp2 | a0001 | c0001 | t0024 | g0201 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02922 | hp1 | a0001 | c0007 | t0055 | g0047 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0162 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0100 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02970 | hp2 | a0001 | c0001 | t0030 | g0123 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02976 | hp1 | a0001 | c0001 | t0017 | g0214 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02976 | hp2 | a0001 | c0002 | t0052 | g0048 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03041 | hp1 | a0001 | c0001 | t0015 | g0025 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0054 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03098 | hp2 | a0001 | c0001 | t0012 | g0148 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03130 | hp1 | a0001 | c0001 | t0029 | g0029 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03130 | hp2 | a0001 | c0008 | t0108 | g0236 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03195 | hp1 | a0001 | c0001 | t0015 | g0026 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03195 | hp2 | a0001 | c0004 | t0062 | g0132 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03209 | hp1 | a0001 | c0001 | t0013 | g0155 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03209 | hp2 | a0001 | c0001 | t0067 | g0042 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03225 | hp1 | a0001 | c0001 | t0112 | g0128 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03225 | hp2 | a0001 | c0001 | t0011 | g0159 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03453 | hp1 | a0001 | c0003 | t0005 | g0120 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03453 | hp2 | a0001 | c0001 | t0069 | g0040 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03486 | hp1 | a0001 | c0002 | t0103 | g0149 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03486 | hp2 | a0001 | c0004 | t0019 | g0020 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0174 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03491 | hp2 | a0001 | c0001 | t0032 | g0009 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03492 | hp1 | a0001 | c0001 | t0032 | g0009 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0175 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03516 | hp1 | a0001 | c0001 | t0024 | g0166 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03516 | hp2 | a0001 | c0001 | t0011 | g0160 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0219 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03540 | hp2 | a0001 | c0003 | t0005 | g0118 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03579 | hp1 | a0001 | c0001 | t0038 | g0023 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03669 | hp1 | a0001 | c0001 | t0034 | g0182 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0051 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03831 | hp1 | a0001 | c0001 | t0078 | g0187 | SAS | BEB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | BEB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03834 | hp1 | a0001 | c0009 | t0021 | g0240 | SAS | BEB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03834 | hp2 | a0001 | c0001 | t0074 | g0170 | SAS | BEB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03927 | hp1 | a0001 | c0002 | t0114 | g0223 | SAS | BEB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | BEB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03942 | hp1 | a0001 | c0001 | t0083 | g0291 | SAS | BEB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0337 | SAS | BEB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG04115 | hp1 | a0001 | c0001 | t0080 | g0019 | SAS | STU | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0171 | SAS | STU | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG04199 | hp1 | a0001 | c0001 | t0034 | g0183 | SAS | STU | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG04199 | hp2 | a0001 | c0002 | t0049 | g0110 | SAS | STU | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18522 | hp1 | a0001 | c0001 | t0015 | g0027 | AFR | YRI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | YRI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18612 | hp1 | a0001 | c0002 | t0056 | g0113 | EAS | CHB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18747 | hp1 | a0001 | c0001 | t0006 | g0197 | EAS | CHB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18747 | hp2 | a0001 | c0002 | t0009 | g0077 | EAS | CHB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0075 | AFR | YRI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18906 | hp2 | a0001 | c0001 | t0018 | g0228 | AFR | YRI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18940 | hp1 | a0001 | c0002 | t0064 | g0104 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18942 | hp1 | a0001 | c0001 | t0020 | g0003 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18942 | hp2 | a0001 | c0002 | t0008 | g0096 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18943 | hp1 | a0001 | c0001 | t0088 | g0013 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18943 | hp2 | a0001 | c0001 | t0043 | g0195 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18947 | hp1 | a0001 | c0001 | t0065 | g0044 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18947 | hp2 | a0001 | c0002 | t0026 | g0073 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18948 | hp1 | a0001 | c0001 | t0042 | g0139 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18950 | hp1 | a0001 | c0001 | t0007 | g0035 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18952 | hp1 | a0001 | c0001 | t0006 | g0140 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18952 | hp2 | a0001 | c0001 | t0033 | g0194 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18957 | hp2 | a0001 | c0001 | t0007 | g0033 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18960 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18960 | hp2 | a0001 | c0001 | t0006 | g0200 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18963 | hp1 | a0001 | c0001 | t0031 | g0206 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18965 | hp1 | a0001 | c0002 | t0026 | g0074 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18966 | hp2 | a0001 | c0001 | t0099 | g0246 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18968 | hp1 | a0001 | c0002 | t0059 | g0091 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18968 | hp2 | a0001 | c0001 | t0006 | g0141 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18970 | hp1 | a0001 | c0001 | t0006 | g0137 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18972 | hp1 | a0001 | c0002 | t0053 | g0090 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18973 | hp2 | a0001 | c0002 | t0008 | g0082 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18974 | hp1 | a0001 | c0001 | t0010 | g0304 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18975 | hp2 | a0001 | c0001 | t0020 | g0245 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18977 | hp2 | a0001 | c0001 | t0089 | g0301 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18981 | hp2 | a0001 | c0002 | t0027 | g0072 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18984 | hp1 | a0001 | c0001 | t0016 | g0259 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18984 | hp2 | a0001 | c0001 | t0016 | g0274 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18985 | hp1 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18986 | hp1 | a0001 | c0002 | t0106 | g0297 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18987 | hp1 | a0001 | c0002 | t0008 | g0053 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18987 | hp2 | a0001 | c0001 | t0087 | g0013 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18989 | hp1 | a0001 | c0002 | t0009 | g0069 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18989 | hp2 | a0001 | c0001 | t0010 | g0015 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18990 | hp2 | a0001 | c0002 | t0063 | g0102 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18992 | hp1 | a0001 | c0001 | t0068 | g0037 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18992 | hp2 | a0001 | c0005 | t0004 | g0338 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18995 | hp2 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18999 | hp1 | a0001 | c0002 | t0008 | g0068 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19000 | hp2 | a0001 | c0001 | t0010 | g0302 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19001 | hp1 | a0001 | c0001 | t0066 | g0036 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19002 | hp2 | a0001 | c0001 | t0007 | g0031 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19004 | hp1 | a0001 | c0001 | t0097 | g0234 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19004 | hp2 | a0001 | c0002 | t0008 | g0095 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19006 | hp1 | a0001 | c0002 | t0061 | g0097 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19007 | hp1 | a0001 | c0006 | t0035 | g0317 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19009 | hp2 | a0001 | c0001 | t0006 | g0199 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19010 | hp1 | a0001 | c0001 | t0076 | g0186 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19011 | hp1 | a0001 | c0002 | t0008 | g0130 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19030 | hp1 | a0001 | c0001 | t0107 | g0126 | AFR | LWK | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19030 | hp2 | a0001 | c0001 | t0017 | g0011 | AFR | LWK | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | LWK | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0066 | AFR | LWK | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19054 | hp1 | a0001 | c0001 | t0033 | g0209 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19055 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19057 | hp1 | a0001 | c0001 | t0007 | g0045 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19058 | hp1 | a0001 | c0005 | t0004 | g0319 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19058 | hp2 | a0001 | c0001 | t0031 | g0205 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19060 | hp1 | a0001 | c0002 | t0014 | g0106 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19063 | hp2 | a0001 | c0006 | t0079 | g0290 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19065 | hp1 | a0001 | c0002 | t0014 | g0005 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19065 | hp2 | a0001 | c0001 | t0007 | g0032 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19066 | hp2 | a0001 | c0001 | t0006 | g0196 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19074 | hp1 | a0001 | c0002 | t0028 | g0125 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19074 | hp2 | a0001 | c0001 | t0006 | g0198 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19077 | hp1 | a0001 | c0002 | t0028 | g0135 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19078 | hp1 | a0001 | c0006 | t0035 | g0340 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19078 | hp2 | a0001 | c0002 | t0009 | g0086 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19079 | hp2 | a0001 | c0001 | t0092 | g0220 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19080 | hp1 | a0001 | c0001 | t0098 | g0260 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19082 | hp2 | a0001 | c0001 | t0085 | g0307 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19083 | hp2 | a0001 | c0002 | t0009 | g0087 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19085 | hp1 | a0001 | c0001 | t0007 | g0034 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19087 | hp1 | a0001 | c0001 | t0044 | g0143 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19087 | hp2 | a0001 | c0005 | t0004 | g0275 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19240 | hp1 | a0001 | c0003 | t0005 | g0007 | AFR | YRI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19240 | hp2 | a0001 | c0001 | t0013 | g0147 | AFR | YRI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20129 | hp1 | a0001 | c0001 | t0104 | g0158 | AFR | ASW | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20129 | hp2 | a0001 | c0001 | t0101 | g0341 | AFR | ASW | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20752 | hp1 | a0001 | c0002 | t0050 | g0064 | EUR | TSI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0322 | EUR | TSI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0185 | EUR | TSI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0278 | EUR | TSI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0169 | SAS | GIH | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20905 | hp2 | a0001 | c0001 | t0006 | g0114 | SAS | GIH | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02109 | hp1 | a0001 | c0002 | t0039 | g0225 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02109 | hp2 | a0001 | c0001 | t0095 | g0266 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02486 | hp1 | a0001 | c0001 | t0017 | g0011 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02486 | hp2 | a0001 | c0001 | t0012 | g0168 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0098 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02559 | hp2 | a0001 | c0001 | t0017 | g0010 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03471 | hp2 | a0001 | c0001 | t0111 | g0152 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG06807 | hp1 | a0001 | c0002 | t0025 | g0129 | AFR | USA | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | USA | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18955 | hp1 | a0001 | c0001 | t0020 | g0279 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20300 | hp1 | a0001 | c0001 | t0030 | g0124 | AFR | USA | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | USA | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA21309 | hp1 | a0001 | c0001 | t0007 | g0041 | AFR | LWK | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0127 | AFR | LWK | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0283 | REF | REF | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0039 | g0231 | REF | REF | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:113022192 | AC | A | 1 | a0001 | 3 | HG02895.hp2 HG02922.hp1 HG02976.hp2 |
splice_region_variant | LOW | c.*8709delC | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | chr5 | 113022192 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:112992137 | G | T | 1 | a0001c0011 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.222G>T | p.Pro74Pro | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 3/11 | 358/10110 | 222/1263 | 74/420 | chr5 | 112992137 | ||
chr5:112992215 | T | C | 1 | a0001c0003 | 9 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(6): Show |
synonymous_variant | LOW | c.300T>C | p.Tyr100Tyr | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 3/11 | 436/10110 | 300/1263 | 100/420 | chr5 | 112992215 | ||
chr5:112992680 | A | G | 8 | a0001c0001a0001c0003a0001c0005others(5): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
synonymous_variant | LOW | c.342A>G | p.Leu114Leu | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/11 | 478/10110 | 342/1263 | 114/420 | chr5 | 112992680 | ||
chr5:113001101 | T | C | 1 | a0001c0008 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.450T>C | p.Gly150Gly | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 5/11 | 586/10110 | 450/1263 | 150/420 | chr5 | 113001101 | ||
chr5:113001206 | A | G | 1 | a0001c0007 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.555A>G | p.Lys185Lys | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 5/11 | 691/10110 | 555/1263 | 185/420 | chr5 | 113001206 | ||
chr5:113001233 | T | A | 1 | a0001c0005 | 3 | NA18992.hp2 NA19058.hp1 NA19087.hp2 |
synonymous_variant | LOW | c.582T>A | p.Ile194Ile | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 5/11 | 718/10110 | 582/1263 | 194/420 | chr5 | 113001233 | ||
chr5:113001624 | A | G | 1 | a0001c0010 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.756A>G | p.Gly252Gly | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/11 | 892/10110 | 756/1263 | 252/420 | chr5 | 113001624 | ||
chr5:113013373 | T | C | 9 | a0001c0001a0001c0003a0001c0004others(6): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
synonymous_variant | LOW | c.1152T>C | p.Ala384Ala | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1288/10110 | 1152/1263 | 384/420 | chr5 | 113013373 | ||
chr5:113013397 | T | C | 1 | a0001c0006 | 3 | NA19007.hp1 NA19063.hp2 NA19078.hp1 |
synonymous_variant | LOW | c.1176T>C | p.Asn392Asn | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1312/10110 | 1176/1263 | 392/420 | chr5 | 113013397 | ||
chr5:113013412 | C | T | 1 | a0001c0009 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.1191C>T | p.Phe397Phe | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1327/10110 | 1191/1263 | 397/420 | chr5 | 113013412 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:112976805 | C | A | 1 | a0001c0002t0041 | 1 | HG00735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-129C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/11 | 129 | chr5 | 112976805 | |||||
chr5:112976831 | T | C | 34 | a0001c0001t0006a0001c0001t0042a0001c0001t0043others(31): Show | 103 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(100): Show |
5_prime_UTR_variant | MODIFIER | c.-103T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/11 | 103 | chr5 | 112976831 | |||||
chr5:112976883 | T | C | 8 | a0001c0001t0007a0001c0001t0029a0001c0001t0065others(5): Show | 18 | HG00609.hp1 HG02129.hp1 HG02451.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-51T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/11 | 51 | chr5 | 112976883 | |||||
chr5:113013597 | G | A | 4 | a0001c0001t0015a0001c0001t0030a0001c0001t0071others(1): Show | 8 | HG01496.hp1 HG02257.hp2 HG02818.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*113G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 113 | chr5 | 113013597 | |||||
chr5:113013600 | T | C | 15 | a0001c0001t0003a0001c0001t0006a0001c0001t0031others(12): Show | 52 | HG01106.hp1 HG01515.hp1 HG02015.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*116T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 116 | chr5 | 113013600 | |||||
chr5:113013682 | T | C | 35 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(32): Show | 134 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*198T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 198 | chr5 | 113013682 | |||||
chr5:113013682 | T | G | 1 | a0001c0001t0099 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*198T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 198 | chr5 | 113013682 | |||||
chr5:113013710 | T | C | 5 | a0001c0001t0015a0001c0001t0030a0001c0001t0038others(2): Show | 10 | HG01496.hp1 HG02257.hp2 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*226T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 226 | chr5 | 113013710 | |||||
chr5:113013953 | A | G | 1 | a0001c0002t0064 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*469A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 469 | chr5 | 113013953 | |||||
chr5:113013980 | T | A | 1 | a0001c0002t0025 | 2 | HG00639.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*496T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 496 | chr5 | 113013980 | |||||
chr5:113013993 | T | G | 1 | a0001c0001t0022 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*509T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 509 | chr5 | 113013993 | |||||
chr5:113014000 | C | G | 1 | a0001c0002t0114 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*516C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 516 | chr5 | 113014000 | |||||
chr5:113014084 | G | A | 1 | a0001c0001t0100 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*600G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 600 | chr5 | 113014084 | |||||
chr5:113014157 | G | A | 2 | a0001c0006t0035a0001c0006t0079 | 3 | NA19007.hp1 NA19063.hp2 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*673G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 673 | chr5 | 113014157 | |||||
chr5:113014158 | G | T | 1 | a0001c0010t0070 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*674G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 674 | chr5 | 113014158 | |||||
chr5:113014333 | G | A | 1 | a0001c0001t0101 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*849G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 849 | chr5 | 113014333 | |||||
chr5:113014370 | C | T | 1 | a0001c0001t0030 | 2 | HG02970.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*886C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 886 | chr5 | 113014370 | |||||
chr5:113014401 | C | T | 19 | a0001c0001t0003a0001c0001t0006a0001c0001t0013others(16): Show | 60 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*917C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 917 | chr5 | 113014401 | |||||
chr5:113014474 | A | C | 1 | a0001c0002t0063 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*990A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 990 | chr5 | 113014474 | |||||
chr5:113014609 | T | A | 1 | a0001c0001t0073 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1125T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1125 | chr5 | 113014609 | |||||
chr5:113014632 | G | C | 1 | a0001c0001t0111 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1148G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1148 | chr5 | 113014632 | |||||
chr5:113014677 | G | C | 2 | a0001c0002t0048a0001c0002t0102 | 2 | HG01243.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1193G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1193 | chr5 | 113014677 | |||||
chr5:113014758 | A | ATG | 1 | a0001c0001t0012 | 5 | HG01074.hp2 HG01891.hp2 HG02451.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1286_*1287dupGT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1288 | INFO_REALIGN_3_PRIME | chr5 | 113014758 | ||||
chr5:113014838 | A | C | 1 | a0001c0010t0070 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1354A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1354 | chr5 | 113014838 | |||||
chr5:113014883 | T | C | 1 | a0001c0001t0029 | 2 | HG02647.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1399T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1399 | chr5 | 113014883 | |||||
chr5:113015010 | G | A | 33 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(30): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*1526G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1526 | chr5 | 113015010 | |||||
chr5:113015177 | G | A | 1 | a0001c0001t0065 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1693G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1693 | chr5 | 113015177 | |||||
chr5:113015361 | G | GT | 4 | a0001c0001t0024a0001c0001t0044a0001c0004t0062others(1): Show | 6 | HG02896.hp1 HG02897.hp2 HG03195.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1888dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1889 | INFO_REALIGN_3_PRIME | chr5 | 113015361 | ||||
chr5:113015600 | A | G | 2 | a0001c0001t0095a0001c0001t0096 | 2 | HG01192.hp2 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2116A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 2116 | chr5 | 113015600 | |||||
chr5:113015920 | A | C | 2 | a0001c0001t0021a0001c0009t0021 | 3 | HG01256.hp1 HG01258.hp1 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2436A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 2436 | chr5 | 113015920 | |||||
chr5:113015957 | G | T | 1 | a0001c0001t0012 | 5 | HG01074.hp2 HG01891.hp2 HG02451.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2473G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 2473 | chr5 | 113015957 | |||||
chr5:113016187 | G | C | 1 | a0001c0002t0049 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2703G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 2703 | chr5 | 113016187 | |||||
chr5:113016188 | G | T | 1 | a0001c0001t0094 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2704G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 2704 | chr5 | 113016188 | |||||
chr5:113016310 | C | G | 1 | a0001c0001t0010 | 5 | HG00423.hp1 HG02027.hp1 NA18974.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2826C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 2826 | chr5 | 113016310 | |||||
chr5:113016350 | A | G | 1 | a0001c0010t0070 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2866A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 2866 | chr5 | 113016350 | |||||
chr5:113016464 | T | C | 1 | a0001c0010t0070 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2980T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 2980 | chr5 | 113016464 | |||||
chr5:113016531 | G | A | 1 | a0001c0001t0022 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3047G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3047 | chr5 | 113016531 | |||||
chr5:113016572 | G | A | 1 | a0001c0001t0022 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3088G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3088 | chr5 | 113016572 | |||||
chr5:113016594 | C | A | 1 | a0001c0002t0049 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3110C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3110 | chr5 | 113016594 | |||||
chr5:113016840 | C | CT | 72 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(69): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*3374dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3375 | INFO_REALIGN_3_PRIME | chr5 | 113016840 | ||||
chr5:113016840 | C | CTT | 9 | a0001c0001t0012a0001c0001t0016a0001c0001t0034others(6): Show | 17 | HG00621.hp2 HG01074.hp2 HG01515.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3373_*3374dupTT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3375 | INFO_REALIGN_3_PRIME | chr5 | 113016840 | ||||
chr5:113016919 | G | T | 1 | a0001c0007t0055 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3435G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3435 | chr5 | 113016919 | |||||
chr5:113016947 | T | C | 1 | a0001c0001t0111 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3463T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3463 | chr5 | 113016947 | |||||
chr5:113016966 | C | G | 1 | a0001c0001t0037 | 2 | HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3482C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3482 | chr5 | 113016966 | |||||
chr5:113016968 | A | G | 1 | a0001c0001t0112 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3484A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3484 | chr5 | 113016968 | |||||
chr5:113017047 | G | C | 1 | a0001c0001t0065 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3563G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3563 | chr5 | 113017047 | |||||
chr5:113017096 | C | G | 1 | a0001c0001t0112 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3612C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3612 | chr5 | 113017096 | |||||
chr5:113017133 | T | C | 1 | a0001c0002t0056 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3649T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3649 | chr5 | 113017133 | |||||
chr5:113017169 | G | T | 1 | a0001c0001t0112 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3685G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3685 | chr5 | 113017169 | |||||
chr5:113017304 | CTG | C | 11 | a0001c0001t0007a0001c0001t0029a0001c0001t0040others(8): Show | 24 | HG00609.hp1 HG00741.hp1 HG01070.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3822_*3823delGT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3822 | INFO_REALIGN_3_PRIME | chr5 | 113017304 | ||||
chr5:113017346 | G | A | 1 | a0001c0001t0082 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3862G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3862 | chr5 | 113017346 | |||||
chr5:113017408 | T | G | 4 | a0001c0001t0017a0001c0001t0023a0001c0001t0100others(1): Show | 9 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3924T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3924 | chr5 | 113017408 | |||||
chr5:113017411 | G | T | 1 | a0001c0001t0097 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3927G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3927 | chr5 | 113017411 | |||||
chr5:113017627 | G | T | 5 | a0001c0001t0015a0001c0001t0030a0001c0001t0038others(2): Show | 10 | HG01496.hp1 HG02257.hp2 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4143G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 4143 | chr5 | 113017627 | |||||
chr5:113017752 | G | A | 2 | a0001c0002t0009a0001c0002t0058 | 6 | HG00621.hp1 HG02135.hp2 NA18747.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4268G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 4268 | chr5 | 113017752 | |||||
chr5:113017814 | A | G | 1 | a0001c0001t0011 | 5 | HG02258.hp1 HG02622.hp1 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4330A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 4330 | chr5 | 113017814 | |||||
chr5:113017840 | C | G | 3 | a0001c0002t0014a0001c0002t0063a0001c0002t0106 | 6 | HG00408.hp1 HG02155.hp1 NA18986.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4356C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 4356 | chr5 | 113017840 | |||||
chr5:113017937 | A | G | 1 | a0001c0002t0054 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4453A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 4453 | chr5 | 113017937 | |||||
chr5:113018190 | A | C | 1 | a0001c0001t0092 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4706A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 4706 | chr5 | 113018190 | |||||
chr5:113018372 | A | T | 1 | a0001c0010t0070 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4888A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 4888 | chr5 | 113018372 | |||||
chr5:113018401 | G | A | 1 | a0001c0001t0074 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4917G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 4917 | chr5 | 113018401 | |||||
chr5:113018669 | G | A | 1 | a0001c0002t0050 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5185G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5185 | chr5 | 113018669 | |||||
chr5:113018715 | C | G | 1 | a0001c0002t0028 | 2 | NA19074.hp1 NA19077.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5231C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5231 | chr5 | 113018715 | |||||
chr5:113018720 | T | A | 10 | a0001c0001t0007a0001c0001t0029a0001c0001t0040others(7): Show | 21 | HG00609.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*5236T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5236 | chr5 | 113018720 | |||||
chr5:113018856 | G | C | 1 | a0001c0001t0040 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5372G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5372 | chr5 | 113018856 | |||||
chr5:113018857 | C | G | 1 | a0001c0002t0026 | 2 | NA18947.hp2 NA18965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5373C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5373 | chr5 | 113018857 | |||||
chr5:113018889 | G | A | 1 | a0001c0001t0093 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5405G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5405 | chr5 | 113018889 | |||||
chr5:113019126 | C | T | 1 | a0001c0001t0072 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5642C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5642 | chr5 | 113019126 | |||||
chr5:113019201 | C | G | 43 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(40): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*5717C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5717 | chr5 | 113019201 | |||||
chr5:113019313 | G | A | 1 | a0001c0001t0083 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5829G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5829 | chr5 | 113019313 | |||||
chr5:113019320 | C | G | 1 | a0001c0001t0107 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5836C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5836 | chr5 | 113019320 | |||||
chr5:113019534 | G | C | 2 | a0001c0002t0009a0001c0002t0058 | 6 | HG00621.hp1 HG02135.hp2 NA18747.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6050G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 6050 | chr5 | 113019534 | |||||
chr5:113019571 | A | G | 1 | a0001c0010t0070 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6087A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 6087 | chr5 | 113019571 | |||||
chr5:113019578 | G | C | 1 | a0001c0001t0022 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6094G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 6094 | chr5 | 113019578 | |||||
chr5:113019971 | C | G | 31 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(28): Show | 130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*6487C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 6487 | chr5 | 113019971 | |||||
chr5:113020002 | G | T | 2 | a0001c0002t0053a0001c0002t0059 | 2 | NA18968.hp1 NA18972.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6518G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 6518 | chr5 | 113020002 | |||||
chr5:113020157 | A | G | 2 | a0001c0001t0104a0001c0001t0105 | 2 | HG02280.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6673A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 6673 | chr5 | 113020157 | |||||
chr5:113020162 | A | G | 1 | a0001c0010t0070 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6678A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 6678 | chr5 | 113020162 | |||||
chr5:113020211 | A | G | 43 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(40): Show | 162 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*6727A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 6727 | chr5 | 113020211 | |||||
chr5:113020369 | CTA | C | 41 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(38): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*6888_*6889delTA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 6888 | INFO_REALIGN_3_PRIME | chr5 | 113020369 | ||||
chr5:113020609 | C | T | 1 | a0001c0001t0036 | 2 | HG01071.hp1 HG01934.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7125C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7125 | chr5 | 113020609 | |||||
chr5:113020652 | A | G | 1 | a0001c0001t0091 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7168A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7168 | chr5 | 113020652 | |||||
chr5:113020744 | A | G | 1 | a0001c0001t0090 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7260A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7260 | chr5 | 113020744 | |||||
chr5:113020763 | G | T | 1 | a0001c0001t0033 | 2 | NA18952.hp2 NA19054.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7279G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7279 | chr5 | 113020763 | |||||
chr5:113020766 | T | G | 10 | a0001c0001t0007a0001c0001t0029a0001c0001t0040others(7): Show | 21 | HG00609.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*7282T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7282 | chr5 | 113020766 | |||||
chr5:113020789 | T | G | 1 | a0001c0001t0085 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7305T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7305 | chr5 | 113020789 | |||||
chr5:113020847 | A | G | 2 | a0001c0001t0018a0001c0001t0109 | 5 | HG01884.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7363A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7363 | chr5 | 113020847 | |||||
chr5:113020952 | G | A | 41 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(38): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*7468G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7468 | chr5 | 113020952 | |||||
chr5:113021001 | C | T | 1 | a0001c0001t0078 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7517C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7517 | chr5 | 113021001 | |||||
chr5:113021042 | A | G | 3 | a0001c0001t0013a0001c0001t0111a0001c0001t0113 | 7 | HG01496.hp2 HG02055.hp2 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7558A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7558 | chr5 | 113021042 | |||||
chr5:113021087 | A | T | 1 | a0001c0001t0071 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7603A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7603 | chr5 | 113021087 | |||||
chr5:113021175 | C | G | 1 | a0001c0001t0089 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7691C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7691 | chr5 | 113021175 | |||||
chr5:113021219 | T | C | 1 | a0001c0001t0075 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7735T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7735 | chr5 | 113021219 | |||||
chr5:113021358 | ACT | A | 1 | a0001c0001t0022 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7877_*7878delCT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7877 | INFO_REALIGN_3_PRIME | chr5 | 113021358 | ||||
chr5:113021381 | A | C | 1 | a0001c0001t0078 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7897A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7897 | chr5 | 113021381 | |||||
chr5:113021386 | C | CA | 15 | a0001c0001t0004a0001c0001t0017a0001c0001t0018others(12): Show | 40 | HG00423.hp2 HG00621.hp1 HG00735.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*7920dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7921 | INFO_REALIGN_3_PRIME | chr5 | 113021386 | ||||
chr5:113021386 | CA | C | 22 | a0001c0001t0007a0001c0001t0011a0001c0001t0012others(19): Show | 51 | HG00609.hp1 HG01070.hp1 HG01071.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*7920delA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7920 | INFO_REALIGN_3_PRIME | chr5 | 113021386 | ||||
chr5:113021386 | CAA | C | 14 | a0001c0001t0003a0001c0001t0006a0001c0001t0013others(11): Show | 54 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*7919_*7920delAA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7919 | INFO_REALIGN_3_PRIME | chr5 | 113021386 | ||||
chr5:113021404 | A | C | 1 | a0001c0001t0112 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7920A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7920 | chr5 | 113021404 | |||||
chr5:113021405 | C | A | 1 | a0001c0001t0086 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7921C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7921 | chr5 | 113021405 | |||||
chr5:113021461 | TTAAG | T | 3 | a0001c0004t0019a0001c0004t0060a0001c0004t0062 | 5 | HG00741.hp1 HG01891.hp1 HG02055.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7979_*7982delAAGT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7979 | INFO_REALIGN_3_PRIME | chr5 | 113021461 | ||||
chr5:113021541 | T | TTAAG | 1 | a0001c0001t0020 | 3 | NA18942.hp1 NA18955.hp1 NA18975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8059_*8062dupAAGT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 8063 | INFO_REALIGN_3_PRIME | chr5 | 113021541 | ||||
chr5:113021599 | G | A | 1 | a0001c0001t0032 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8115G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 8115 | chr5 | 113021599 | |||||
chr5:113021646 | G | GTAAC | 3 | a0001c0001t0018a0001c0001t0109a0001c0008t0108 | 6 | HG01884.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8164_*8167dupAACT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 8168 | INFO_REALIGN_3_PRIME | chr5 | 113021646 | ||||
chr5:113021705 | AG | A | 42 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(39): Show | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*8222delG | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 8222 | chr5 | 113021705 | |||||
chr5:113021782 | A | G | 2 | a0001c0001t0087a0001c0001t0088 | 2 | NA18943.hp1 NA18987.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8298A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 8298 | chr5 | 113021782 | |||||
chr5:113022033 | T | C | 1 | a0001c0002t0103 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8549T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 8549 | chr5 | 113022033 | |||||
chr5:113022070 | G | A | 8 | a0001c0001t0007a0001c0001t0029a0001c0001t0065others(5): Show | 18 | HG00609.hp1 HG02129.hp1 HG02523.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*8586G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 8586 | chr5 | 113022070 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:112977016 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.53+30C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977016 | ||||||
chr5:112977018 | G | C | 1 | a0001c0001t0007g0018 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.53+32G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977018 | ||||||
chr5:112977028 | C | A | 1 | a0001c0001t0080g0019 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.53+42C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977028 | ||||||
chr5:112977039 | G | C | 210 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(207): Show | 218 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(215): Show |
intron_variant | MODIFIER | c.53+53G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977039 | ||||||
chr5:112977045 | C | T | 1 | a0001c0001t0005g0219 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.53+59C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977045 | ||||||
chr5:112977157 | C | T | 1 | a0001c0001t0072g0342 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.53+171C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977157 | ||||||
chr5:112977185 | C | T | 1 | a0001c0002t0002g0218 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.53+199C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977185 | ||||||
chr5:112977257 | A | T | 10 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(7): Show | 11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.53+271A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977257 | ||||||
chr5:112977292 | G | A | 1 | a0001c0004t0019g0020 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.53+306G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977292 | ||||||
chr5:112977545 | C | T | 1 | a0001c0002t0002g0210 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.53+559C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977545 | ||||||
chr5:112977636 | C | G | 1 | a0001c0001t0033g0209 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.53+650C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977636 | ||||||
chr5:112977660 | G | C | 1 | a0001c0001t0005g0219 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.53+674G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977660 | ||||||
chr5:112977761 | C | G | 6 | a0001c0001t0003g0203a0001c0001t0003g0204a0001c0001t0003g0207others(3): Show | 6 | NA18957.hp1 NA18963.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.53+775C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977761 | ||||||
chr5:112977778 | G | A | 2 | a0001c0001t0006g0022a0001c0002t0002g0021 | 2 | HG01243.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.53+792G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977778 | ||||||
chr5:112977948 | G | GT | 85 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(82): Show | 88 | HG01074.hp2 HG01106.hp1 HG01243.hp1 others(85): Show |
intron_variant | MODIFIER | c.53+968dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112977948 | |||||
chr5:112977954 | T | TG | 6 | a0001c0001t0015g0024a0001c0001t0015g0025a0001c0001t0015g0026others(3): Show | 6 | HG02257.hp2 HG02818.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.53+972dupG | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112977954 | |||||
chr5:112977978 | T | G | 5 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0140others(2): Show | 5 | HG02155.hp2 NA18948.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+992T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977978 | ||||||
chr5:112978040 | C | A | 6 | a0001c0001t0015g0024a0001c0001t0015g0025a0001c0001t0015g0026others(3): Show | 6 | HG02257.hp2 HG02818.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.53+1054C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978040 | ||||||
chr5:112978135 | C | G | 1 | a0001c0002t0002g0136 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.53+1149C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978135 | ||||||
chr5:112978274 | C | T | 80 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(77): Show | 82 | HG01074.hp2 HG01106.hp1 HG01243.hp1 others(79): Show |
intron_variant | MODIFIER | c.53+1288C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978274 | ||||||
chr5:112978341 | G | A | 1 | a0001c0001t0044g0143 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.53+1355G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978341 | ||||||
chr5:112978414 | T | C | 2 | a0001c0001t0029g0029a0001c0001t0029g0030 | 2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.53+1428T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978414 | ||||||
chr5:112978445 | A | G | 2 | a0001c0001t0024g0201a0001c0001t0024g0202 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.53+1459A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978445 | ||||||
chr5:112978498 | A | G | 1 | a0001c0001t0101g0341 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.53+1512A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978498 | ||||||
chr5:112978568 | T | G | 3 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146 | 3 | HG03471.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.53+1582T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978568 | ||||||
chr5:112978581 | A | G | 49 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(46): Show | 50 | HG01106.hp1 HG01515.hp1 HG02015.hp1 others(47): Show |
intron_variant | MODIFIER | c.53+1595A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978581 | ||||||
chr5:112978584 | A | G | 80 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(77): Show | 82 | HG01074.hp2 HG01106.hp1 HG01243.hp1 others(79): Show |
intron_variant | MODIFIER | c.53+1598A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978584 | ||||||
chr5:112978611 | T | C | 18 | a0001c0001t0007g0018a0001c0001t0007g0031a0001c0001t0007g0032others(15): Show | 18 | HG00609.hp1 HG02129.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.53+1625T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978611 | ||||||
chr5:112978683 | T | TA | 95 | a0001c0001t0006g0022a0001c0001t0006g0114a0001c0001t0030g0123others(92): Show | 100 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.53+1710dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112978683 | |||||
chr5:112978744 | C | T | 1 | a0001c0006t0035g0340 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.53+1758C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978744 | ||||||
chr5:112978751 | C | T | 6 | a0001c0001t0015g0024a0001c0001t0015g0025a0001c0001t0015g0026others(3): Show | 6 | HG02257.hp2 HG02818.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.53+1765C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978751 | ||||||
chr5:112978755 | C | T | 2 | a0001c0002t0028g0125a0001c0002t0028g0135 | 2 | NA19074.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.53+1769C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978755 | ||||||
chr5:112978756 | A | G | 102 | a0001c0001t0006g0022a0001c0001t0006g0114a0001c0001t0030g0123others(99): Show | 107 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.53+1770A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978756 | ||||||
chr5:112978757 | A | G | 3 | a0001c0001t0012g0008a0001c0001t0012g0167a0001c0001t0012g0168 | 4 | HG01074.hp2 HG01891.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.53+1771A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978757 | ||||||
chr5:112978910 | T | G | 1 | a0001c0001t0003g0169 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.53+1924T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978910 | ||||||
chr5:112978995 | A | G | 1 | a0001c0001t0001g0339 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.53+2009A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978995 | ||||||
chr5:112979015 | CTGTTAAC others(7): Show |
C | 10 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(7): Show | 11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.53+2033_53+2046del others(14): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112979015 | |||||
chr5:112979039 | C | A | 1 | a0001c0002t0002g0046 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.53+2053C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979039 | ||||||
chr5:112979073 | A | G | 10 | a0001c0001t0005g0162a0001c0001t0011g0159a0001c0001t0011g0160others(7): Show | 10 | HG02258.hp1 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.53+2087A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979073 | ||||||
chr5:112979126 | GT | G | 90 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(87): Show | 93 | HG01074.hp2 HG01106.hp1 HG01243.hp1 others(90): Show |
intron_variant | MODIFIER | c.53+2141delT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979126 | ||||||
chr5:112979334 | C | G | 9 | a0001c0001t0030g0123a0001c0001t0030g0124a0001c0003t0005g0006others(6): Show | 11 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.53+2348C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979334 | ||||||
chr5:112979469 | C | A | 1 | a0001c0001t0013g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.53+2483C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979469 | ||||||
chr5:112979516 | G | T | 1 | a0001c0001t0112g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.53+2530G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979516 | ||||||
chr5:112979718 | G | A | 1 | a0001c0007t0055g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.53+2732G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979718 | ||||||
chr5:112979786 | A | G | 11 | a0001c0001t0006g0138a0001c0001t0006g0140a0001c0001t0006g0141others(8): Show | 11 | HG02155.hp2 NA18747.hp1 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.53+2800A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979786 | ||||||
chr5:112979852 | T | A | 3 | a0001c0002t0052g0048a0001c0002t0054g0049a0001c0007t0055g0047 | 3 | HG02895.hp2 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.53+2866T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979852 | ||||||
chr5:112979935 | C | T | 1 | a0001c0001t0006g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.53+2949C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979935 | ||||||
chr5:112980005 | G | A | 2 | a0001c0001t0029g0029a0001c0001t0029g0030 | 2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.53+3019G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980005 | ||||||
chr5:112980062 | T | A | 2 | a0001c0001t0007g0031a0001c0001t0007g0032 | 2 | NA19002.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.53+3076T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980062 | ||||||
chr5:112980156 | G | A | 176 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(173): Show | 182 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.53+3170G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980156 | ||||||
chr5:112980165 | A | G | 3 | a0001c0001t0024g0166a0001c0001t0024g0201a0001c0001t0024g0202 | 3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.53+3179A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980165 | ||||||
chr5:112980231 | A | G | 1 | a0001c0005t0004g0338 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.53+3245A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980231 | ||||||
chr5:112980317 | C | G | 1 | a0001c0001t0013g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.53+3331C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980317 | ||||||
chr5:112980553 | A | G | 1 | a0001c0001t0071g0028 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.53+3567A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980553 | ||||||
chr5:112980585 | A | AC | 176 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(173): Show | 182 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.53+3600dupC | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112980585 | |||||
chr5:112980620 | C | A | 1 | a0001c0002t0027g0050 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.53+3634C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980620 | ||||||
chr5:112980645 | A | G | 2 | a0001c0001t0007g0045a0001c0001t0065g0044 | 2 | NA18947.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.53+3659A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980645 | ||||||
chr5:112980779 | A | C | 2 | a0001c0002t0002g0115a0001c0002t0002g0116 | 2 | HG00733.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.53+3793A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980779 | ||||||
chr5:112980879 | A | G | 1 | a0001c0001t0001g0337 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.53+3893A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980879 | ||||||
chr5:112981029 | A | AT | 93 | a0001c0001t0006g0022a0001c0001t0006g0114a0001c0001t0045g0067others(90): Show | 96 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.53+4053dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112981029 | |||||
chr5:112981212 | C | T | 1 | a0001c0001t0006g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.53+4226C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112981212 | ||||||
chr5:112981223 | C | G | 9 | a0001c0001t0030g0123a0001c0001t0030g0124a0001c0003t0005g0006others(6): Show | 11 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.53+4237C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112981223 | ||||||
chr5:112981230 | G | A | 12 | a0001c0001t0007g0018a0001c0001t0007g0031a0001c0001t0007g0032others(9): Show | 12 | HG00609.hp1 HG02129.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.53+4244G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112981230 | ||||||
chr5:112981232 | A | G | 1 | a0001c0001t0044g0143 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.53+4246A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112981232 | ||||||
chr5:112981350 | G | A | 10 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(7): Show | 11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.53+4364G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112981350 | ||||||
chr5:112981668 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.54-4167G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112981668 | ||||||
chr5:112981720 | T | C | 116 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(113): Show | 121 | HG00609.hp1 HG01074.hp2 HG01106.hp1 others(118): Show |
intron_variant | MODIFIER | c.54-4115T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112981720 | ||||||
chr5:112981733 | T | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0227 | 4 | NA18940.hp2 NA19070.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-4102T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112981733 | ||||||
chr5:112982033 | G | A | 1 | a0001c0002t0028g0135 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.54-3802G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982033 | ||||||
chr5:112982069 | C | T | 3 | a0001c0002t0052g0048a0001c0002t0054g0049a0001c0007t0055g0047 | 3 | HG02895.hp2 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.54-3766C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982069 | ||||||
chr5:112982087 | A | G | 1 | a0001c0002t0056g0113 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.54-3748A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982087 | ||||||
chr5:112982137 | T | G | 1 | a0001c0001t0112g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.54-3698T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982137 | ||||||
chr5:112982175 | A | G | 14 | a0001c0001t0007g0018a0001c0001t0007g0031a0001c0001t0007g0032others(11): Show | 14 | HG00609.hp1 HG02129.hp1 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.54-3660A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982175 | ||||||
chr5:112982191 | T | TTA | 116 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(113): Show | 121 | HG00609.hp1 HG01074.hp2 HG01106.hp1 others(118): Show |
intron_variant | MODIFIER | c.54-3644_54-3643ins others(2): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982191 | ||||||
chr5:112982233 | C | T | 2 | a0001c0001t0001g0336a0001c0002t0002g0112 | 2 | HG02602.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.54-3602C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982233 | ||||||
chr5:112982287 | A | T | 82 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(79): Show | 85 | HG00609.hp1 HG01106.hp1 HG01496.hp2 others(82): Show |
intron_variant | MODIFIER | c.54-3548A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982287 | ||||||
chr5:112982315 | C | T | 3 | a0001c0002t0002g0109a0001c0002t0002g0111a0001c0002t0049g0110 | 3 | HG01981.hp2 HG02683.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.54-3520C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982315 | ||||||
chr5:112982467 | T | A | 5 | a0001c0001t0012g0008a0001c0001t0012g0148a0001c0001t0012g0167others(2): Show | 6 | HG01074.hp2 HG01891.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.54-3368T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982467 | ||||||
chr5:112982561 | C | A | 3 | a0001c0001t0024g0166a0001c0001t0024g0201a0001c0001t0024g0202 | 3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.54-3274C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982561 | ||||||
chr5:112982598 | G | A | 1 | a0001c0001t0012g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.54-3237G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982598 | ||||||
chr5:112982624 | C | G | 2 | a0001c0001t0033g0194a0001c0001t0033g0209 | 2 | NA18952.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.54-3211C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982624 | ||||||
chr5:112982651 | GT | G | 7 | a0001c0001t0005g0162a0001c0001t0011g0159a0001c0001t0011g0160others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.54-3176delT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112982651 | |||||
chr5:112982672 | TCTTA | T | 10 | a0001c0001t0005g0162a0001c0001t0011g0159a0001c0001t0011g0160others(7): Show | 10 | HG02258.hp1 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.54-3158_54-3155del others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112982672 | |||||
chr5:112982690 | C | A | 6 | a0001c0001t0015g0024a0001c0001t0015g0025a0001c0001t0015g0026others(3): Show | 6 | HG02257.hp2 HG02818.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.54-3145C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982690 | ||||||
chr5:112982716 | G | A | 10 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(7): Show | 11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-3119G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982716 | ||||||
chr5:112982848 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.54-2987A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982848 | ||||||
chr5:112983231 | C | T | 172 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(169): Show | 178 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.54-2604C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983231 | ||||||
chr5:112983344 | C | T | 84 | a0001c0001t0006g0022a0001c0001t0006g0114a0001c0001t0045g0067others(81): Show | 87 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.54-2491C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983344 | ||||||
chr5:112983399 | A | G | 12 | a0001c0001t0005g0127a0001c0001t0005g0219a0001c0001t0030g0123others(9): Show | 14 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.54-2436A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983399 | ||||||
chr5:112983415 | T | A | 171 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(168): Show | 177 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.54-2420T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983415 | ||||||
chr5:112983429 | C | T | 1 | a0001c0010t0070g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.54-2406C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983429 | ||||||
chr5:112983571 | A | G | 2 | a0001c0001t0007g0031a0001c0001t0007g0032 | 2 | NA19002.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.54-2264A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983571 | ||||||
chr5:112983660 | G | T | 1 | a0001c0002t0002g0108 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.54-2175G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983660 | ||||||
chr5:112983670 | G | A | 1 | a0001c0002t0008g0053 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.54-2165G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983670 | ||||||
chr5:112983699 | A | G | 4 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(1): Show | 4 | NA18945.hp1 NA19030.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-2136A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983699 | ||||||
chr5:112983794 | G | A | 10 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(7): Show | 11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-2041G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983794 | ||||||
chr5:112984103 | G | A | 3 | a0001c0001t0022g0215a0001c0001t0022g0216a0001c0001t0022g0217 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.54-1732G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984103 | ||||||
chr5:112984208 | A | G | 1 | a0001c0001t0006g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.54-1627A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984208 | ||||||
chr5:112984273 | G | C | 7 | a0001c0001t0005g0162a0001c0001t0011g0159a0001c0001t0011g0160others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.54-1562G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984273 | ||||||
chr5:112984420 | C | G | 4 | a0001c0001t0040g0333a0001c0001t0040g0334a0001c0001t0107g0126others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-1415C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984420 | ||||||
chr5:112984561 | C | T | 8 | a0001c0001t0015g0024a0001c0001t0015g0025a0001c0001t0015g0026others(5): Show | 8 | HG02257.hp2 HG02818.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-1274C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984561 | ||||||
chr5:112984641 | G | A | 1 | a0001c0002t0002g0054 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.54-1194G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984641 | ||||||
chr5:112984643 | C | G | 1 | a0001c0002t0002g0021 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.54-1192C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984643 | ||||||
chr5:112984652 | C | T | 10 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(7): Show | 11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-1183C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984652 | ||||||
chr5:112984663 | C | G | 2 | a0001c0001t0018g0330a0001c0001t0018g0331 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.54-1172C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984663 | ||||||
chr5:112984684 | A | AT | 12 | a0001c0001t0003g0169a0001c0001t0003g0180a0001c0001t0003g0184others(9): Show | 12 | HG01106.hp1 HG02015.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.54-1149dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984684 | |||||
chr5:112984686 | T | TTA | 4 | a0001c0001t0003g0144a0001c0001t0003g0185a0001c0001t0003g0190others(1): Show | 4 | HG01515.hp1 HG03471.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-1149_54-1148ins others(2): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984686 | ||||||
chr5:112984686 | T | TTAA | 13 | a0001c0001t0003g0145a0001c0001t0003g0146a0001c0001t0003g0174others(10): Show | 14 | HG03490.hp2 HG03491.hp2 HG03492.hp1 others(11): Show |
intron_variant | MODIFIER | c.54-1149_54-1148ins others(3): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984686 | ||||||
chr5:112984686 | TA | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0227a0001c0001t0001g0237others(8): Show | 13 | HG01261.hp2 HG02735.hp2 HG03041.hp2 others(10): Show |
intron_variant | MODIFIER | c.54-1131delA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984686 | |||||
chr5:112984687 | A | T | 156 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0003g0173others(153): Show | 160 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.54-1148A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984687 | ||||||
chr5:112984693 | A | ATATATAT others(4): Show |
2 | a0001c0001t0024g0201a0001c0001t0024g0202 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.54-1142_54-1141ins others(11): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984693 | ||||||
chr5:112984693 | A | ATATATAT others(24): Show |
1 | a0001c0002t0014g0107 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.54-1142_54-1141ins others(31): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984693 | ||||||
chr5:112984693 | A | T | 5 | a0001c0004t0019g0020a0001c0004t0019g0133a0001c0004t0019g0134others(2): Show | 5 | HG00741.hp1 HG01891.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.54-1142A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984693 | ||||||
chr5:112984694 | AAAAAAAA others(6): Show |
A | 1 | a0001c0002t0014g0106 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.54-1139_54-1127del others(13): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984694 | |||||
chr5:112984695 | A | AATATATA others(7): Show |
1 | a0001c0002t0064g0104 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.54-1139_54-1138ins others(14): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984695 | |||||
chr5:112984695 | A | ATATATAT others(16): Show |
1 | a0001c0002t0002g0105 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.54-1140_54-1139ins others(23): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984695 | ||||||
chr5:112984695 | A | T | 8 | a0001c0001t0024g0201a0001c0001t0024g0202a0001c0002t0014g0107others(5): Show | 8 | HG00741.hp1 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-1140A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984695 | ||||||
chr5:112984697 | A | AAT | 5 | a0001c0002t0048g0052a0001c0003t0005g0006a0001c0003t0005g0007others(2): Show | 7 | HG01884.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.54-1137_54-1136ins others(2): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984697 | |||||
chr5:112984697 | A | AATATATA others(3): Show |
1 | a0001c0002t0027g0050 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.54-1137_54-1136ins others(10): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984697 | |||||
chr5:112984697 | A | AATATATA others(11): Show |
1 | a0001c0001t0015g0027 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.54-1137_54-1136ins others(18): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984697 | |||||
chr5:112984697 | A | AATATATA others(13): Show |
2 | a0001c0001t0015g0026a0001c0001t0044g0143 | 2 | HG03195.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.54-1137_54-1136ins others(20): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984697 | |||||
chr5:112984697 | A | AATATATA others(17): Show |
2 | a0001c0001t0015g0025a0001c0002t0002g0100 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.54-1137_54-1136ins others(24): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984697 | |||||
chr5:112984697 | A | AATATATA others(21): Show |
3 | a0001c0001t0015g0024a0001c0002t0002g0098a0001c0002t0002g0099 | 3 | HG01167.hp1 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.54-1137_54-1136ins others(28): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984697 | |||||
chr5:112984697 | A | AATATATA others(23): Show |
2 | a0001c0002t0028g0125a0001c0002t0028g0135 | 2 | NA19074.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.54-1137_54-1136ins others(30): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984697 | |||||
chr5:112984697 | A | AATATATA others(27): Show |
1 | a0001c0002t0002g0046 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.54-1137_54-1136ins others(34): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984697 | |||||
chr5:112984697 | A | ATATATAT others(6): Show |
1 | a0001c0004t0046g0103 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.54-1138_54-1137ins others(13): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984697 | ||||||
chr5:112984697 | A | ATATATAT others(8): Show |
1 | a0001c0002t0008g0053 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.54-1138_54-1137ins others(15): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984697 | ||||||
chr5:112984697 | A | ATATATAT others(26): Show |
2 | a0001c0001t0030g0124a0001c0002t0063g0102 | 2 | NA18990.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.54-1138_54-1137ins others(33): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984697 | ||||||
chr5:112984697 | A | T | 11 | a0001c0001t0024g0201a0001c0001t0024g0202a0001c0002t0002g0105others(8): Show | 11 | HG00280.hp2 HG00741.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-1138A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984697 | ||||||
chr5:112984699 | A | AATATATA others(9): Show |
2 | a0001c0001t0011g0164a0001c0002t0059g0091 | 2 | HG02258.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.54-1135_54-1134ins others(16): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984699 | |||||
chr5:112984699 | A | AATATATA others(13): Show |
3 | a0001c0002t0002g0088a0001c0002t0002g0089a0001c0002t0053g0090 | 3 | NA18972.hp1 NA18977.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.54-1135_54-1134ins others(20): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984699 | |||||
chr5:112984699 | A | AATATATA others(15): Show |
1 | a0001c0002t0009g0087 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.54-1135_54-1134ins others(22): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984699 | |||||
chr5:112984699 | A | AATATATA others(17): Show |
1 | a0001c0001t0038g0023 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.54-1135_54-1134ins others(24): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984699 | |||||
chr5:112984699 | A | AATATATA others(19): Show |
1 | a0001c0002t0009g0086 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.54-1135_54-1134ins others(26): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984699 | |||||
chr5:112984699 | A | AATATATA others(21): Show |
2 | a0001c0001t0071g0028a0001c0002t0009g0085 | 2 | HG02135.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.54-1135_54-1134ins others(28): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984699 | |||||
chr5:112984699 | A | AATATATA others(31): Show |
1 | a0001c0002t0002g0084 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.54-1135_54-1134ins others(38): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984699 | |||||
chr5:112984699 | A | AATATATA others(35): Show |
1 | a0001c0002t0002g0083 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.54-1135_54-1134ins others(42): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984699 | |||||
chr5:112984699 | A | AT | 5 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0327others(2): Show | 5 | HG00140.hp1 HG01192.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.54-1136_54-1135ins others(1): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | ||||||
chr5:112984699 | A | ATAT | 1 | a0001c0002t0002g0001 | 3 | NA18955.hp2 NA18983.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.54-1136_54-1135ins others(3): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | ||||||
chr5:112984699 | A | ATATATAT others(4): Show |
2 | a0001c0001t0104g0158a0001c0001t0105g0151 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.54-1136_54-1135ins others(11): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | ||||||
chr5:112984699 | A | ATATATAT others(6): Show |
2 | a0001c0002t0008g0096a0001c0002t0061g0097 | 2 | NA18942.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.54-1136_54-1135ins others(13): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | ||||||
chr5:112984699 | A | ATATATAT others(8): Show |
1 | a0001c0002t0008g0095 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.54-1136_54-1135ins others(15): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | ||||||
chr5:112984699 | A | ATATATAT others(10): Show |
1 | a0001c0002t0002g0094 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.54-1136_54-1135ins others(17): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | ||||||
chr5:112984699 | A | ATATATAT others(14): Show |
2 | a0001c0001t0024g0166a0001c0002t0008g0130 | 2 | HG03516.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.54-1136_54-1135ins others(21): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | ||||||
chr5:112984699 | A | ATATATAT others(16): Show |
2 | a0001c0001t0011g0165a0001c0002t0002g0051 | 2 | HG02622.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.54-1136_54-1135ins others(23): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | ||||||
chr5:112984699 | A | ATATATAT others(20): Show |
2 | a0001c0002t0051g0093a0001c0002t0057g0092 | 2 | HG02074.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.54-1136_54-1135ins others(27): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | ||||||
chr5:112984699 | A | ATATATAT others(24): Show |
1 | a0001c0001t0030g0123 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.54-1136_54-1135ins others(31): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | ||||||
chr5:112984699 | A | T | 38 | a0001c0001t0001g0328a0001c0001t0005g0127a0001c0001t0015g0024others(35): Show | 40 | HG00280.hp2 HG00735.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.54-1136A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | ||||||
chr5:112984701 | A | AATATATA others(3): Show |
1 | a0001c0001t0107g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.54-1133_54-1132ins others(10): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984701 | |||||
chr5:112984701 | A | AATATATA others(17): Show |
1 | a0001c0002t0027g0072 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.54-1133_54-1132ins others(24): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984701 | |||||
chr5:112984701 | A | AATATATA others(19): Show |
1 | a0001c0002t0002g0108 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.54-1133_54-1132ins others(26): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984701 | |||||
chr5:112984701 | A | AATATATA others(21): Show |
1 | a0001c0002t0002g0071 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.54-1133_54-1132ins others(28): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984701 | |||||
chr5:112984701 | A | AATATATA others(23): Show |
1 | a0001c0001t0005g0162 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54-1133_54-1132ins others(30): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984701 | |||||
chr5:112984701 | A | AATATATA others(25): Show |
1 | a0001c0002t0002g0070 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.54-1133_54-1132ins others(32): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984701 | |||||
chr5:112984701 | A | AATATATA others(27): Show |
2 | a0001c0002t0009g0069a0001c0002t0014g0005 | 3 | HG00408.hp1 NA18989.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.54-1133_54-1132ins others(34): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984701 | |||||
chr5:112984701 | A | AATATATA others(51): Show |
1 | a0001c0001t0006g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.54-1133_54-1132ins others(58): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984701 | |||||
chr5:112984701 | A | AT | 14 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(11): Show | 15 | HG00423.hp1 HG01256.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.54-1134_54-1133ins others(1): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984701 | ||||||
chr5:112984701 | A | ATATATAT others(10): Show |
3 | a0001c0002t0008g0080a0001c0002t0008g0081a0001c0002t0008g0082 | 3 | HG00423.hp2 HG01943.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.54-1134_54-1133ins others(17): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984701 | ||||||
chr5:112984701 | A | ATATATAT others(14): Show |
1 | a0001c0001t0006g0200 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54-1134_54-1133ins others(21): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984701 | ||||||
chr5:112984701 | A | ATATATAT others(16): Show |
2 | a0001c0001t0011g0163a0001c0002t0056g0113 | 2 | HG02896.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.54-1134_54-1133ins others(23): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984701 | ||||||
chr5:112984701 | A | ATATATAT others(18): Show |
2 | a0001c0002t0008g0055a0001c0002t0058g0079 | 2 | HG00621.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.54-1134_54-1133ins others(25): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984701 | ||||||
chr5:112984701 | A | ATATATAT others(24): Show |
1 | a0001c0002t0002g0078 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.54-1134_54-1133ins others(31): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984701 | ||||||
chr5:112984701 | A | ATATATAT others(26): Show |
1 | a0001c0002t0009g0077 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.54-1134_54-1133ins others(33): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984701 | ||||||
chr5:112984701 | A | ATATATAT others(28): Show |
2 | a0001c0002t0002g0075a0001c0002t0002g0076 | 2 | HG01975.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.54-1134_54-1133ins others(35): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984701 | ||||||
chr5:112984701 | A | T | 95 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0314others(92): Show | 103 | HG00140.hp1 HG00280.hp2 HG00673.hp1 others(100): Show |
intron_variant | MODIFIER | c.54-1134A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984701 | ||||||
chr5:112984703 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0065g0044 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(18): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0007g0031 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(20): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAAAAAT others(6): Show |
1 | a0001c0001t0111g0152 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(13): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAAAAAT others(8): Show |
1 | a0001c0001t0007g0033 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(15): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAAAAAT others(16): Show |
1 | a0001c0001t0069g0040 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(23): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAAAATA others(9): Show |
2 | a0001c0001t0007g0035a0001c0001t0013g0155 | 2 | HG03209.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(16): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAAAATA others(11): Show |
3 | a0001c0001t0007g0034a0001c0001t0007g0045a0001c0001t0013g0154 | 3 | HG02886.hp2 NA19057.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(18): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAAAATA others(13): Show |
2 | a0001c0001t0007g0032a0001c0001t0007g0041 | 2 | NA19065.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(20): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAAAATA others(19): Show |
1 | a0001c0001t0013g0153 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(26): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAAATAT others(6): Show |
2 | a0001c0001t0013g0147a0001c0001t0113g0156 | 2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(13): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAAATAT others(14): Show |
1 | a0001c0001t0067g0042 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(21): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAAATAT others(22): Show |
2 | a0001c0002t0002g0054a0001c0002t0002g0218 | 2 | HG01081.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(29): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAAATAT others(32): Show |
1 | a0001c0002t0025g0056 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(39): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAAATAT others(34): Show |
1 | a0001c0010t0070g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(41): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAATATA others(3): Show |
1 | a0001c0002t0049g0110 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(10): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAATATA others(9): Show |
1 | a0001c0001t0007g0039 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(16): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAATATA others(11): Show |
2 | a0001c0001t0007g0038a0001c0001t0068g0037 | 2 | HG02129.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(18): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAATATA others(13): Show |
1 | a0001c0002t0002g0057 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(20): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAATATA others(15): Show |
2 | a0001c0001t0066g0036a0001c0002t0002g0136 | 2 | HG02040.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(22): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAATATA others(17): Show |
3 | a0001c0001t0006g0138a0001c0001t0042g0139a0001c0002t0002g0109 | 3 | HG01981.hp2 HG02155.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(24): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAATATA others(19): Show |
2 | a0001c0001t0006g0196a0001c0002t0002g0111 | 2 | HG02683.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(26): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAAATATA others(29): Show |
1 | a0001c0002t0002g0115 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(36): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAATAT | 6 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0003g0173others(3): Show | 6 | HG04115.hp2 NA18945.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(5): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAATATAT others(8): Show |
1 | a0001c0001t0029g0029 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(15): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAATATAT others(10): Show |
1 | a0001c0001t0007g0018 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(17): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAATATAT others(12): Show |
1 | a0001c0002t0002g0060 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(19): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAATATAT others(16): Show |
1 | a0001c0001t0006g0140 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(23): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAATATAT others(22): Show |
1 | a0001c0002t0054g0049 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(29): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAATATAT others(24): Show |
1 | a0001c0002t0025g0129 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(31): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAATATAT others(26): Show |
2 | a0001c0002t0002g0058a0001c0002t0002g0059 | 2 | HG01346.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(33): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAATATAT others(36): Show |
1 | a0001c0002t0052g0048 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(43): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AAATATAT others(38): Show |
1 | a0001c0002t0002g0210 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(45): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AATATATA others(7): Show |
1 | a0001c0001t0029g0030 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.54-1123_54-1110dup others(14): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AATATATA others(17): Show |
4 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0043g0195others(1): Show | 4 | HG01243.hp1 NA18747.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-1110_54-1109ins others(24): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AATATATA others(19): Show |
1 | a0001c0001t0011g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.54-1110_54-1109ins others(26): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AATATATA others(23): Show |
2 | a0001c0002t0050g0064a0001c0007t0055g0047 | 2 | HG02922.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.54-1110_54-1109ins others(30): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AATATATA others(25): Show |
1 | a0001c0002t0002g0063 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.54-1110_54-1109ins others(32): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AATATATA others(27): Show |
1 | a0001c0002t0002g0116 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.54-1110_54-1109ins others(34): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AATATATA others(29): Show |
1 | a0001c0002t0002g0062 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.54-1110_54-1109ins others(36): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | AATATATA others(35): Show |
1 | a0001c0002t0002g0061 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.54-1110_54-1109ins others(42): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | |||||
chr5:112984703 | A | ATATATAT others(4): Show |
1 | a0001c0002t0002g0112 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.54-1132_54-1131ins others(11): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | ||||||
chr5:112984703 | A | ATATATAT others(8): Show |
1 | a0001c0001t0013g0157 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.54-1132_54-1131ins others(15): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | ||||||
chr5:112984703 | A | ATATATAT others(10): Show |
2 | a0001c0001t0006g0141a0001c0002t0008g0068 | 2 | NA18968.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.54-1132_54-1131ins others(17): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | ||||||
chr5:112984703 | A | ATATATAT others(16): Show |
2 | a0001c0001t0006g0114a0001c0001t0038g0161 | 2 | HG02630.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.54-1132_54-1131ins others(23): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | ||||||
chr5:112984703 | A | ATATATAT others(18): Show |
1 | a0001c0001t0045g0067 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.54-1132_54-1131ins others(25): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | ||||||
chr5:112984703 | A | ATATATAT others(20): Show |
2 | a0001c0001t0006g0199a0001c0001t0011g0160 | 2 | HG03516.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.54-1132_54-1131ins others(27): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | ||||||
chr5:112984703 | A | ATATATAT others(22): Show |
1 | a0001c0001t0006g0137 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.54-1132_54-1131ins others(29): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | ||||||
chr5:112984703 | A | ATATATAT others(24): Show |
2 | a0001c0002t0002g0021a0001c0002t0002g0066 | 2 | HG01243.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.54-1132_54-1131ins others(31): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | ||||||
chr5:112984703 | A | ATATATAT others(32): Show |
1 | a0001c0002t0002g0065 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.54-1132_54-1131ins others(39): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | ||||||
chr5:112984703 | A | T | 238 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(235): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.54-1132A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | ||||||
chr5:112984720 | A | ATG | 10 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(7): Show | 11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-1114_54-1113ins others(2): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984720 | |||||
chr5:112984722 | A | ATATATAT others(31): Show |
1 | a0001c0001t0012g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.54-1110_54-1109ins others(38): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984722 | |||||
chr5:112984722 | A | ATATATAT others(25): Show |
1 | a0001c0002t0103g0149 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.54-1110_54-1109ins others(32): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984722 | |||||
chr5:112984740 | C | T | 2 | a0001c0001t0001g0337a0001c0002t0103g0149 | 2 | HG03486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.54-1095C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984740 | ||||||
chr5:112984829 | C | T | 1 | a0001c0001t0082g0292 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.54-1006C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984829 | ||||||
chr5:112984838 | AG | A | 184 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(181): Show | 189 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.54-995delG | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984838 | |||||
chr5:112984860 | A | G | 10 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(7): Show | 11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-975A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984860 | ||||||
chr5:112984981 | G | A | 212 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(209): Show | 220 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.54-854G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984981 | ||||||
chr5:112985057 | C | G | 18 | a0001c0001t0007g0018a0001c0001t0007g0031a0001c0001t0007g0032others(15): Show | 18 | HG00609.hp1 HG02129.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.54-778C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985057 | ||||||
chr5:112985062 | G | A | 4 | a0001c0002t0002g0075a0001c0002t0002g0098a0001c0002t0002g0100others(1): Show | 4 | HG02559.hp1 HG02615.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-773G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985062 | ||||||
chr5:112985225 | G | A | 10 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(7): Show | 11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-610G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985225 | ||||||
chr5:112985228 | A | G | 1 | a0001c0001t0111g0152 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.54-607A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985228 | ||||||
chr5:112985252 | G | A | 54 | a0001c0001t0006g0022a0001c0001t0006g0114a0001c0001t0045g0067others(51): Show | 57 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.54-583G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985252 | ||||||
chr5:112985256 | A | T | 1 | a0001c0001t0003g0184 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.54-579A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985256 | ||||||
chr5:112985270 | G | T | 96 | a0001c0001t0006g0022a0001c0001t0006g0114a0001c0001t0006g0137others(93): Show | 99 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.54-565G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985270 | ||||||
chr5:112985334 | G | A | 194 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(191): Show | 200 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.54-501G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985334 | ||||||
chr5:112985373 | T | C | 194 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(191): Show | 200 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.54-462T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985373 | ||||||
chr5:112985426 | A | G | 7 | a0001c0001t0005g0162a0001c0001t0011g0159a0001c0001t0011g0160others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.54-409A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985426 | ||||||
chr5:112985478 | A | G | 1 | a0001c0003t0005g0120 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.54-357A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985478 | ||||||
chr5:112985522 | A | G | 1 | a0001c0002t0002g0105 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.54-313A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985522 | ||||||
chr5:112985603 | A | G | 3 | a0001c0001t0024g0166a0001c0001t0024g0201a0001c0001t0024g0202 | 3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.54-232A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985603 | ||||||
chr5:112985681 | T | C | 1 | a0001c0001t0084g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.54-154T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985681 | ||||||
chr5:112985751 | G | T | 7 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(4): Show | 8 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-84G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985751 | ||||||
chr5:112985769 | A | T | 2 | a0001c0001t0029g0029a0001c0001t0029g0030 | 2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.54-66A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985769 | ||||||
chr5:112985774 | G | T | 10 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(7): Show | 11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-61G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985774 | ||||||
chr5:112985791 | A | G | 97 | a0001c0001t0006g0022a0001c0001t0006g0114a0001c0001t0006g0137others(94): Show | 100 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.54-44A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985791 | ||||||
chr5:112985827 | T | C | 1 | a0001c0001t0001g0239 | 1 | NA18612.hp2 | splice_region_variant&intron_variant | LOW | c.54-8T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985827 | ||||||
chr5:112986046 | T | A | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | NA18999.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.205+60T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986046 | ||||||
chr5:112986060 | C | T | 10 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(7): Show | 11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.205+74C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986060 | ||||||
chr5:112986069 | A | G | 7 | a0001c0003t0005g0006a0001c0003t0005g0007a0001c0003t0005g0118others(4): Show | 9 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.205+83A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986069 | ||||||
chr5:112986246 | T | C | 1 | a0001c0001t0112g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.205+260T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986246 | ||||||
chr5:112986341 | CT | C | 88 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(85): Show | 90 | HG00609.hp1 HG01074.hp2 HG01106.hp1 others(87): Show |
intron_variant | MODIFIER | c.205+367delT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112986341 | |||||
chr5:112986342 | T | C | 14 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0140others(11): Show | 14 | HG02155.hp2 HG02602.hp2 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.205+356T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986342 | ||||||
chr5:112986398 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.205+412T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986398 | ||||||
chr5:112986499 | A | G | 10 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(7): Show | 11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.205+513A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986499 | ||||||
chr5:112986585 | A | G | 10 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(7): Show | 11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.205+599A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986585 | ||||||
chr5:112986623 | C | A | 1 | a0001c0009t0021g0240 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.205+637C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986623 | ||||||
chr5:112986624 | C | T | 1 | a0001c0001t0047g0117 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.205+638C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986624 | ||||||
chr5:112986628 | G | A | 1 | a0001c0002t0002g0218 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.205+642G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986628 | ||||||
chr5:112986753 | C | A | 1 | a0001c0001t0112g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.205+767C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986753 | ||||||
chr5:112986842 | G | C | 1 | a0001c0002t0002g0001 | 3 | NA18955.hp2 NA18983.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.205+856G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986842 | ||||||
chr5:112986880 | A | G | 107 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(104): Show | 111 | HG00609.hp1 HG01074.hp2 HG01106.hp1 others(108): Show |
intron_variant | MODIFIER | c.205+894A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986880 | ||||||
chr5:112986935 | G | A | 2 | a0001c0001t0016g0241a0001c0001t0016g0313 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.205+949G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986935 | ||||||
chr5:112987158 | C | T | 1 | a0001c0001t0006g0141 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.205+1172C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987158 | ||||||
chr5:112987379 | G | T | 1 | a0001c0001t0003g0146 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.205+1393G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987379 | ||||||
chr5:112987440 | T | G | 3 | a0001c0001t0022g0215a0001c0001t0022g0216a0001c0001t0022g0217 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.205+1454T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987440 | ||||||
chr5:112987608 | A | G | 107 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(104): Show | 110 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.205+1622A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987608 | ||||||
chr5:112987620 | C | CT | 80 | a0001c0001t0001g0014a0001c0001t0001g0227a0001c0001t0001g0235others(77): Show | 83 | HG00673.hp1 HG01074.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.205+1659dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112987620 | |||||
chr5:112987620 | C | CTT | 29 | a0001c0001t0001g0285a0001c0001t0003g0169a0001c0001t0003g0173others(26): Show | 30 | HG01106.hp1 HG01433.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.205+1658_205+1659d others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112987620 | |||||
chr5:112987620 | C | CTTT | 19 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(16): Show | 19 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.205+1657_205+1659d others(5): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112987620 | |||||
chr5:112987620 | C | CTTTTT | 26 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0141others(23): Show | 26 | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.205+1655_205+1659d others(7): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112987620 | |||||
chr5:112987620 | C | CTTTTTT | 49 | a0001c0001t0005g0162a0001c0001t0006g0022a0001c0001t0006g0140others(46): Show | 52 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.205+1654_205+1659d others(8): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112987620 | |||||
chr5:112987620 | C | CTTTTTTT | 22 | a0001c0001t0006g0198a0001c0001t0045g0067a0001c0001t0112g0128others(19): Show | 22 | HG00280.hp2 HG00423.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.205+1653_205+1659d others(9): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112987620 | |||||
chr5:112987620 | C | CTTTTTTT others(3): Show |
1 | a0001c0002t0025g0129 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.205+1650_205+1659d others(12): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112987620 | |||||
chr5:112987620 | CTTT | C | 10 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(7): Show | 11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.205+1657_205+1659d others(5): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112987620 | |||||
chr5:112987624 | T | C | 10 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(7): Show | 11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.205+1638T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987624 | ||||||
chr5:112987628 | T | G | 1 | a0001c0001t0094g0224 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.205+1642T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987628 | ||||||
chr5:112987661 | A | G | 1 | a0001c0001t0006g0141 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.205+1675A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987661 | ||||||
chr5:112987705 | G | C | 214 | a0001c0001t0001g0269a0001c0001t0001g0286a0001c0001t0001g0287others(211): Show | 222 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.205+1719G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987705 | ||||||
chr5:112987744 | G | A | 1 | a0001c0002t0002g0111 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.205+1758G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987744 | ||||||
chr5:112987745 | A | T | 6 | a0001c0002t0002g0057a0001c0002t0002g0060a0001c0002t0002g0136others(3): Show | 6 | HG00639.hp2 HG01358.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.205+1759A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987745 | ||||||
chr5:112987747 | T | A | 1 | a0001c0001t0093g0242 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.205+1761T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987747 | ||||||
chr5:112987793 | C | CT | 10 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(7): Show | 11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.205+1817dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112987793 | |||||
chr5:112987830 | C | T | 2 | a0001c0001t0006g0140a0001c0001t0042g0139 | 2 | NA18948.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.205+1844C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987830 | ||||||
chr5:112987877 | C | T | 24 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0003g0173others(21): Show | 25 | HG02602.hp1 HG03490.hp2 HG03491.hp2 others(22): Show |
intron_variant | MODIFIER | c.205+1891C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987877 | ||||||
chr5:112987878 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.205+1892G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987878 | ||||||
chr5:112987909 | G | A | 1 | a0001c0001t0044g0143 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.205+1923G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987909 | ||||||
chr5:112987914 | C | T | 117 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(114): Show | 125 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.205+1928C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987914 | ||||||
chr5:112987915 | G | C | 1 | a0001c0002t0049g0110 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.205+1929G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987915 | ||||||
chr5:112988041 | A | G | 214 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0326others(211): Show | 222 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.205+2055A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988041 | ||||||
chr5:112988089 | T | C | 1 | a0001c0010t0070g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.205+2103T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988089 | ||||||
chr5:112988159 | C | T | 4 | a0001c0001t0003g0169a0001c0001t0003g0189a0001c0001t0075g0188others(1): Show | 4 | HG00280.hp2 HG01106.hp1 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.205+2173C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988159 | ||||||
chr5:112988195 | A | G | 1 | a0001c0002t0050g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.205+2209A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988195 | ||||||
chr5:112988220 | T | C | 63 | a0001c0001t0001g0235a0001c0001t0001g0306a0001c0001t0001g0314others(60): Show | 66 | HG01243.hp1 HG01496.hp1 HG01496.hp2 others(63): Show |
intron_variant | MODIFIER | c.205+2234T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988220 | ||||||
chr5:112988232 | C | G | 1 | a0001c0001t0001g0310 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.205+2246C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988232 | ||||||
chr5:112988318 | T | TA | 164 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(161): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.205+2347dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112988318 | |||||
chr5:112988318 | T | TAA | 8 | a0001c0001t0001g0243a0001c0001t0003g0145a0001c0001t0003g0180others(5): Show | 8 | HG01074.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.205+2346_205+2347d others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112988318 | |||||
chr5:112988319 | A | G | 1 | a0001c0001t0013g0153 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.205+2333A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988319 | ||||||
chr5:112988348 | T | C | 1 | a0001c0002t0002g0054 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.205+2362T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988348 | ||||||
chr5:112988363 | G | A | 47 | a0001c0001t0001g0295a0001c0001t0003g0144a0001c0001t0003g0146others(44): Show | 47 | HG00741.hp1 HG01891.hp1 HG02015.hp1 others(44): Show |
intron_variant | MODIFIER | c.205+2377G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988363 | ||||||
chr5:112988441 | G | A | 1 | a0001c0002t0002g0218 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.205+2455G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988441 | ||||||
chr5:112988449 | G | C | 2 | a0001c0001t0040g0333a0001c0001t0040g0334 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.205+2463G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988449 | ||||||
chr5:112988494 | T | TA | 40 | a0001c0001t0001g0243a0001c0001t0001g0261a0001c0001t0001g0262others(37): Show | 41 | HG00140.hp2 HG00609.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.205+2532dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112988494 | |||||
chr5:112988494 | T | TAA | 145 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(142): Show | 153 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.205+2531_205+2532d others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112988494 | |||||
chr5:112988494 | T | TAAA | 38 | a0001c0001t0001g0012a0001c0001t0001g0247a0001c0001t0001g0272others(35): Show | 39 | HG00621.hp2 HG00735.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.205+2530_205+2532d others(5): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112988494 | |||||
chr5:112988494 | T | TAAAAA | 7 | a0001c0001t0001g0235a0001c0001t0017g0010a0001c0001t0017g0214others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.205+2528_205+2532d others(7): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112988494 | |||||
chr5:112988494 | TA | T | 28 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0140others(25): Show | 28 | HG00423.hp2 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.205+2532delA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112988494 | |||||
chr5:112988520 | G | A | 1 | a0001c0001t0004g0323 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.205+2534G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988520 | ||||||
chr5:112988546 | G | A | 1 | a0001c0002t0002g0084 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.205+2560G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988546 | ||||||
chr5:112988650 | C | A | 1 | a0001c0001t0036g0248 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.205+2664C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988650 | ||||||
chr5:112988655 | T | C | 1 | a0001c0001t0001g0303 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.205+2669T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988655 | ||||||
chr5:112988703 | T | C | 5 | a0001c0004t0019g0020a0001c0004t0019g0133a0001c0004t0019g0134others(2): Show | 5 | HG00741.hp1 HG01891.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.205+2717T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988703 | ||||||
chr5:112988799 | G | A | 344 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(341): Show | 360 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.205+2813G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988799 | ||||||
chr5:112989047 | T | C | 17 | a0001c0001t0015g0024a0001c0001t0015g0025a0001c0001t0015g0026others(14): Show | 19 | HG01496.hp1 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.205+3061T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989047 | ||||||
chr5:112989073 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.206-3048A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989073 | ||||||
chr5:112989081 | G | C | 1 | a0001c0001t0001g0303 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.206-3040G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989081 | ||||||
chr5:112989090 | C | T | 1 | a0001c0001t0112g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.206-3031C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989090 | ||||||
chr5:112989092 | G | A | 80 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(77): Show | 84 | HG01074.hp2 HG01106.hp1 HG01496.hp1 others(81): Show |
intron_variant | MODIFIER | c.206-3029G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989092 | ||||||
chr5:112989120 | G | C | 1 | a0001c0001t0074g0170 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.206-3001G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989120 | ||||||
chr5:112989205 | C | A | 1 | a0001c0001t0001g0249 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.206-2916C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989205 | ||||||
chr5:112989428 | C | CA | 7 | a0001c0001t0003g0191a0001c0001t0006g0022a0001c0001t0010g0304others(4): Show | 7 | HG02280.hp2 HG03098.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.206-2680dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112989428 | |||||
chr5:112989476 | A | T | 7 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(4): Show | 8 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.206-2645A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989476 | ||||||
chr5:112989541 | A | G | 2 | a0001c0001t0021g0299a0001c0001t0021g0300 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.206-2580A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989541 | ||||||
chr5:112989597 | A | G | 1 | a0001c0001t0112g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.206-2524A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989597 | ||||||
chr5:112989650 | T | G | 1 | a0001c0001t0030g0124 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.206-2471T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989650 | ||||||
chr5:112989653 | G | T | 1 | a0001c0001t0112g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.206-2468G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989653 | ||||||
chr5:112989854 | A | G | 1 | a0001c0002t0008g0055 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.206-2267A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989854 | ||||||
chr5:112989899 | T | C | 1 | a0001c0001t0112g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.206-2222T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989899 | ||||||
chr5:112989919 | A | T | 1 | a0001c0001t0005g0162 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.206-2202A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989919 | ||||||
chr5:112989926 | GTGA | G | 93 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(90): Show | 97 | HG01074.hp2 HG01106.hp1 HG01496.hp1 others(94): Show |
intron_variant | MODIFIER | c.206-2190_206-2188d others(5): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112989926 | |||||
chr5:112990172 | C | T | 140 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(137): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.206-1949C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112990172 | ||||||
chr5:112990333 | T | C | 1 | a0001c0001t0004g0323 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.206-1788T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112990333 | ||||||
chr5:112990552 | T | C | 1 | a0001c0001t0066g0036 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.206-1569T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112990552 | ||||||
chr5:112990571 | C | T | 5 | a0001c0001t0001g0247a0001c0001t0001g0296a0001c0001t0004g0232others(2): Show | 5 | NA18960.hp1 NA18963.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.206-1550C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112990571 | ||||||
chr5:112990713 | G | A | 144 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(141): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.206-1408G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112990713 | ||||||
chr5:112990729 | A | T | 1 | a0001c0001t0007g0045 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.206-1392A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112990729 | ||||||
chr5:112990802 | GTAC | G | 93 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(90): Show | 97 | HG01074.hp2 HG01106.hp1 HG01496.hp1 others(94): Show |
intron_variant | MODIFIER | c.206-1315_206-1313d others(5): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112990802 | |||||
chr5:112990883 | AT | A | 143 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(140): Show | 152 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.206-1227delT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112990883 | |||||
chr5:112990953 | T | G | 17 | a0001c0001t0015g0024a0001c0001t0015g0025a0001c0001t0015g0026others(14): Show | 19 | HG01496.hp1 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.206-1168T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112990953 | ||||||
chr5:112991050 | A | G | 3 | a0001c0001t0012g0008a0001c0001t0012g0167a0001c0001t0012g0168 | 4 | HG01074.hp2 HG01891.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.206-1071A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112991050 | ||||||
chr5:112991254 | C | G | 57 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(54): Show | 58 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(55): Show |
intron_variant | MODIFIER | c.206-867C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112991254 | ||||||
chr5:112991258 | A | G | 2 | a0001c0001t0005g0127a0001c0001t0005g0219 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.206-863A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112991258 | ||||||
chr5:112991433 | C | T | 2 | a0001c0001t0001g0269a0001c0001t0004g0268 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.206-688C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112991433 | ||||||
chr5:112991561 | A | G | 1 | a0001c0001t0107g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.206-560A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112991561 | ||||||
chr5:112991633 | T | C | 1 | a0001c0002t0002g0076 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.206-488T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112991633 | ||||||
chr5:112991654 | T | G | 1 | a0001c0001t0112g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.206-467T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112991654 | ||||||
chr5:112991762 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.206-359C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112991762 | ||||||
chr5:112991936 | G | A | 1 | a0001c0001t0001g0310 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.206-185G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112991936 | ||||||
chr5:112992056 | C | T | 3 | a0001c0001t0012g0008a0001c0001t0012g0167a0001c0001t0012g0168 | 4 | HG01074.hp2 HG01891.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.206-65C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112992056 | ||||||
chr5:112992289 | C | T | 1 | a0001c0001t0107g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.333+41C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 3/10 | chr5 | 112992289 | ||||||
chr5:112992394 | T | C | 2 | a0001c0001t0104g0158a0001c0001t0105g0151 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.333+146T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 3/10 | chr5 | 112992394 | ||||||
chr5:112992396 | C | T | 1 | a0001c0001t0091g0222 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.333+148C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 3/10 | chr5 | 112992396 | ||||||
chr5:112992550 | A | G | 1 | a0001c0002t0008g0082 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.334-122A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 3/10 | chr5 | 112992550 | ||||||
chr5:112992570 | C | T | 110 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(107): Show | 114 | HG00609.hp1 HG01074.hp2 HG01106.hp1 others(111): Show |
intron_variant | MODIFIER | c.334-102C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 3/10 | chr5 | 112992570 | ||||||
chr5:112992900 | AC | A | 146 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(143): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.432+131delC | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112992900 | ||||||
chr5:112992901 | C | T | 1 | a0001c0001t0010g0304 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+131C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112992901 | ||||||
chr5:112992933 | T | G | 1 | a0001c0001t0015g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.432+163T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112992933 | ||||||
chr5:112993156 | T | A | 3 | a0001c0001t0022g0215a0001c0001t0022g0216a0001c0001t0022g0217 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.432+386T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993156 | ||||||
chr5:112993339 | A | G | 1 | a0001c0002t0050g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.432+569A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993339 | ||||||
chr5:112993366 | G | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(139): Show | 151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.432+596G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993366 | ||||||
chr5:112993440 | C | A | 6 | a0001c0001t0001g0238a0001c0004t0019g0020a0001c0004t0019g0133others(3): Show | 6 | HG00741.hp1 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.432+670C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993440 | ||||||
chr5:112993595 | G | C | 1 | a0001c0001t0007g0034 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.432+825G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993595 | ||||||
chr5:112993616 | C | G | 1 | a0001c0002t0103g0149 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.432+846C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993616 | ||||||
chr5:112993624 | C | CA | 14 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(11): Show | 14 | HG01891.hp2 HG01943.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.432+869dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112993624 | |||||
chr5:112993639 | A | C | 3 | a0001c0001t0024g0166a0001c0001t0024g0201a0001c0001t0024g0202 | 3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.432+869A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993639 | ||||||
chr5:112993640 | C | A | 8 | a0001c0001t0001g0247a0001c0001t0001g0251a0001c0001t0001g0286others(5): Show | 8 | HG01261.hp2 HG01981.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.432+870C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993640 | ||||||
chr5:112993642 | A | C | 7 | a0001c0001t0001g0247a0001c0001t0001g0251a0001c0001t0001g0286others(4): Show | 7 | HG01261.hp2 HG01981.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.432+872A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993642 | ||||||
chr5:112993653 | AC | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(132): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.432+885delC | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112993653 | |||||
chr5:112993654 | C | A | 7 | a0001c0001t0001g0247a0001c0001t0001g0251a0001c0001t0001g0286others(4): Show | 7 | HG01261.hp2 HG01981.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.432+884C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993654 | ||||||
chr5:112993881 | A | C | 257 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(254): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.432+1111A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993881 | ||||||
chr5:112993943 | A | G | 19 | a0001c0001t0007g0018a0001c0001t0007g0031a0001c0001t0007g0032others(16): Show | 19 | HG00609.hp1 HG01099.hp1 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.432+1173A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993943 | ||||||
chr5:112993970 | A | T | 1 | a0001c0002t0064g0104 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.432+1200A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993970 | ||||||
chr5:112994086 | C | T | 1 | a0001c0001t0001g0288 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.432+1316C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112994086 | ||||||
chr5:112994163 | C | CT | 41 | a0001c0001t0001g0014a0001c0001t0001g0247a0001c0001t0001g0251others(38): Show | 41 | HG00621.hp2 HG00741.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.432+1418dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112994163 | |||||
chr5:112994163 | CT | C | 22 | a0001c0001t0001g0238a0001c0001t0001g0252a0001c0001t0001g0284others(19): Show | 22 | HG01071.hp2 HG01256.hp1 HG02155.hp1 others(19): Show |
intron_variant | MODIFIER | c.432+1418delT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112994163 | |||||
chr5:112994221 | G | GA | 7 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(4): Show | 8 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.432+1452dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112994221 | |||||
chr5:112994260 | C | T | 17 | a0001c0001t0015g0024a0001c0001t0015g0025a0001c0001t0015g0026others(14): Show | 19 | HG01496.hp1 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.432+1490C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112994260 | ||||||
chr5:112994276 | A | G | 2 | a0001c0001t0001g0315a0001c0006t0035g0317 | 2 | NA19006.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.432+1506A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112994276 | ||||||
chr5:112994380 | C | T | 1 | a0001c0002t0002g0076 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.432+1610C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112994380 | ||||||
chr5:112994398 | CTAGGCTT others(7): Show |
C | 1 | a0001c0002t0061g0097 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.432+1629_432+1642d others(16): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112994398 | ||||||
chr5:112994451 | C | T | 2 | a0001c0002t0002g0078a0001c0002t0051g0093 | 2 | HG00609.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.432+1681C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112994451 | ||||||
chr5:112994452 | G | C | 1 | a0001c0010t0070g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.432+1682G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112994452 | ||||||
chr5:112994660 | T | C | 2 | a0001c0001t0001g0269a0001c0001t0004g0268 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.432+1890T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112994660 | ||||||
chr5:112994900 | T | G | 7 | a0001c0001t0013g0147a0001c0001t0013g0153a0001c0001t0013g0154others(4): Show | 7 | HG01496.hp2 HG02055.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.432+2130T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112994900 | ||||||
chr5:112995041 | A | C | 141 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(138): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.432+2271A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995041 | ||||||
chr5:112995058 | G | A | 1 | a0001c0001t0003g0185 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.432+2288G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995058 | ||||||
chr5:112995058 | G | C | 1 | a0001c0001t0004g0244 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.432+2288G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995058 | ||||||
chr5:112995111 | C | CAAAAAAT others(6): Show |
1 | a0001c0002t0061g0097 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.432+2345_432+2357d others(15): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112995111 | |||||
chr5:112995190 | A | G | 1 | a0001c0001t0024g0166 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.432+2420A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995190 | ||||||
chr5:112995232 | T | G | 3 | a0001c0001t0024g0166a0001c0001t0024g0201a0001c0001t0024g0202 | 3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.432+2462T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995232 | ||||||
chr5:112995282 | C | T | 17 | a0001c0001t0015g0024a0001c0001t0015g0025a0001c0001t0015g0026others(14): Show | 19 | HG01496.hp1 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.432+2512C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995282 | ||||||
chr5:112995344 | C | T | 1 | a0001c0001t0111g0152 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.432+2574C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995344 | ||||||
chr5:112995394 | G | C | 256 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(253): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.432+2624G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995394 | ||||||
chr5:112995465 | A | T | 1 | a0001c0001t0112g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.432+2695A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995465 | ||||||
chr5:112995582 | G | A | 1 | a0001c0001t0024g0166 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.432+2812G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995582 | ||||||
chr5:112995680 | C | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0263a0001c0001t0001g0298others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.432+2910C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995680 | ||||||
chr5:112995685 | T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0263a0001c0001t0001g0298others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.432+2915T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995685 | ||||||
chr5:112995782 | A | G | 1 | a0001c0010t0070g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.432+3012A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995782 | ||||||
chr5:112995973 | T | C | 1 | a0001c0008t0108g0236 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.432+3203T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995973 | ||||||
chr5:112996057 | C | G | 5 | a0001c0004t0019g0020a0001c0004t0019g0133a0001c0004t0019g0134others(2): Show | 5 | HG00741.hp1 HG01891.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+3287C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996057 | ||||||
chr5:112996105 | C | A | 1 | a0001c0003t0005g0119 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.432+3335C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996105 | ||||||
chr5:112996109 | T | C | 6 | a0001c0001t0004g0271a0001c0001t0004g0281a0001c0001t0099g0246others(3): Show | 6 | NA18966.hp2 NA18985.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.432+3339T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996109 | ||||||
chr5:112996161 | G | C | 10 | a0001c0001t0015g0024a0001c0001t0015g0025a0001c0001t0015g0026others(7): Show | 10 | HG01496.hp1 HG02257.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.432+3391G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996161 | ||||||
chr5:112996256 | A | G | 1 | a0001c0001t0004g0244 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.432+3486A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996256 | ||||||
chr5:112996328 | C | T | 1 | a0001c0001t0045g0067 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.432+3558C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996328 | ||||||
chr5:112996410 | T | A | 4 | a0001c0001t0001g0249a0001c0001t0001g0270a0001c0001t0087g0013others(1): Show | 4 | NA18943.hp1 NA18966.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+3640T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996410 | ||||||
chr5:112996519 | T | C | 1 | a0001c0001t0001g0276 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.432+3749T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996519 | ||||||
chr5:112996626 | A | G | 4 | a0001c0001t0012g0008a0001c0001t0012g0148a0001c0001t0012g0167others(1): Show | 5 | HG01074.hp2 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+3856A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996626 | ||||||
chr5:112996750 | C | A | 1 | a0001c0001t0001g0309 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.432+3980C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996750 | ||||||
chr5:112996960 | G | C | 1 | a0001c0001t0001g0272 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.433-4124G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996960 | ||||||
chr5:112997009 | C | T | 3 | a0001c0001t0024g0166a0001c0001t0024g0201a0001c0001t0024g0202 | 3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.433-4075C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997009 | ||||||
chr5:112997029 | T | C | 1 | a0001c0001t0023g0213 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.433-4055T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997029 | ||||||
chr5:112997030 | C | T | 1 | a0001c0001t0023g0213 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.433-4054C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997030 | ||||||
chr5:112997098 | A | G | 1 | a0001c0010t0070g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.433-3986A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997098 | ||||||
chr5:112997191 | G | A | 1 | a0001c0001t0001g0295 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.433-3893G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997191 | ||||||
chr5:112997202 | T | C | 3 | a0001c0001t0007g0041a0001c0001t0067g0042a0001c0001t0069g0040 | 3 | HG03209.hp2 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.433-3882T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997202 | ||||||
chr5:112997317 | G | T | 6 | a0001c0001t0005g0162a0001c0001t0011g0159a0001c0001t0011g0160others(3): Show | 6 | HG02258.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-3767G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997317 | ||||||
chr5:112997359 | G | A | 1 | a0001c0001t0034g0183 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.433-3725G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997359 | ||||||
chr5:112997486 | T | C | 10 | a0001c0001t0003g0169a0001c0001t0003g0180a0001c0001t0003g0185others(7): Show | 10 | HG01106.hp1 HG01515.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-3598T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997486 | ||||||
chr5:112997623 | T | C | 1 | a0001c0001t0012g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.433-3461T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997623 | ||||||
chr5:112997637 | T | A | 1 | a0001c0001t0001g0273 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.433-3447T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997637 | ||||||
chr5:112997826 | G | A | 1 | a0001c0008t0108g0236 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.433-3258G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997826 | ||||||
chr5:112997846 | C | T | 1 | a0001c0001t0111g0152 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.433-3238C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997846 | ||||||
chr5:112997849 | G | A | 6 | a0001c0001t0004g0271a0001c0001t0004g0281a0001c0001t0099g0246others(3): Show | 6 | NA18966.hp2 NA18985.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-3235G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997849 | ||||||
chr5:112997928 | TA | T | 4 | a0001c0001t0004g0003a0001c0001t0020g0003a0001c0001t0020g0279others(1): Show | 5 | NA18942.hp1 NA18948.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-3148delA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112997928 | |||||
chr5:112997975 | T | G | 1 | a0001c0001t0003g0146 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.433-3109T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997975 | ||||||
chr5:112998274 | ATTCCTGG others(20): Show |
A | 1 | a0001c0001t0003g0185 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.433-2807_433-2781d others(29): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112998274 | |||||
chr5:112998315 | G | A | 1 | a0001c0001t0012g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.433-2769G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112998315 | ||||||
chr5:112998445 | T | C | 259 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(256): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.433-2639T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112998445 | ||||||
chr5:112998490 | G | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(148): Show | 162 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.433-2594G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112998490 | ||||||
chr5:112998525 | G | A | 1 | a0001c0001t0043g0195 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.433-2559G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112998525 | ||||||
chr5:112998822 | T | G | 1 | a0001c0001t0101g0341 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.433-2262T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112998822 | ||||||
chr5:112998841 | C | T | 1 | a0001c0002t0052g0048 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.433-2243C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112998841 | ||||||
chr5:112998912 | T | A | 2 | a0001c0002t0039g0225a0001c0002t0114g0223 | 2 | HG02109.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.433-2172T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112998912 | ||||||
chr5:112999031 | T | G | 1 | a0001c0001t0001g0343 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.433-2053T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999031 | ||||||
chr5:112999160 | C | T | 260 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(257): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.433-1924C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999160 | ||||||
chr5:112999171 | A | C | 1 | a0001c0001t0001g0306 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.433-1913A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999171 | ||||||
chr5:112999279 | T | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(151): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.433-1805T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999279 | ||||||
chr5:112999454 | G | A | 3 | a0001c0004t0019g0020a0001c0004t0019g0134a0001c0004t0060g0131 | 3 | HG01891.hp1 HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.433-1630G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999454 | ||||||
chr5:112999476 | G | A | 7 | a0001c0001t0013g0147a0001c0001t0013g0153a0001c0001t0013g0154others(4): Show | 7 | HG01496.hp2 HG02055.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.433-1608G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999476 | ||||||
chr5:112999478 | G | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(151): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.433-1606G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999478 | ||||||
chr5:112999565 | A | G | 1 | a0001c0001t0020g0279 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.433-1519A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999565 | ||||||
chr5:112999625 | C | A | 1 | a0001c0001t0112g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.433-1459C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999625 | ||||||
chr5:112999626 | C | CT | 9 | a0001c0001t0003g0207a0001c0001t0005g0127a0001c0001t0005g0219others(6): Show | 9 | HG01243.hp2 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.433-1441dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112999626 | |||||
chr5:112999626 | CT | C | 18 | a0001c0001t0004g0280a0001c0001t0013g0147a0001c0001t0013g0153others(15): Show | 18 | HG01256.hp2 HG01496.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.433-1441delT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112999626 | |||||
chr5:112999651 | G | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(151): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.433-1433G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999651 | ||||||
chr5:112999953 | C | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(145): Show | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.433-1131C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999953 | ||||||
chr5:113000061 | C | CA | 66 | a0001c0001t0001g0343a0001c0001t0003g0144a0001c0001t0003g0145others(63): Show | 67 | HG00609.hp1 HG01106.hp1 HG01515.hp1 others(64): Show |
intron_variant | MODIFIER | c.433-1002dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000061 | |||||
chr5:113000061 | C | CAA | 12 | a0001c0001t0003g0174a0001c0001t0006g0137a0001c0001t0006g0138others(9): Show | 12 | HG02155.hp2 HG03490.hp2 HG03831.hp1 others(9): Show |
intron_variant | MODIFIER | c.433-1003_433-1002d others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000061 | |||||
chr5:113000061 | CA | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(140): Show | 154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.433-1002delA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000061 | |||||
chr5:113000061 | CAA | C | 7 | a0001c0001t0001g0262a0001c0001t0001g0303a0001c0001t0085g0307others(4): Show | 7 | HG01070.hp2 HG03225.hp1 NA18986.hp2 others(4): Show |
intron_variant | MODIFIER | c.433-1003_433-1002d others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000061 | |||||
chr5:113000155 | C | T | 4 | a0001c0001t0040g0333a0001c0001t0040g0334a0001c0001t0110g0332others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-929C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000155 | ||||||
chr5:113000167 | A | C | 1 | a0001c0001t0001g0230 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.433-917A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000167 | ||||||
chr5:113000318 | G | T | 155 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(152): Show | 166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.433-766G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000318 | ||||||
chr5:113000372 | T | G | 4 | a0001c0001t0040g0333a0001c0001t0040g0334a0001c0001t0110g0332others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-712T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000372 | ||||||
chr5:113000399 | T | TACAC | 14 | a0001c0002t0008g0053a0001c0002t0008g0055a0001c0002t0008g0068others(11): Show | 14 | HG00423.hp2 HG01928.hp1 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.433-662_433-659dup others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000399 | |||||
chr5:113000399 | T | TACACAC | 11 | a0001c0001t0012g0008a0001c0001t0012g0167a0001c0001t0012g0168others(8): Show | 12 | HG00621.hp1 HG01074.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.433-664_433-659dup others(6): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000399 | |||||
chr5:113000399 | TAC | T | 4 | a0001c0002t0002g0059a0001c0002t0002g0115a0001c0002t0002g0218others(1): Show | 4 | HG00733.hp2 HG01081.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-660_433-659del others(2): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000399 | |||||
chr5:113000406 | A | ACACACAC others(3): Show |
2 | a0001c0001t0006g0199a0001c0001t0006g0200 | 2 | NA18960.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.433-669_433-668ins others(10): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000406 | |||||
chr5:113000408 | A | ACACCCAC others(9): Show |
6 | a0001c0001t0005g0162a0001c0001t0011g0159a0001c0001t0011g0160others(3): Show | 6 | HG02258.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-673_433-672ins others(16): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000408 | |||||
chr5:113000420 | A | ACACACAC others(6): Show |
1 | a0001c0001t0003g0175 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.433-659_433-658ins others(13): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | |||||
chr5:113000420 | A | ACACACAC others(8): Show |
1 | a0001c0001t0015g0026 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.433-659_433-658ins others(15): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | |||||
chr5:113000420 | A | ACACACAC others(15): Show |
1 | a0001c0001t0112g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.433-659_433-658ins others(22): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | |||||
chr5:113000420 | A | ACACACAC others(9): Show |
1 | a0001c0001t0072g0342 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.433-659_433-658ins others(16): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | |||||
chr5:113000420 | A | ACACACAC others(11): Show |
3 | a0001c0001t0040g0333a0001c0001t0040g0334a0001c0001t0110g0332 | 3 | HG01070.hp1 HG01071.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.433-659_433-658ins others(18): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | |||||
chr5:113000420 | A | ACACACAC others(7): Show |
10 | a0001c0001t0003g0176a0001c0001t0013g0154a0001c0001t0015g0024others(7): Show | 11 | HG02257.hp2 HG02630.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.433-659_433-658ins others(14): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | |||||
chr5:113000420 | A | ACACACAC others(5): Show |
10 | a0001c0001t0013g0147a0001c0001t0013g0153a0001c0001t0013g0157others(7): Show | 10 | HG01496.hp2 HG02055.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-659_433-658ins others(12): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | |||||
chr5:113000420 | A | ACACACAC others(7): Show |
1 | a0001c0010t0070g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.433-659_433-658ins others(14): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | |||||
chr5:113000420 | A | ACACACAC others(3): Show |
40 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(37): Show | 40 | HG01106.hp1 HG01515.hp1 HG02155.hp2 others(37): Show |
intron_variant | MODIFIER | c.433-659_433-658ins others(10): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | |||||
chr5:113000420 | A | ACACACAC others(1): Show |
5 | a0001c0001t0022g0215a0001c0001t0022g0216a0001c0001t0022g0217others(2): Show | 5 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-659_433-658ins others(8): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | |||||
chr5:113000420 | A | ACACACAC others(3): Show |
1 | a0001c0001t0003g0169 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.433-659_433-658ins others(10): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | |||||
chr5:113000420 | A | ACACACC | 8 | a0001c0001t0001g0285a0001c0001t0003g0180a0001c0001t0003g0185others(5): Show | 8 | HG00621.hp2 HG02015.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.433-658_433-653dup others(6): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | |||||
chr5:113000420 | A | ACACACCC others(1): Show |
18 | a0001c0001t0007g0018a0001c0001t0007g0031a0001c0001t0007g0032others(15): Show | 18 | HG00609.hp1 HG02129.hp1 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.433-657_433-656ins others(8): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | |||||
chr5:113000420 | A | ACACC | 123 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(120): Show | 131 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.433-661_433-660ins others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | |||||
chr5:113000420 | A | ACC | 23 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(20): Show | 26 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.433-663_433-662ins others(2): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | |||||
chr5:113000420 | A | C | 40 | a0001c0001t0005g0127a0001c0001t0005g0162a0001c0001t0005g0219others(37): Show | 40 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.433-664A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000420 | ||||||
chr5:113000550 | G | A | 1 | a0001c0001t0016g0274 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.433-534G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000550 | ||||||
chr5:113000580 | A | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0263a0001c0001t0001g0298others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.433-504A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000580 | ||||||
chr5:113000606 | G | C | 1 | a0001c0002t0048g0052 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.433-478G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000606 | ||||||
chr5:113000680 | C | G | 10 | a0001c0001t0015g0024a0001c0001t0015g0025a0001c0001t0015g0026others(7): Show | 10 | HG01496.hp1 HG02257.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-404C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000680 | ||||||
chr5:113000759 | G | T | 1 | a0001c0001t0012g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.433-325G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000759 | ||||||
chr5:113000821 | T | G | 1 | a0001c0001t0112g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.433-263T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000821 | ||||||
chr5:113000844 | A | G | 6 | a0001c0001t0005g0162a0001c0001t0011g0159a0001c0001t0011g0160others(3): Show | 6 | HG02258.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-240A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000844 | ||||||
chr5:113000891 | C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(151): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.433-193C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000891 | ||||||
chr5:113000910 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.433-174G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000910 | ||||||
chr5:113000937 | T | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(151): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.433-147T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000937 | ||||||
chr5:113000993 | T | C | 3 | a0001c0001t0007g0041a0001c0001t0067g0042a0001c0001t0069g0040 | 3 | HG03209.hp2 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.433-91T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000993 | ||||||
chr5:113001308 | G | A | 1 | a0001c0001t0001g0294 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.586-49G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 5/10 | chr5 | 113001308 | ||||||
chr5:113001796 | T | G | 1 | a0001c0001t0003g0172 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.806+122T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113001796 | ||||||
chr5:113001958 | G | A | 1 | a0001c0002t0002g0021 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.806+284G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113001958 | ||||||
chr5:113002058 | T | A | 1 | a0001c0001t0003g0176 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.806+384T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113002058 | ||||||
chr5:113002162 | C | G | 2 | a0001c0002t0039g0225a0001c0002t0114g0223 | 2 | HG02109.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.806+488C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113002162 | ||||||
chr5:113002162 | C | T | 1 | a0001c0001t0006g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.806+488C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113002162 | ||||||
chr5:113002262 | G | A | 153 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(150): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.806+588G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113002262 | ||||||
chr5:113002422 | C | CA | 21 | a0001c0001t0001g0012a0001c0001t0001g0249a0001c0001t0001g0250others(18): Show | 22 | HG00621.hp2 HG00673.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.806+765dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 113002422 | |||||
chr5:113002422 | CA | C | 7 | a0001c0001t0001g0269a0001c0001t0003g0145a0001c0001t0068g0037others(4): Show | 7 | HG00609.hp2 HG01169.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.806+765delA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 113002422 | |||||
chr5:113002423 | A | G | 1 | a0001c0001t0077g0179 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.806+749A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113002423 | ||||||
chr5:113002714 | GC | G | 2 | a0001c0001t0003g0176a0001c0001t0032g0009 | 3 | HG03491.hp2 HG03492.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.806+1041delC | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113002714 | ||||||
chr5:113002729 | C | T | 1 | a0001c0001t0081g0233 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.806+1055C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113002729 | ||||||
chr5:113002773 | T | C | 3 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146 | 3 | HG03471.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.806+1099T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113002773 | ||||||
chr5:113003111 | C | T | 1 | a0001c0010t0070g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.807-831C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003111 | ||||||
chr5:113003164 | G | GGTC | 259 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(256): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.807-778_807-777ins others(3): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003164 | ||||||
chr5:113003165 | A | T | 259 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(256): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.807-777A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003165 | ||||||
chr5:113003167 | T | G | 259 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(256): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.807-775T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003167 | ||||||
chr5:113003220 | T | G | 2 | a0001c0002t0002g0046a0001c0002t0002g0051 | 2 | HG01346.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.807-722T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003220 | ||||||
chr5:113003242 | C | T | 6 | a0001c0001t0018g0228a0001c0001t0018g0312a0001c0001t0018g0330others(3): Show | 6 | HG01884.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.807-700C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003242 | ||||||
chr5:113003250 | A | G | 1 | a0001c0001t0112g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.807-692A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003250 | ||||||
chr5:113003351 | T | C | 14 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(11): Show | 17 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.807-591T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003351 | ||||||
chr5:113003701 | GA | G | 50 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(47): Show | 51 | HG01106.hp1 HG01515.hp1 HG02015.hp1 others(48): Show |
intron_variant | MODIFIER | c.807-233delA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 113003701 | |||||
chr5:113003712 | G | A | 1 | a0001c0001t0112g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.807-230G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003712 | ||||||
chr5:113003881 | G | T | 2 | a0001c0001t0003g0169a0001c0001t0003g0189 | 2 | HG01106.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.807-61G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003881 | ||||||
chr5:113004214 | T | C | 1 | a0001c0001t0080g0019 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.942+137T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113004214 | ||||||
chr5:113004462 | C | G | 1 | a0001c0001t0013g0154 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.942+385C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113004462 | ||||||
chr5:113004503 | C | T | 3 | a0001c0001t0022g0215a0001c0001t0022g0216a0001c0001t0022g0217 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.942+426C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113004503 | ||||||
chr5:113004674 | C | G | 3 | a0001c0001t0024g0166a0001c0001t0024g0201a0001c0001t0024g0202 | 3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.942+597C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113004674 | ||||||
chr5:113004794 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.942+717A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113004794 | ||||||
chr5:113004819 | T | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(148): Show | 162 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.942+742T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113004819 | ||||||
chr5:113004850 | A | G | 4 | a0001c0001t0040g0333a0001c0001t0040g0334a0001c0001t0110g0332others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.942+773A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113004850 | ||||||
chr5:113004952 | C | T | 1 | a0001c0002t0002g0057 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.942+875C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113004952 | ||||||
chr5:113004994 | G | A | 15 | a0001c0001t0017g0010a0001c0001t0017g0011a0001c0001t0017g0214others(12): Show | 18 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.942+917G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113004994 | ||||||
chr5:113005145 | C | CGTGTGTG others(1): Show |
6 | a0001c0001t0011g0159a0001c0001t0011g0160a0001c0001t0011g0163others(3): Show | 6 | HG01192.hp2 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.942+1073_942+1074i others(10): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005145 | |||||
chr5:113005145 | C | CGTGTGTG others(5): Show |
2 | a0001c0001t0033g0194a0001c0001t0033g0209 | 2 | NA18952.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.942+1073_942+1074i others(14): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005145 | |||||
chr5:113005145 | C | T | 1 | a0001c0002t0014g0107 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.942+1068C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005145 | ||||||
chr5:113005151 | G | GGTGTGGG others(9): Show |
1 | a0001c0001t0003g0177 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.942+1079_942+1080i others(18): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | |||||
chr5:113005151 | G | GGTGTGT | 77 | a0001c0002t0002g0001a0001c0002t0002g0021a0001c0002t0002g0058others(74): Show | 80 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.942+1087_942+1092d others(8): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | |||||
chr5:113005151 | G | GGTGTGTG others(5): Show |
147 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(144): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.942+1081_942+1082i others(14): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | |||||
chr5:113005151 | G | GGTGTGTG others(7): Show |
6 | a0001c0001t0001g0278a0001c0001t0005g0127a0001c0001t0005g0219others(3): Show | 6 | HG03130.hp2 HG03540.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.942+1081_942+1082i others(16): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | |||||
chr5:113005151 | G | GGTGTGTG others(3): Show |
6 | a0001c0001t0024g0166a0001c0001t0024g0201a0001c0001t0024g0202others(3): Show | 6 | HG01358.hp2 HG01516.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.942+1083_942+1092d others(12): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | |||||
chr5:113005151 | G | GGTGTGTG others(5): Show |
25 | a0001c0001t0007g0018a0001c0001t0007g0031a0001c0001t0007g0032others(22): Show | 26 | HG00609.hp1 HG01496.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.942+1081_942+1092d others(14): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | |||||
chr5:113005151 | G | GGTGTGTG others(7): Show |
49 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(46): Show | 49 | HG01496.hp1 HG02155.hp2 HG02257.hp2 others(46): Show |
intron_variant | MODIFIER | c.942+1079_942+1092d others(16): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | |||||
chr5:113005151 | G | GGTGTGTG others(9): Show |
11 | a0001c0001t0003g0169a0001c0001t0003g0171a0001c0001t0003g0185others(8): Show | 11 | HG01106.hp1 HG01515.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.942+1077_942+1092d others(18): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | |||||
chr5:113005151 | G | GGTGTGTG others(11): Show |
2 | a0001c0001t0003g0180a0001c0001t0012g0168 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.942+1075_942+1092d others(20): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | |||||
chr5:113005151 | G | GGTGTGTG others(13): Show |
9 | a0001c0001t0012g0008a0001c0001t0012g0148a0001c0001t0012g0167others(6): Show | 10 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.942+1092_942+1093i others(22): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | |||||
chr5:113005151 | G | T | 10 | a0001c0001t0005g0162a0001c0001t0011g0159a0001c0001t0011g0160others(7): Show | 10 | HG01192.hp2 HG02040.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.942+1074G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005151 | ||||||
chr5:113005157 | T | TGTGTGTG others(7): Show |
1 | a0001c0010t0070g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.942+1092_942+1093i others(16): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005157 | |||||
chr5:113005383 | T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0263a0001c0001t0001g0298others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.942+1306T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005383 | ||||||
chr5:113005389 | TG | T | 11 | a0001c0001t0015g0024a0001c0001t0015g0025a0001c0001t0015g0026others(8): Show | 11 | HG01496.hp1 HG02257.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.942+1314delG | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005389 | |||||
chr5:113005390 | G | T | 1 | a0001c0001t0001g0337 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.942+1313G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005390 | ||||||
chr5:113005551 | T | C | 156 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(153): Show | 167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.942+1474T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005551 | ||||||
chr5:113005701 | A | G | 5 | a0001c0001t0018g0228a0001c0001t0018g0312a0001c0001t0018g0330others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.942+1624A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005701 | ||||||
chr5:113005705 | A | G | 3 | a0001c0002t0002g0051a0001c0004t0019g0133a0001c0004t0062g0132 | 3 | HG00741.hp1 HG03195.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.942+1628A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005705 | ||||||
chr5:113005809 | A | G | 1 | a0001c0001t0045g0067 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.942+1732A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005809 | ||||||
chr5:113005894 | A | G | 1 | a0001c0001t0013g0153 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.942+1817A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005894 | ||||||
chr5:113005931 | G | A | 1 | a0001c0001t0003g0173 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.942+1854G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005931 | ||||||
chr5:113005941 | T | G | 3 | a0001c0001t0022g0215a0001c0001t0022g0216a0001c0001t0022g0217 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.942+1864T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005941 | ||||||
chr5:113005989 | G | C | 51 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(48): Show | 52 | HG01106.hp1 HG01515.hp1 HG02015.hp1 others(49): Show |
intron_variant | MODIFIER | c.942+1912G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005989 | ||||||
chr5:113006117 | C | CA | 57 | a0001c0001t0001g0235a0001c0001t0001g0285a0001c0001t0001g0287others(54): Show | 58 | HG00280.hp2 HG00609.hp1 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.943-1799dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113006117 | |||||
chr5:113006117 | C | CAA | 8 | a0001c0001t0001g0254a0001c0001t0001g0262a0001c0001t0011g0159others(5): Show | 8 | HG00408.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.943-1800_943-1799d others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113006117 | |||||
chr5:113006182 | T | C | 1 | a0001c0002t0002g0105 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.943-1756T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113006182 | ||||||
chr5:113006431 | A | G | 24 | a0001c0001t0007g0018a0001c0001t0007g0031a0001c0001t0007g0032others(21): Show | 25 | HG00609.hp1 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.943-1507A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113006431 | ||||||
chr5:113006585 | C | G | 59 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(56): Show | 60 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(57): Show |
intron_variant | MODIFIER | c.943-1353C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113006585 | ||||||
chr5:113006648 | CTATT | C | 6 | a0001c0001t0005g0162a0001c0001t0011g0159a0001c0001t0011g0160others(3): Show | 6 | HG02258.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.943-1285_943-1282d others(6): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113006648 | |||||
chr5:113006662 | T | G | 1 | a0001c0001t0074g0170 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.943-1276T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113006662 | ||||||
chr5:113006692 | A | G | 2 | a0001c0001t0038g0023a0001c0001t0038g0161 | 2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.943-1246A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113006692 | ||||||
chr5:113006727 | G | A | 3 | a0001c0001t0024g0166a0001c0001t0024g0201a0001c0001t0024g0202 | 3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.943-1211G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113006727 | ||||||
chr5:113007140 | T | A | 1 | a0001c0001t0022g0216 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.943-798T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007140 | ||||||
chr5:113007143 | T | C | 3 | a0001c0001t0040g0333a0001c0001t0040g0334a0001c0001t0110g0332 | 3 | HG01070.hp1 HG01071.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.943-795T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007143 | ||||||
chr5:113007243 | A | G | 1 | a0001c0001t0006g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.943-695A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007243 | ||||||
chr5:113007297 | C | G | 1 | a0001c0001t0001g0324 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.943-641C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007297 | ||||||
chr5:113007376 | ATTTC | A | 232 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(229): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.943-538_943-535del others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113007376 | |||||
chr5:113007396 | CTTTCT | C | 24 | a0001c0001t0001g0310a0001c0001t0007g0018a0001c0001t0007g0031others(21): Show | 25 | HG00609.hp1 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.943-538_943-534del others(5): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113007396 | |||||
chr5:113007591 | G | A | 3 | a0001c0001t0024g0166a0001c0001t0024g0201a0001c0001t0024g0202 | 3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.943-347G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007591 | ||||||
chr5:113007676 | C | T | 20 | a0001c0001t0005g0162a0001c0001t0011g0159a0001c0001t0011g0160others(17): Show | 20 | HG01496.hp1 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.943-262C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007676 | ||||||
chr5:113007690 | C | T | 1 | a0001c0001t0001g0328 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.943-248C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007690 | ||||||
chr5:113007712 | T | A | 10 | a0001c0001t0003g0169a0001c0001t0003g0180a0001c0001t0003g0185others(7): Show | 10 | HG01106.hp1 HG01515.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.943-226T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007712 | ||||||
chr5:113007847 | G | A | 260 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(257): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.943-91G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007847 | ||||||
chr5:113007876 | A | G | 1 | a0001c0001t0001g0288 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.943-62A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007876 | ||||||
chr5:113008097 | C | A | 1 | a0001c0001t0003g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1047+55C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008097 | ||||||
chr5:113008098 | A | G | 4 | a0001c0001t0001g0226a0001c0001t0021g0299a0001c0001t0021g0300others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.1047+56A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008098 | ||||||
chr5:113008162 | G | T | 2 | a0001c0001t0005g0127a0001c0001t0005g0219 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1047+120G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008162 | ||||||
chr5:113008181 | T | C | 2 | a0001c0001t0001g0255a0001c0001t0001g0339 | 2 | HG00738.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1047+139T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008181 | ||||||
chr5:113008190 | A | G | 2 | a0001c0001t0003g0176a0001c0001t0032g0009 | 3 | HG03491.hp2 HG03492.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1047+148A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008190 | ||||||
chr5:113008385 | G | A | 215 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(212): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1047+343G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008385 | ||||||
chr5:113008389 | A | G | 1 | a0001c0002t0048g0052 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1047+347A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008389 | ||||||
chr5:113008476 | C | CTGAAT | 259 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(256): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1047+434_1047+435i others(7): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008476 | ||||||
chr5:113008572 | A | C | 1 | a0001c0001t0030g0123 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1047+530A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008572 | ||||||
chr5:113008572 | A | G | 3 | a0001c0001t0022g0215a0001c0001t0022g0216a0001c0001t0022g0217 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1047+530A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008572 | ||||||
chr5:113008846 | T | C | 4 | a0001c0001t0012g0008a0001c0001t0012g0148a0001c0001t0012g0167others(1): Show | 5 | HG01074.hp2 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047+804T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008846 | ||||||
chr5:113008849 | C | CT | 78 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(75): Show | 79 | HG00639.hp2 HG01106.hp1 HG01243.hp1 others(76): Show |
intron_variant | MODIFIER | c.1047+820dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113008849 | |||||
chr5:113008958 | C | G | 1 | a0001c0001t0020g0279 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1047+916C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008958 | ||||||
chr5:113008958 | C | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(121): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1047+916C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008958 | ||||||
chr5:113009094 | C | T | 2 | a0001c0002t0039g0225a0001c0002t0114g0223 | 2 | HG02109.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1047+1052C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009094 | ||||||
chr5:113009134 | C | T | 6 | a0001c0001t0005g0162a0001c0001t0011g0159a0001c0001t0011g0160others(3): Show | 6 | HG02258.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1047+1092C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009134 | ||||||
chr5:113009255 | C | G | 5 | a0001c0001t0006g0137a0001c0001t0006g0138a0001c0001t0006g0140others(2): Show | 5 | HG02155.hp2 NA18948.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047+1213C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009255 | ||||||
chr5:113009268 | C | A | 257 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(254): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1047+1226C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009268 | ||||||
chr5:113009274 | T | A | 1 | a0001c0001t0001g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1047+1232T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009274 | ||||||
chr5:113009315 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG01081.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1047+1273C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009315 | ||||||
chr5:113009654 | A | AGAT | 59 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(56): Show | 60 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(57): Show |
intron_variant | MODIFIER | c.1048-1101_1048-109 others(7): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113009654 | |||||
chr5:113009698 | C | G | 59 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(56): Show | 60 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(57): Show |
intron_variant | MODIFIER | c.1048-1058C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009698 | ||||||
chr5:113009748 | CATTAT | C | 12 | a0001c0002t0008g0053a0001c0002t0008g0055a0001c0002t0008g0068others(9): Show | 12 | HG00423.hp2 HG01928.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1048-1004_1048-100 others(9): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113009748 | |||||
chr5:113009750 | T | A | 59 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(56): Show | 60 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(57): Show |
intron_variant | MODIFIER | c.1048-1006T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009750 | ||||||
chr5:113009759 | A | G | 60 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(57): Show | 61 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(58): Show |
intron_variant | MODIFIER | c.1048-997A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009759 | ||||||
chr5:113009856 | C | T | 6 | a0001c0001t0004g0271a0001c0001t0004g0281a0001c0001t0099g0246others(3): Show | 6 | NA18966.hp2 NA18985.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.1048-900C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009856 | ||||||
chr5:113009921 | C | CTTT | 57 | a0001c0001t0003g0145a0001c0001t0003g0146a0001c0001t0003g0169others(54): Show | 58 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(55): Show |
intron_variant | MODIFIER | c.1048-823_1048-821d others(5): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113009921 | |||||
chr5:113009969 | A | G | 1 | a0001c0002t0002g0054 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1048-787A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009969 | ||||||
chr5:113009977 | T | C | 1 | a0001c0001t0004g0271 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1048-779T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009977 | ||||||
chr5:113010034 | C | CT | 54 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(51): Show | 55 | HG01106.hp1 HG01515.hp1 HG02015.hp1 others(52): Show |
intron_variant | MODIFIER | c.1048-706dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113010034 | |||||
chr5:113010034 | C | CTT | 8 | a0001c0001t0003g0176a0001c0001t0013g0147a0001c0001t0013g0153others(5): Show | 8 | HG01496.hp2 HG02055.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1048-707_1048-706d others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113010034 | |||||
chr5:113010034 | CT | C | 6 | a0001c0001t0001g0310a0001c0001t0001g0325a0001c0001t0024g0201others(3): Show | 6 | HG00280.hp1 HG01167.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1048-706delT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113010034 | |||||
chr5:113010207 | A | AT | 39 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0316others(36): Show | 40 | HG00609.hp1 HG00621.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1048-530dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113010207 | |||||
chr5:113010207 | AT | A | 56 | a0001c0001t0001g0284a0001c0001t0003g0144a0001c0001t0003g0145others(53): Show | 57 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(54): Show |
intron_variant | MODIFIER | c.1048-530delT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113010207 | |||||
chr5:113010246 | A | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(147): Show | 161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1048-510A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010246 | ||||||
chr5:113010253 | C | A | 3 | a0001c0001t0024g0166a0001c0001t0024g0201a0001c0001t0024g0202 | 3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1048-503C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010253 | ||||||
chr5:113010339 | T | C | 59 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(56): Show | 60 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(57): Show |
intron_variant | MODIFIER | c.1048-417T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010339 | ||||||
chr5:113010365 | G | C | 1 | a0001c0001t0003g0192 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1048-391G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010365 | ||||||
chr5:113010389 | T | G | 59 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(56): Show | 60 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(57): Show |
intron_variant | MODIFIER | c.1048-367T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010389 | ||||||
chr5:113010486 | A | G | 59 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(56): Show | 60 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(57): Show |
intron_variant | MODIFIER | c.1048-270A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010486 | ||||||
chr5:113010719 | A | G | 2 | a0001c0001t0001g0308a0001c0001t0045g0067 | 2 | HG01358.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1048-37A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010719 | ||||||
chr5:113010734 | TG | T | 164 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(161): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1048-21delG | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010734 | ||||||
chr5:113010735 | G | T | 10 | a0001c0001t0005g0127a0001c0001t0005g0162a0001c0001t0005g0219others(7): Show | 10 | HG02258.hp1 HG02622.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1048-21G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010735 | ||||||
chr5:113010735 | GTT | G | 59 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(56): Show | 60 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(57): Show |
splice_region_variant&intron_variant | LOW | c.1048-8_1048-7delTT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113010735 | |||||
chr5:113010737 | T | G | 2 | a0001c0001t0007g0031a0001c0002t0102g0150 | 2 | HG01243.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1048-19T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010737 | ||||||
chr5:113010940 | G | A | 1 | a0001c0001t0001g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1099+133G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113010940 | ||||||
chr5:113010941 | T | G | 1 | a0001c0001t0001g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1099+134T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113010941 | ||||||
chr5:113011023 | C | A | 1 | a0001c0001t0001g0288 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1099+216C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113011023 | ||||||
chr5:113011211 | T | A | 1 | a0001c0007t0055g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1099+404T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113011211 | ||||||
chr5:113011337 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1099+530C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113011337 | ||||||
chr5:113011614 | A | T | 1 | a0001c0002t0002g0218 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1099+807A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113011614 | ||||||
chr5:113011785 | A | C | 1 | a0001c0001t0001g0276 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1099+978A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113011785 | ||||||
chr5:113011841 | G | A | 21 | a0001c0001t0007g0018a0001c0001t0007g0031a0001c0001t0007g0032others(18): Show | 21 | HG00609.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1099+1034G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113011841 | ||||||
chr5:113011966 | T | A | 1 | a0001c0001t0001g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1099+1159T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113011966 | ||||||
chr5:113011969 | C | A | 1 | a0001c0001t0001g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1099+1162C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113011969 | ||||||
chr5:113012010 | G | A | 1 | a0001c0001t0081g0233 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099+1203G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012010 | ||||||
chr5:113012013 | T | C | 209 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(206): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1099+1206T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012013 | ||||||
chr5:113012099 | T | C | 7 | a0001c0001t0013g0147a0001c0001t0013g0153a0001c0001t0013g0154others(4): Show | 7 | HG01496.hp2 HG02055.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1100-1222T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012099 | ||||||
chr5:113012131 | A | G | 153 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(150): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1100-1190A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012131 | ||||||
chr5:113012275 | A | T | 1 | a0001c0001t0001g0318 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1100-1046A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012275 | ||||||
chr5:113012281 | G | A | 3 | a0001c0001t0007g0041a0001c0001t0067g0042a0001c0001t0069g0040 | 3 | HG03209.hp2 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1100-1040G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012281 | ||||||
chr5:113012442 | A | C | 1 | a0001c0001t0083g0291 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1100-879A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012442 | ||||||
chr5:113012569 | GA | G | 3 | a0001c0001t0024g0166a0001c0001t0024g0201a0001c0001t0024g0202 | 3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1100-746delA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 113012569 | |||||
chr5:113012587 | T | C | 11 | a0001c0001t0005g0162a0001c0001t0011g0159a0001c0001t0011g0160others(8): Show | 11 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1100-734T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012587 | ||||||
chr5:113012600 | G | T | 57 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0146others(54): Show | 58 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(55): Show |
intron_variant | MODIFIER | c.1100-721G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012600 | ||||||
chr5:113012730 | G | A | 3 | a0001c0001t0022g0215a0001c0001t0022g0216a0001c0001t0022g0217 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1100-591G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012730 | ||||||
chr5:113012747 | C | G | 1 | a0001c0001t0007g0045 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1100-574C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012747 | ||||||
chr5:113012750 | T | A | 1 | a0001c0001t0005g0219 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1100-571T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012750 | ||||||
chr5:113012932 | A | G | 1 | a0001c0001t0004g0271 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1100-389A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012932 | ||||||
chr5:113013054 | G | A | 2 | a0001c0001t0021g0299a0001c0001t0021g0300 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1100-267G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113013054 | ||||||
chr5:113013094 | C | A | 1 | a0001c0002t0103g0149 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1100-227C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113013094 | ||||||
chr5:113013233 | T | TA | 3 | a0001c0001t0022g0215a0001c0001t0022g0216a0001c0001t0022g0217 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1100-86dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 113013233 |