geneid | 79871 |
---|---|
ensemblid | ENSG00000122484.9 |
hgncid | 25791 |
symbol | RPAP2 |
name | RNA polymerase II associated protein 2 |
refseq_nuc | NM_024813.3 |
refseq_prot | NP_079089.2 |
ensembl_nuc | ENST00000610020.2 |
ensembl_prot | ENSP00000476948.1 |
mane_status | MANE Select |
chr | chr1 |
start | 92299059 |
end | 92402056 |
strand | + |
ver | v1.2 |
region | chr1:92299059-92402056 |
region5000 | chr1:92294059-92407056 |
regionname0 | RPAP2_chr1_92299059_92402056 |
regionname5000 | RPAP2_chr1_92294059_92407056 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 613 | 185 | 70 | 49 | 30 | 10 | 24 | 18 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0002 | 0/0 | 613 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0003 | 0/0 | 613 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0004 | 0/0 | 613 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 7978 | 55 | 15 | 13 | 10 | 6 | 11 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0002 | 0/1 | 7978 | 34 | 1 | 15 | 8 | 1 | 8 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0003 | 0/0 | 7981 | 9 | 9 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0004 | 0/0 | 7980 | 8 | 8 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0005 | 0/0 | 7979 | 7 | 4 | 3 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0006 | 0/0 | 7979 | 6 | 6 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0007 | 0/0 | 7978 | 6 | 0 | 3 | 3 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0008 | 0/0 | 7977 | 6 | 0 | 2 | 1 | 3 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0009 | 0/0 | 7980 | 4 | 4 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0010 | 0/0 | 7978 | 4 | 0 | 4 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0011 | 0/0 | 7979 | 4 | 3 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0012 | 0/0 | 7978 | 3 | 0 | 3 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0013 | 0/0 | 7976 | 3 | 3 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0014 | 0/0 | 7976 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0015 | 0/0 | 7977 | 2 | 0 | 1 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0016 | 0/0 | 7979 | 2 | 0 | 2 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0017 | 0/0 | 7977 | 2 | 1 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0018 | 0/0 | 7978 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0019 | 0/0 | 7978 | 2 | 0 | 0 | 0 | 0 | 2 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0020 | 0/0 | 7978 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0021 | 0/0 | 7978 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0022 | 0/0 | 7978 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0023 | 0/0 | 7979 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0024 | 0/0 | 7980 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0025 | 0/0 | 7981 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0026 | 0/0 | 7977 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0027 | 0/0 | 7979 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0028 | 0/0 | 7819 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0029 | 0/0 | 7978 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0030 | 0/0 | 7978 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0031 | 0/0 | 7978 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0032 | 0/0 | 7978 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0033 | 0/0 | 7977 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0034 | 0/0 | 7978 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0035 | 0/0 | 7978 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0036 | 0/0 | 7978 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0037 | 0/0 | 7978 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0038 | 0/0 | 7978 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0039 | 0/0 | 7978 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0040 | 0/0 | 7978 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0041 | 0/0 | 7979 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0042 | 0/0 | 7979 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0043 | 1/0 | 7976 | 1 | 0 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0044 | 0/0 | 7977 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0045 | 0/0 | 7979 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0046 | 0/0 | 7979 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0047 | 0/0 | 7975 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0048 | 0/0 | 7977 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
c0049 | 0/0 | 7975 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 15061 | 31 | 1 | 14 | 6 | 1 | 8 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0002 | 0/0 | 15069 | 30 | 6 | 14 | 6 | 2 | 2 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0003 | 0/0 | 15064 | 12 | 6 | 1 | 2 | 2 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0004 | 0/0 | 15070 | 11 | 1 | 5 | 4 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0005 | 0/0 | 15060 | 8 | 8 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0006 | 0/0 | 15056 | 6 | 0 | 2 | 1 | 3 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0007 | 0/0 | 15060 | 4 | 4 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0008 | 0/0 | 15060 | 4 | 4 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0009 | 0/0 | 15061 | 4 | 4 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0010 | 0/0 | 15061 | 3 | 0 | 3 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0011 | 0/0 | 15057 | 3 | 3 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0012 | 0/0 | 15061 | 3 | 3 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0013 | 0/0 | 15065 | 2 | 1 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0014 | 0/0 | 15068 | 2 | 0 | 0 | 0 | 1 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0015 | 0/0 | 15064 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0016 | 0/0 | 15064 | 2 | 1 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0017 | 0/0 | 15060 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0018 | 0/0 | 15060 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0019 | 0/0 | 15061 | 2 | 0 | 2 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0020 | 0/0 | 15062 | 2 | 0 | 2 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0021 | 0/0 | 15054 | 2 | 1 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0022 | 0/0 | 15054 | 2 | 0 | 2 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0023 | 0/0 | 15056 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0024 | 0/0 | 15061 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0025 | 1/0 | 15061 | 1 | 0 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0026 | 0/0 | 15069 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0027 | 0/0 | 15064 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0028 | 0/0 | 15064 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0029 | 0/0 | 15063 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0030 | 0/0 | 15063 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0031 | 0/0 | 15069 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0032 | 0/0 | 15065 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0033 | 0/0 | 15072 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0034 | 0/0 | 15066 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0035 | 0/0 | 15069 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0036 | 0/0 | 15069 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0037 | 0/0 | 15069 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0038 | 0/0 | 15071 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0039 | 0/0 | 15071 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0040 | 0/0 | 15070 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0041 | 0/0 | 15036 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0042 | 0/0 | 15066 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0043 | 0/0 | 15066 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0044 | 0/0 | 15064 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0045 | 0/0 | 15069 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0046 | 0/0 | 15065 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0047 | 0/0 | 15064 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0048 | 0/0 | 15064 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0049 | 0/0 | 15065 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0050 | 0/0 | 15066 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0051 | 0/0 | 15072 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0052 | 0/0 | 15061 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0053 | 0/0 | 15061 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0054 | 0/0 | 15062 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0055 | 0/0 | 15060 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0056 | 0/0 | 15069 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0057 | 0/0 | 15060 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0058 | 0/0 | 15063 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0059 | 0/0 | 15061 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0060 | 0/0 | 15061 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0061 | 0/0 | 15061 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0062 | 0/0 | 15061 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0063 | 0/0 | 15061 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0064 | 0/0 | 15062 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0065 | 0/0 | 15061 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0066 | 0/0 | 15061 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0067 | 0/0 | 15060 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0068 | 0/0 | 15061 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0069 | 0/0 | 15058 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0070 | 0/0 | 15058 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0071 | 0/0 | 15054 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0072 | 0/0 | 15062 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0073 | 0/0 | 15057 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
t0074 | 0/0 | 15061 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0020 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0185 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 7978 | 55 | 15 | 13 | 10 | 6 | 11 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0002 | 0/1 | 7978 | 34 | 1 | 15 | 8 | 1 | 8 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0003 | 0/0 | 7981 | 9 | 9 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0004 | 0/0 | 7980 | 8 | 8 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0005 | 0/0 | 7979 | 7 | 4 | 3 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0006 | 0/0 | 7979 | 6 | 6 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0007 | 0/0 | 7978 | 6 | 0 | 3 | 3 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0008 | 0/0 | 7977 | 6 | 0 | 2 | 1 | 3 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0009 | 0/0 | 7980 | 4 | 4 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0010 | 0/0 | 7978 | 4 | 0 | 4 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0011 | 0/0 | 7979 | 4 | 3 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0012 | 0/0 | 7978 | 3 | 0 | 3 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0014 | 0/0 | 7976 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0015 | 0/0 | 7977 | 2 | 0 | 1 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0016 | 0/0 | 7979 | 2 | 0 | 2 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0017 | 0/0 | 7977 | 2 | 1 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0018 | 0/0 | 7978 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0019 | 0/0 | 7978 | 2 | 0 | 0 | 0 | 0 | 2 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0020 | 0/0 | 7978 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0021 | 0/0 | 7978 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0022 | 0/0 | 7978 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0023 | 0/0 | 7979 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0024 | 0/0 | 7980 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0025 | 0/0 | 7981 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0027 | 0/0 | 7979 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0028 | 0/0 | 7819 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0029 | 0/0 | 7978 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0030 | 0/0 | 7978 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0031 | 0/0 | 7978 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0032 | 0/0 | 7978 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0033 | 0/0 | 7977 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0034 | 0/0 | 7978 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0035 | 0/0 | 7978 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0036 | 0/0 | 7978 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0037 | 0/0 | 7978 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0038 | 0/0 | 7978 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0039 | 0/0 | 7978 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0040 | 0/0 | 7978 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0041 | 0/0 | 7979 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0042 | 0/0 | 7979 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0043 | 1/0 | 7976 | 1 | 0 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0044 | 0/0 | 7977 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0045 | 0/0 | 7979 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0046 | 0/0 | 7979 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0002c0013 | 0/0 | 7976 | 3 | 3 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0002c0047 | 0/0 | 7975 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0002c0048 | 0/0 | 7977 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0003c0049 | 0/0 | 7975 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0004c0026 | 0/0 | 7977 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 23046 | 19 | 3 | 9 | 4 | 2 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0003 | 0/0 | 23041 | 8 | 4 | 1 | 0 | 2 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0004 | 0/0 | 23047 | 5 | 1 | 2 | 1 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0013 | 0/0 | 23042 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0014 | 0/0 | 23045 | 2 | 0 | 0 | 0 | 1 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0015 | 0/0 | 23041 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0016 | 0/0 | 23041 | 2 | 1 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0026 | 0/0 | 23046 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0027 | 0/0 | 23041 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0028 | 0/0 | 23041 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0032 | 0/0 | 23042 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0035 | 0/0 | 23046 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0036 | 0/0 | 23046 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0037 | 0/0 | 23046 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0039 | 0/0 | 23048 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0040 | 0/0 | 23047 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0042 | 0/0 | 23043 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0043 | 0/0 | 23043 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0044 | 0/0 | 23041 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0045 | 0/0 | 23046 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0049 | 0/0 | 23042 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0050 | 0/0 | 23043 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0001t0056 | 0/0 | 23046 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0002t0001 | 0/1 | 23038 | 27 | 0 | 13 | 6 | 1 | 6 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0002t0019 | 0/0 | 23038 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0002t0059 | 0/0 | 23038 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0002t0060 | 0/0 | 23038 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0002t0062 | 0/0 | 23038 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0002t0063 | 0/0 | 23038 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0002t0065 | 0/0 | 23038 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0002t0066 | 0/0 | 23038 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0003t0009 | 0/0 | 23041 | 4 | 4 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0003t0012 | 0/0 | 23041 | 3 | 3 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0003t0072 | 0/0 | 23042 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0003t0074 | 0/0 | 23041 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0004t0008 | 0/0 | 23039 | 3 | 3 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0004t0017 | 0/0 | 23039 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0004t0052 | 0/0 | 23040 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0004t0053 | 0/0 | 23040 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0004t0067 | 0/0 | 23039 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0005t0021 | 0/0 | 23032 | 2 | 1 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0005t0022 | 0/0 | 23032 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0005t0023 | 0/0 | 23034 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0005t0071 | 0/0 | 23032 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0005t0073 | 0/0 | 23035 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0006t0005 | 0/0 | 23038 | 6 | 6 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0007t0004 | 0/0 | 23047 | 4 | 0 | 2 | 2 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0007t0031 | 0/0 | 23046 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0007t0051 | 0/0 | 23049 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0008t0006 | 0/0 | 23032 | 6 | 0 | 2 | 1 | 3 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0009t0007 | 0/0 | 23039 | 3 | 3 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0009t0024 | 0/0 | 23040 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0010t0002 | 0/0 | 23046 | 4 | 0 | 4 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0011t0002 | 0/0 | 23047 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0011t0003 | 0/0 | 23042 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0011t0004 | 0/0 | 23048 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0011t0038 | 0/0 | 23049 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0012t0010 | 0/0 | 23038 | 3 | 0 | 3 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0014t0029 | 0/0 | 23038 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0014t0030 | 0/0 | 23038 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0015t0001 | 0/0 | 23037 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0015t0019 | 0/0 | 23037 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0016t0020 | 0/0 | 23040 | 2 | 0 | 2 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0017t0002 | 0/0 | 23045 | 2 | 1 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0018t0003 | 0/0 | 23041 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0019t0013 | 0/0 | 23042 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0019t0034 | 0/0 | 23043 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0020t0018 | 0/0 | 23037 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0021t0022 | 0/0 | 23031 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0022t0005 | 0/0 | 23037 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0023t0005 | 0/0 | 23038 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0024t0007 | 0/0 | 23039 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0025t0008 | 0/0 | 23040 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0027t0046 | 0/0 | 23043 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0028t0061 | 0/0 | 22879 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0029t0064 | 0/0 | 23039 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0030t0001 | 0/0 | 23038 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0031t0001 | 0/0 | 23038 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0032t0033 | 0/0 | 23049 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0033t0047 | 0/0 | 23040 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0034t0002 | 0/0 | 23046 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0035t0002 | 0/0 | 23046 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0036t0041 | 0/0 | 23013 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0037t0003 | 0/0 | 23041 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0038t0048 | 0/0 | 23041 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0039t0002 | 0/0 | 23046 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0040t0002 | 0/0 | 23046 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0041t0004 | 0/0 | 23048 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0042t0058 | 0/0 | 23041 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0043t0025 | 1/0 | 23036 | 1 | 0 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0044t0057 | 0/0 | 23036 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0045t0054 | 0/0 | 23040 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0001c0046t0055 | 0/0 | 23038 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0002c0013t0011 | 0/0 | 23032 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0002c0013t0068 | 0/0 | 23036 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0002c0047t0069 | 0/0 | 23032 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0002c0048t0011 | 0/0 | 23033 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0003c0049t0070 | 0/0 | 23032 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
a0004c0026t0001 | 0/0 | 23037 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | copy fasta | chr1 | 92294059 | 92407056 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0004g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0013g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0014g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0014g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0015g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0015g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0016g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0016g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0026g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0027g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0028g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0032g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0035g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0036g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0037g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0039g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0040g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0042g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0043g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0044g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0045g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0049g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0050g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0001t0056g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0020 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0019g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0059g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0060g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0062g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0063g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0065g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0002t0066g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0003t0009g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0003t0009g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0003t0012g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0003t0012g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0003t0012g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0003t0072g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0003t0074g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0004t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0004t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0004t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0004t0017g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0004t0017g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0004t0052g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0004t0053g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0004t0067g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0005t0021g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0005t0021g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0005t0022g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0005t0023g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0005t0023g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0005t0071g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0005t0073g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0006t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0006t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0006t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0006t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0006t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0006t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0007t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0007t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0007t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0007t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0007t0031g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0007t0051g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0008t0006g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0008t0006g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0008t0006g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0008t0006g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0008t0006g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0008t0006g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0009t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0009t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0009t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0009t0024g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0010t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0010t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0010t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0010t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0011t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0011t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0011t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0011t0038g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0012t0010g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0012t0010g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0012t0010g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0014t0029g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0014t0030g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0015t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0015t0019g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0016t0020g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0016t0020g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0017t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0017t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0018t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0018t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0019t0013g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0019t0034g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0020t0018g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0020t0018g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0021t0022g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0022t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0023t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0024t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0025t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0027t0046g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0028t0061g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0029t0064g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0030t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0031t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0032t0033g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0033t0047g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0034t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0035t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0036t0041g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0037t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0038t0048g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0039t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0040t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0041t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0042t0058g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0043t0025g0185 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0044t0057g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0045t0054g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0001c0046t0055g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0002c0013t0011g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0002c0013t0011g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0002c0013t0068g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0002c0047t0069g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0002c0048t0011g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0003c0049t0070g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
a0004c0026t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0044 | g0082 | EUR | GBR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG00099 | hp2 | a0001 | c0008 | t0006 | g0058 | EUR | GBR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0065 | EUR | FIN | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG00280 | hp2 | a0001 | c0008 | t0006 | g0014 | EUR | FIN | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | CHS | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG00423 | hp2 | a0001 | c0008 | t0006 | g0013 | EAS | CHS | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG00438 | hp1 | a0001 | c0002 | t0065 | g0023 | EAS | CHS | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG00438 | hp2 | a0001 | c0011 | t0004 | g0090 | EAS | CHS | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG00639 | hp1 | a0001 | c0008 | t0006 | g0057 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG00642 | hp1 | a0001 | c0016 | t0020 | g0106 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG00642 | hp2 | a0001 | c0041 | t0004 | g0100 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG00741 | hp1 | a0001 | c0016 | t0020 | g0135 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG00741 | hp2 | a0001 | c0012 | t0010 | g0027 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01069 | hp1 | a0001 | c0015 | t0019 | g0035 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01069 | hp2 | a0001 | c0005 | t0022 | g0150 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01070 | hp2 | a0001 | c0017 | t0002 | g0068 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01081 | hp1 | a0001 | c0010 | t0002 | g0076 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01081 | hp2 | a0001 | c0005 | t0021 | g0153 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01106 | hp1 | a0001 | c0007 | t0004 | g0132 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01106 | hp2 | a0001 | c0002 | t0059 | g0047 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01109 | hp1 | a0001 | c0005 | t0073 | g0155 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01168 | hp1 | a0001 | c0021 | t0022 | g0151 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01168 | hp2 | a0001 | c0012 | t0010 | g0039 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01169 | hp1 | a0001 | c0012 | t0010 | g0037 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01169 | hp2 | a0001 | c0001 | t0037 | g0115 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0136 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01192 | hp1 | a0001 | c0002 | t0019 | g0030 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01255 | hp2 | a0001 | c0007 | t0031 | g0105 | AMR | CLM | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01256 | hp1 | a0004 | c0026 | t0001 | g0029 | AMR | CLM | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | CLM | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | CLM | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | CLM | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01261 | hp2 | a0001 | c0010 | t0002 | g0083 | AMR | CLM | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01346 | hp1 | a0001 | c0010 | t0002 | g0081 | AMR | CLM | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | CLM | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | CLM | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | CLM | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01516 | hp2 | a0001 | c0008 | t0006 | g0059 | EUR | IBS | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01517 | hp1 | a0001 | c0001 | t0014 | g0110 | EUR | IBS | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01884 | hp1 | a0001 | c0005 | t0071 | g0157 | AFR | ACB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0072 | AFR | ACB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01891 | hp1 | a0001 | c0033 | t0047 | g0060 | AFR | ACB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01891 | hp2 | a0001 | c0003 | t0012 | g0145 | AFR | ACB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | PEL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01978 | hp1 | a0001 | c0007 | t0004 | g0127 | AMR | PEL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0048 | AMR | PEL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | KHV | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02040 | hp2 | a0001 | c0001 | t0035 | g0109 | EAS | KHV | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02055 | hp1 | a0001 | c0004 | t0052 | g0166 | AFR | ACB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02055 | hp2 | a0001 | c0003 | t0072 | g0149 | AFR | ACB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02135 | hp1 | a0001 | c0001 | t0036 | g0187 | EAS | KHV | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | KHV | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02145 | hp1 | a0001 | c0011 | t0002 | g0130 | AFR | ACB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02145 | hp2 | a0001 | c0020 | t0018 | g0161 | AFR | ACB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0052 | AMR | PEL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02148 | hp2 | a0001 | c0010 | t0002 | g0124 | AMR | PEL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02257 | hp1 | a0001 | c0001 | t0049 | g0070 | AFR | ACB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02257 | hp2 | a0001 | c0002 | t0062 | g0045 | AFR | ACB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02258 | hp1 | a0001 | c0001 | t0016 | g0075 | AFR | ACB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02258 | hp2 | a0001 | c0009 | t0007 | g0173 | AFR | ACB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02280 | hp1 | a0001 | c0003 | t0009 | g0147 | AFR | ACB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02280 | hp2 | a0001 | c0004 | t0053 | g0167 | AFR | ACB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | PEL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02300 | hp2 | a0001 | c0008 | t0006 | g0056 | AMR | PEL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02622 | hp1 | a0001 | c0005 | t0023 | g0156 | AFR | GWD | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02622 | hp2 | a0001 | c0001 | t0015 | g0139 | AFR | GWD | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02630 | hp1 | a0002 | c0048 | t0011 | g0007 | AFR | GWD | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02630 | hp2 | a0001 | c0006 | t0005 | g0183 | AFR | GWD | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02647 | hp2 | a0001 | c0006 | t0005 | g0179 | AFR | GWD | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0053 | SAS | PJL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02698 | hp2 | a0001 | c0001 | t0042 | g0074 | SAS | PJL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02723 | hp1 | a0002 | c0013 | t0011 | g0011 | AFR | GWD | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02723 | hp2 | a0001 | c0009 | t0007 | g0175 | AFR | GWD | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02735 | hp1 | a0001 | c0001 | t0016 | g0086 | SAS | PJL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02735 | hp2 | a0001 | c0001 | t0039 | g0087 | SAS | PJL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02738 | hp1 | a0001 | c0019 | t0034 | g0088 | SAS | PJL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02738 | hp2 | a0001 | c0001 | t0032 | g0091 | SAS | PJL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02809 | hp1 | a0001 | c0022 | t0005 | g0177 | AFR | GWD | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02809 | hp2 | a0001 | c0017 | t0002 | g0101 | AFR | GWD | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02818 | hp1 | a0001 | c0023 | t0005 | g0181 | AFR | GWD | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | GWD | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02922 | hp1 | a0001 | c0014 | t0030 | g0015 | AFR | ESN | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02922 | hp2 | a0003 | c0049 | t0070 | g0009 | AFR | ESN | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02970 | hp1 | a0001 | c0006 | t0005 | g0180 | AFR | ESN | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02970 | hp2 | a0001 | c0001 | t0028 | g0144 | AFR | ESN | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0116 | AFR | ESN | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02976 | hp2 | a0001 | c0004 | t0067 | g0171 | AFR | ESN | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03041 | hp1 | a0001 | c0009 | t0007 | g0172 | AFR | GWD | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | GWD | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03098 | hp1 | a0001 | c0001 | t0013 | g0073 | AFR | MSL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03098 | hp2 | a0001 | c0006 | t0005 | g0184 | AFR | MSL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03130 | hp1 | a0001 | c0045 | t0054 | g0158 | AFR | ESN | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | ESN | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03139 | hp1 | a0001 | c0038 | t0048 | g0098 | AFR | ESN | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03139 | hp2 | a0001 | c0003 | t0012 | g0001 | AFR | ESN | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | ESN | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03195 | hp2 | a0001 | c0044 | t0057 | g0159 | AFR | ESN | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03209 | hp1 | a0001 | c0011 | t0038 | g0094 | AFR | MSL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03209 | hp2 | a0001 | c0009 | t0024 | g0174 | AFR | MSL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03225 | hp1 | a0001 | c0046 | t0055 | g0162 | AFR | MSL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03225 | hp2 | a0001 | c0042 | t0058 | g0061 | AFR | MSL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03453 | hp1 | a0001 | c0001 | t0015 | g0138 | AFR | MSL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03453 | hp2 | a0001 | c0006 | t0005 | g0178 | AFR | MSL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03486 | hp1 | a0001 | c0037 | t0003 | g0140 | AFR | MSL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03486 | hp2 | a0002 | c0047 | t0069 | g0010 | AFR | MSL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03491 | hp1 | a0001 | c0015 | t0001 | g0025 | SAS | PJL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03491 | hp2 | a0001 | c0001 | t0014 | g0078 | SAS | PJL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0017 | SAS | PJL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03516 | hp1 | a0001 | c0024 | t0007 | g0176 | AFR | ESN | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03516 | hp2 | a0001 | c0027 | t0046 | g0117 | AFR | ESN | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03540 | hp1 | a0001 | c0005 | t0023 | g0152 | AFR | GWD | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03540 | hp2 | a0001 | c0005 | t0021 | g0154 | AFR | GWD | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0021 | SAS | PJL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0079 | SAS | PJL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03831 | hp1 | a0001 | c0034 | t0002 | g0128 | SAS | BEB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03831 | hp2 | a0001 | c0002 | t0060 | g0042 | SAS | BEB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03942 | hp1 | a0001 | c0002 | t0066 | g0033 | SAS | BEB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03942 | hp2 | a0001 | c0001 | t0026 | g0129 | SAS | BEB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG04115 | hp1 | a0001 | c0001 | t0043 | g0084 | SAS | STU | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0028 | SAS | STU | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0103 | SAS | BEB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0032 | SAS | BEB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG04199 | hp1 | a0001 | c0001 | t0045 | g0142 | SAS | STU | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG04199 | hp2 | a0001 | c0019 | t0013 | g0126 | SAS | STU | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG04204 | hp1 | a0001 | c0030 | t0001 | g0018 | SAS | STU | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0040 | SAS | STU | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | YRI | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA18522 | hp2 | a0001 | c0028 | t0061 | g0036 | AFR | YRI | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA18612 | hp1 | a0001 | c0039 | t0002 | g0123 | EAS | CHB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA18906 | hp1 | a0001 | c0014 | t0029 | g0016 | AFR | YRI | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA18906 | hp2 | a0001 | c0003 | t0009 | g0001 | AFR | YRI | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA18942 | hp1 | a0001 | c0001 | t0056 | g0097 | EAS | JPT | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA18970 | hp2 | a0001 | c0001 | t0027 | g0122 | EAS | JPT | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA18979 | hp1 | a0001 | c0018 | t0003 | g0118 | EAS | JPT | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA18979 | hp2 | a0001 | c0040 | t0002 | g0119 | EAS | JPT | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA18982 | hp1 | a0001 | c0001 | t0040 | g0104 | EAS | JPT | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA18982 | hp2 | a0001 | c0029 | t0064 | g0043 | EAS | JPT | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA19001 | hp1 | a0001 | c0036 | t0041 | g0095 | EAS | JPT | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA19001 | hp2 | a0001 | c0007 | t0004 | g0067 | EAS | JPT | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA19012 | hp1 | a0001 | c0007 | t0051 | g0099 | EAS | JPT | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA19030 | hp1 | a0001 | c0004 | t0008 | g0163 | AFR | LWK | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA19030 | hp2 | a0001 | c0003 | t0074 | g0148 | AFR | LWK | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA19043 | hp1 | a0001 | c0025 | t0008 | g0170 | AFR | LWK | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA19043 | hp2 | a0001 | c0011 | t0003 | g0089 | AFR | LWK | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA19058 | hp2 | a0001 | c0032 | t0033 | g0134 | EAS | JPT | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA19062 | hp1 | a0001 | c0007 | t0004 | g0102 | EAS | JPT | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA19087 | hp1 | a0001 | c0018 | t0003 | g0085 | EAS | JPT | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA19087 | hp2 | a0001 | c0002 | t0063 | g0055 | EAS | JPT | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA19240 | hp1 | a0001 | c0003 | t0012 | g0146 | AFR | YRI | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA19240 | hp2 | a0001 | c0004 | t0017 | g0165 | AFR | YRI | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA20129 | hp1 | a0001 | c0006 | t0005 | g0182 | AFR | ASW | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA20129 | hp2 | a0001 | c0003 | t0009 | g0001 | AFR | ASW | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0046 | EUR | TSI | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0125 | EUR | TSI | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | CLM | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02109 | hp1 | a0001 | c0004 | t0017 | g0164 | AFR | ACB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02109 | hp2 | a0002 | c0013 | t0068 | g0008 | AFR | ACB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02486 | hp1 | a0001 | c0001 | t0050 | g0112 | AFR | ACB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG02486 | hp2 | a0001 | c0020 | t0018 | g0160 | AFR | ACB | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03471 | hp1 | a0002 | c0013 | t0011 | g0012 | AFR | MSL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG03471 | hp2 | a0001 | c0035 | t0002 | g0121 | AFR | MSL | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG06807 | hp1 | a0001 | c0003 | t0009 | g0001 | AFR | USA | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
HG06807 | hp2 | a0001 | c0004 | t0008 | g0168 | AFR | USA | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA20300 | hp1 | a0001 | c0031 | t0001 | g0064 | AFR | USA | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
NA20300 | hp2 | a0001 | c0004 | t0008 | g0169 | AFR | USA | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0020 | REF | REF | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
homoSapiens_grch38 | hp1 | a0001 | c0043 | t0025 | g0185 | REF | REF | RPAP2_chr1_92294059_92407056 | RPAP2 | chr1 | 92294059 | 92407056 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:92304004
|
A | G | 1 | a0003 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.262A>G | p.Ser88Gly | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 4/13 | 277/16899 | 262/1839 | 88/612 | chr1 | 92304004 | ||
chr1:92323852
|
C | T | 2 | a0002a0003 | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
missense_variant | MODERATE | c.932C>T | p.Ala311Val | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/13 | 947/16899 | 932/1839 | 311/612 | chr1 | 92323852 | ||
chr1:92380765
|
G | A | 1 | a0004 | 1 | HG01256.hp1 | missense_variant | MODERATE | c.1730G>A | p.Gly577Asp | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/13 | 1745/16899 | 1730/1839 | 577/612 | chr1 | 92380765 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:92300204
|
G | A | 3 | a0001c0003a0001c0005a0001c0021 | 17 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(14): Show |
synonymous_variant | LOW | c.84G>A | p.Gln28Gln | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 2/13 | 99/16899 | 84/1839 | 28/612 | chr1 | 92300204 | ||
chr1:92323748
|
T | C | 7 | a0001c0004a0001c0006a0001c0009others(4): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
synonymous_variant | LOW | c.828T>C | p.Asp276Asp | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/13 | 843/16899 | 828/1839 | 276/612 | chr1 | 92323748 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:92387069
|
A | G | 10 | a0001c0003t0009a0001c0003t0012a0001c0003t0072others(7): Show | 17 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*58A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 58 | chr1 | 92387069 | |||||
chr1:92387198
|
A | G | 5 | a0001c0003t0009a0001c0003t0012a0001c0003t0072others(2): Show | 10 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*187A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 187 | chr1 | 92387198 | |||||
chr1:92387280
|
T | A | 10 | a0001c0003t0009a0001c0003t0012a0001c0003t0072others(7): Show | 17 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*269T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 269 | chr1 | 92387280 | |||||
chr1:92387363
|
A | G | 1 | a0003c0049t0070 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*352A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 352 | chr1 | 92387363 | |||||
chr1:92387373
|
G | A | 3 | a0001c0009t0007a0001c0009t0024a0001c0024t0007 | 5 | HG02258.hp2 HG02723.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*362G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 362 | chr1 | 92387373 | |||||
chr1:92387621
|
C | G | 1 | a0001c0003t0074 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*610C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 610 | chr1 | 92387621 | |||||
chr1:92387694
|
A | G | 5 | a0002c0013t0011a0002c0013t0068a0002c0047t0069others(2): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*683A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 683 | chr1 | 92387694 | |||||
chr1:92387862
|
C | T | 1 | a0001c0004t0067 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*851C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 851 | chr1 | 92387862 | |||||
chr1:92388221
|
A | G | 17 | a0001c0002t0001a0001c0002t0019a0001c0002t0059others(14): Show | 46 | HG00438.hp1 HG00642.hp1 HG00741.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1210A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 1210 | chr1 | 92388221 | |||||
chr1:92388229
|
T | G | 1 | a0001c0002t0059 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1218T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 1218 | chr1 | 92388229 | |||||
chr1:92388284
|
T | C | 1 | a0001c0002t0060 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1273T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 1273 | chr1 | 92388284 | |||||
chr1:92388591
|
G | T | 1 | a0001c0003t0012 | 3 | HG01891.hp2 HG03139.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1580G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 1580 | chr1 | 92388591 | |||||
chr1:92388744
|
C | T | 1 | a0001c0042t0058 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1733C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 1733 | chr1 | 92388744 | |||||
chr1:92388772
|
G | A | 5 | a0001c0005t0021a0001c0005t0022a0001c0005t0023others(2): Show | 7 | HG01069.hp2 HG01081.hp2 HG01168.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1761G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 1761 | chr1 | 92388772 | |||||
chr1:92388811
|
C | G | 5 | a0001c0005t0021a0001c0005t0022a0001c0005t0023others(2): Show | 7 | HG01069.hp2 HG01081.hp2 HG01168.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1800C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 1800 | chr1 | 92388811 | |||||
chr1:92389064
|
C | T | 1 | a0001c0044t0057 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2053C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 2053 | chr1 | 92389064 | |||||
chr1:92389106
|
C | T | 97 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(94): Show | 185 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*2095C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 2095 | chr1 | 92389106 | |||||
chr1:92389199
|
A | T | 1 | a0001c0012t0010 | 3 | HG00741.hp2 HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2188A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 2188 | chr1 | 92389199 | |||||
chr1:92389323
|
A | G | 1 | a0001c0002t0066 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2312A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 2312 | chr1 | 92389323 | |||||
chr1:92389494
|
G | A | 1 | a0001c0001t0026 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2483G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 2483 | chr1 | 92389494 | |||||
chr1:92389597
|
A | G | 1 | a0001c0005t0073 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2586A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 2586 | chr1 | 92389597 | |||||
chr1:92389730
|
G | A | 2 | a0001c0005t0021a0001c0005t0071 | 3 | HG01081.hp2 HG01884.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2719G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 2719 | chr1 | 92389730 | |||||
chr1:92389814
|
A | G | 1 | a0001c0001t0056 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2803A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 2803 | chr1 | 92389814 | |||||
chr1:92390064
|
A | G | 26 | a0001c0003t0009a0001c0003t0012a0001c0003t0072others(23): Show | 44 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*3053A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 3053 | chr1 | 92390064 | |||||
chr1:92390255
|
A | G | 1 | a0001c0007t0051 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3244A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 3244 | chr1 | 92390255 | |||||
chr1:92390490
|
T | C | 1 | a0001c0001t0027 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3479T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 3479 | chr1 | 92390490 | |||||
chr1:92390519
|
G | A | 1 | a0001c0028t0061 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3508G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 3508 | chr1 | 92390519 | |||||
chr1:92390602
|
A | G | 17 | a0001c0002t0001a0001c0002t0019a0001c0002t0059others(14): Show | 46 | HG00438.hp1 HG00642.hp1 HG00741.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*3591A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 3591 | chr1 | 92390602 | |||||
chr1:92390622
|
C | T | 1 | a0001c0007t0051 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3611C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 3611 | chr1 | 92390622 | |||||
chr1:92390693
|
T | C | 1 | a0001c0001t0028 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3682T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 3682 | chr1 | 92390693 | |||||
chr1:92390820
|
G | C | 2 | a0001c0014t0029a0001c0014t0030 | 2 | HG02922.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3809G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 3809 | chr1 | 92390820 | |||||
chr1:92391250
|
A | G | 2 | a0001c0001t0049a0001c0001t0050 | 2 | HG02257.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4239A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 4239 | chr1 | 92391250 | |||||
chr1:92391334
|
C | T | 1 | a0001c0005t0071 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4323C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 4323 | chr1 | 92391334 | |||||
chr1:92391582
|
G | A | 12 | a0001c0004t0008a0001c0004t0017a0001c0004t0052others(9): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4571G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 4571 | chr1 | 92391582 | |||||
chr1:92391644
|
AAAAAG | A | 6 | a0001c0005t0021a0001c0005t0022a0001c0005t0023others(3): Show | 8 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4636_*4640delAAGA others(1): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 4636 | INFO_REALIGN_3_PRIME | chr1 | 92391644 | ||||
chr1:92391878
|
G | A | 1 | a0001c0001t0049 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4867G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 4867 | chr1 | 92391878 | |||||
chr1:92392001
|
G | A | 1 | a0001c0002t0062 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4990G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 4990 | chr1 | 92392001 | |||||
chr1:92392004
|
G | A | 81 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(78): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*4993G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 4993 | chr1 | 92392004 | |||||
chr1:92392074
|
C | A | 3 | a0002c0013t0011a0002c0013t0068a0002c0048t0011 | 4 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5063C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 5063 | chr1 | 92392074 | |||||
chr1:92392080
|
A | G | 5 | a0002c0013t0011a0002c0013t0068a0002c0047t0069others(2): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5069A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 5069 | chr1 | 92392080 | |||||
chr1:92392088
|
A | G | 5 | a0002c0013t0011a0002c0013t0068a0002c0047t0069others(2): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5077A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 5077 | chr1 | 92392088 | |||||
chr1:92392096
|
G | A | 5 | a0002c0013t0011a0002c0013t0068a0002c0047t0069others(2): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5085G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 5085 | chr1 | 92392096 | |||||
chr1:92392115
|
A | G | 1 | a0001c0038t0048 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5104A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 5104 | chr1 | 92392115 | |||||
chr1:92392118
|
G | A | 5 | a0002c0013t0011a0002c0013t0068a0002c0047t0069others(2): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5107G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 5107 | chr1 | 92392118 | |||||
chr1:92392119
|
A | G | 5 | a0002c0013t0011a0002c0013t0068a0002c0047t0069others(2): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5108A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 5108 | chr1 | 92392119 | |||||
chr1:92392123
|
G | A | 5 | a0002c0013t0011a0002c0013t0068a0002c0047t0069others(2): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5112G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 5112 | chr1 | 92392123 | |||||
chr1:92392145
|
G | A | 45 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(42): Show | 85 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*5134G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 5134 | chr1 | 92392145 | |||||
chr1:92392152
|
G | A | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(41): Show | 84 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*5141G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 5141 | chr1 | 92392152 | |||||
chr1:92392414
|
C | T | 1 | a0001c0002t0065 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5403C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 5403 | chr1 | 92392414 | |||||
chr1:92392640
|
C | T | 3 | a0001c0009t0007a0001c0009t0024a0001c0024t0007 | 5 | HG02258.hp2 HG02723.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5629C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 5629 | chr1 | 92392640 | |||||
chr1:92392683
|
A | G | 1 | a0001c0014t0030 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5672A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 5672 | chr1 | 92392683 | |||||
chr1:92392879
|
C | A | 2 | a0001c0014t0029a0001c0014t0030 | 2 | HG02922.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5868C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 5868 | chr1 | 92392879 | |||||
chr1:92392881
|
A | G | 1 | a0001c0001t0045 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5870A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 5870 | chr1 | 92392881 | |||||
chr1:92393654
|
A | C | 12 | a0001c0004t0008a0001c0004t0017a0001c0004t0052others(9): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*6643A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 6643 | chr1 | 92393654 | |||||
chr1:92393750
|
A | G | 12 | a0001c0004t0008a0001c0004t0017a0001c0004t0052others(9): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*6739A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 6739 | chr1 | 92393750 | |||||
chr1:92394009
|
A | G | 3 | a0001c0004t0008a0001c0004t0053a0001c0025t0008 | 5 | HG02280.hp2 HG06807.hp2 NA19030.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6998A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 6998 | chr1 | 92394009 | |||||
chr1:92394139
|
T | C | 1 | a0001c0044t0057 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7128T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 7128 | chr1 | 92394139 | |||||
chr1:92394192
|
C | T | 1 | a0001c0001t0044 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7181C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 7181 | chr1 | 92394192 | |||||
chr1:92394291
|
A | G | 5 | a0001c0003t0009a0001c0003t0012a0001c0003t0072others(2): Show | 10 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7280A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 7280 | chr1 | 92394291 | |||||
chr1:92394564
|
G | A | 1 | a0001c0007t0031 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7553G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 7553 | chr1 | 92394564 | |||||
chr1:92395405
|
G | A | 2 | a0001c0014t0029a0001c0014t0030 | 2 | HG02922.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8394G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 8394 | chr1 | 92395405 | |||||
chr1:92395598
|
C | T | 26 | a0001c0003t0009a0001c0003t0012a0001c0003t0072others(23): Show | 44 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*8587C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 8587 | chr1 | 92395598 | |||||
chr1:92395605
|
G | C | 1 | a0001c0001t0032 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8594G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 8594 | chr1 | 92395605 | |||||
chr1:92395635
|
CA | C | 27 | a0001c0001t0002a0001c0001t0013a0001c0001t0026others(24): Show | 49 | HG00280.hp1 HG00423.hp1 HG00639.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*8647delA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 8647 | INFO_REALIGN_3_PRIME | chr1 | 92395635 | ||||
chr1:92395635
|
CAA | C | 24 | a0001c0001t0003a0001c0001t0014a0001c0001t0015others(21): Show | 40 | HG00099.hp1 HG01243.hp1 HG01516.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*8646_*8647delAA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 8646 | INFO_REALIGN_3_PRIME | chr1 | 92395635 | ||||
chr1:92395635
|
CAAA | C | 15 | a0001c0004t0008a0001c0004t0017a0001c0004t0067others(12): Show | 31 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*8645_*8647delAAA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 8645 | INFO_REALIGN_3_PRIME | chr1 | 92395635 | ||||
chr1:92395635
|
CAAAA | C | 7 | a0001c0005t0021a0001c0005t0022a0001c0005t0023others(4): Show | 10 | HG01069.hp2 HG01081.hp2 HG01168.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*8644_*8647delAAAA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 8644 | INFO_REALIGN_3_PRIME | chr1 | 92395635 | ||||
chr1:92395750
|
T | C | 25 | a0001c0001t0002a0001c0001t0004a0001c0001t0014others(22): Show | 55 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*8739T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 8739 | chr1 | 92395750 | |||||
chr1:92396060
|
A | G | 1 | a0001c0042t0058 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9049A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 9049 | chr1 | 92396060 | |||||
chr1:92396370
|
C | T | 1 | a0001c0020t0018 | 2 | HG02145.hp2 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9359C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 9359 | chr1 | 92396370 | |||||
chr1:92396476
|
T | C | 1 | a0001c0001t0015 | 2 | HG02622.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9465T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 9465 | chr1 | 92396476 | |||||
chr1:92396489
|
T | C | 47 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(44): Show | 87 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*9478T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 9478 | chr1 | 92396489 | |||||
chr1:92396634
|
A | ATG | 6 | a0001c0005t0023a0001c0014t0029a0001c0014t0030others(3): Show | 7 | HG01891.hp1 HG02622.hp1 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*9646_*9647dupTG | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 9648 | INFO_REALIGN_3_PRIME | chr1 | 92396634 | ||||
chr1:92396634
|
A | ATGTG | 18 | a0001c0001t0003a0001c0001t0013a0001c0001t0015others(15): Show | 28 | HG00099.hp1 HG01243.hp1 HG01516.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*9644_*9647dupTGTG | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 9648 | INFO_REALIGN_3_PRIME | chr1 | 92396634 | ||||
chr1:92396634
|
A | ATGTGTG | 2 | a0001c0001t0042a0001c0001t0043 | 2 | HG02698.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9642_*9647dupTGTG others(2): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 9648 | INFO_REALIGN_3_PRIME | chr1 | 92396634 | ||||
chr1:92396634
|
A | ATGTGTGT others(1): Show |
20 | a0001c0001t0002a0001c0001t0004a0001c0001t0014others(17): Show | 50 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*9640_*9647dupTGTG others(4): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 9648 | INFO_REALIGN_3_PRIME | chr1 | 92396634 | ||||
chr1:92396634
|
A | ATGTGTGT others(3): Show |
5 | a0001c0001t0039a0001c0001t0040a0001c0007t0051others(2): Show | 5 | HG02735.hp2 HG03209.hp1 NA18982.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9638_*9647dupTGTG others(6): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 9648 | INFO_REALIGN_3_PRIME | chr1 | 92396634 | ||||
chr1:92396634
|
ATGTG | A | 1 | a0001c0008t0006 | 6 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9644_*9647delTGTG | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 9644 | INFO_REALIGN_3_PRIME | chr1 | 92396634 | ||||
chr1:92396657
|
TGA | T | 5 | a0002c0013t0011a0002c0013t0068a0002c0047t0069others(2): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9649_*9650delGA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 9649 | INFO_REALIGN_3_PRIME | chr1 | 92396657 | ||||
chr1:92396920
|
G | A | 47 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(44): Show | 87 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*9909G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 9909 | chr1 | 92396920 | |||||
chr1:92397318
|
A | G | 1 | a0001c0001t0037 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10307A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 10307 | chr1 | 92397318 | |||||
chr1:92397349
|
C | T | 12 | a0001c0004t0008a0001c0004t0017a0001c0004t0052others(9): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*10338C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 10338 | chr1 | 92397349 | |||||
chr1:92397546
|
G | A | 47 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(44): Show | 87 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*10535G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 10535 | chr1 | 92397546 | |||||
chr1:92397630
|
G | A | 2 | a0001c0020t0018a0001c0046t0055 | 3 | HG02145.hp2 HG02486.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10619G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 10619 | chr1 | 92397630 | |||||
chr1:92397894
|
C | G | 1 | a0001c0001t0036 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10883C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 10883 | chr1 | 92397894 | |||||
chr1:92397916
|
G | A | 2 | a0001c0005t0022a0001c0021t0022 | 2 | HG01069.hp2 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10905G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 10905 | chr1 | 92397916 | |||||
chr1:92398351
|
C | T | 1 | a0001c0020t0018 | 2 | HG02145.hp2 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11340C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 11340 | chr1 | 92398351 | |||||
chr1:92398409
|
G | A | 3 | a0001c0006t0005a0001c0022t0005a0001c0023t0005 | 8 | HG02630.hp2 HG02647.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*11398G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 11398 | chr1 | 92398409 | |||||
chr1:92398416
|
C | A | 47 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(44): Show | 87 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*11405C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 11405 | chr1 | 92398416 | |||||
chr1:92398520
|
T | C | 1 | a0001c0002t0063 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11509T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 11509 | chr1 | 92398520 | |||||
chr1:92398850
|
A | C | 1 | a0003c0049t0070 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11839A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 11839 | chr1 | 92398850 | |||||
chr1:92399056
|
T | A | 1 | a0001c0002t0060 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12045T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 12045 | chr1 | 92399056 | |||||
chr1:92399188
|
T | G | 1 | a0001c0011t0038 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12177T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 12177 | chr1 | 92399188 | |||||
chr1:92399434
|
G | GAT | 82 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(79): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*12424_*12425insTA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 12425 | INFO_REALIGN_3_PRIME | chr1 | 92399434 | ||||
chr1:92399474
|
C | T | 1 | a0001c0001t0035 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12463C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 12463 | chr1 | 92399474 | |||||
chr1:92399603
|
G | A | 83 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(80): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*12592G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 12592 | chr1 | 92399603 | |||||
chr1:92399617
|
G | T | 26 | a0001c0003t0009a0001c0003t0012a0001c0003t0072others(23): Show | 44 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*12606G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 12606 | chr1 | 92399617 | |||||
chr1:92399956
|
G | A | 2 | a0001c0002t0019a0001c0015t0019 | 2 | HG01069.hp1 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12945G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 12945 | chr1 | 92399956 | |||||
chr1:92400140
|
A | G | 1 | a0001c0001t0044 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13129A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 13129 | chr1 | 92400140 | |||||
chr1:92400261
|
C | T | 1 | a0001c0001t0049 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13250C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 13250 | chr1 | 92400261 | |||||
chr1:92400335
|
G | A | 3 | a0001c0004t0017a0001c0004t0052a0001c0004t0067 | 4 | HG02055.hp1 HG02109.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*13324G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 13324 | chr1 | 92400335 | |||||
chr1:92400398
|
T | G | 14 | a0001c0003t0009a0001c0003t0012a0001c0003t0072others(11): Show | 22 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*13387T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 13387 | chr1 | 92400398 | |||||
chr1:92400877
|
A | G | 12 | a0001c0004t0008a0001c0004t0017a0001c0004t0052others(9): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*13866A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 13866 | chr1 | 92400877 | |||||
chr1:92401035
|
AT | A | 46 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(43): Show | 87 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*14025delT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 14025 | chr1 | 92401035 | |||||
chr1:92401070
|
T | C | 83 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(80): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*14059T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 14059 | chr1 | 92401070 | |||||
chr1:92401149
|
T | C | 2 | a0001c0001t0016a0001c0001t0042 | 3 | HG02258.hp1 HG02698.hp2 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*14138T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 14138 | chr1 | 92401149 | |||||
chr1:92401578
|
T | C | 1 | a0001c0020t0018 | 2 | HG02145.hp2 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*14567T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 14567 | chr1 | 92401578 | |||||
chr1:92401768
|
G | A | 48 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(45): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*14757G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 14757 | chr1 | 92401768 | |||||
chr1:92401948
|
AGGATTTT others(14): Show |
A | 1 | a0001c0036t0041 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14939_*14959delGA others(19): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 14939 | INFO_REALIGN_3_PRIME | chr1 | 92401948 | ||||
chr1:92401977
|
G | C | 1 | a0001c0036t0041 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14966G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 14966 | chr1 | 92401977 | |||||
chr1:92401980
|
T | C | 1 | a0001c0036t0041 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14969T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 14969 | chr1 | 92401980 | |||||
chr1:92401981
|
G | A | 1 | a0001c0036t0041 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14970G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 14970 | chr1 | 92401981 | |||||
chr1:92401982
|
T | G | 1 | a0001c0036t0041 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14971T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 14971 | chr1 | 92401982 | |||||
chr1:92401987
|
T | C | 1 | a0001c0036t0041 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14976T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 14976 | chr1 | 92401987 | |||||
chr1:92401992
|
T | A | 1 | a0001c0036t0041 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14981T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 14981 | chr1 | 92401992 | |||||
chr1:92402000
|
C | A | 1 | a0001c0036t0041 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14989C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 14989 | chr1 | 92402000 | |||||
chr1:92402009
|
G | C | 1 | a0001c0036t0041 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14998G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 14998 | chr1 | 92402009 | |||||
chr1:92402026
|
A | G | 1 | a0001c0036t0041 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*15015A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 13/13 | 15015 | chr1 | 92402026 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:92299201
|
C | G | 2 | a0001c0001t0004g0186a0001c0001t0036g0187 | 2 | HG02135.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.73+55C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 1/12 | chr1 | 92299201 | ||||||
chr1:92299271
|
T | A | 187 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.73+125T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 1/12 | chr1 | 92299271 | ||||||
chr1:92299393
|
C | G | 42 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(39): Show | 44 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.73+247C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 1/12 | chr1 | 92299393 | ||||||
chr1:92299398
|
G | A | 3 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0004g0006 | 3 | HG01943.hp1 HG01978.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.73+252G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 1/12 | chr1 | 92299398 | ||||||
chr1:92299415
|
G | C | 20 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(17): Show | 22 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.73+269G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 1/12 | chr1 | 92299415 | ||||||
chr1:92299545
|
C | T | 86 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(83): Show | 87 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.73+399C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 1/12 | chr1 | 92299545 | ||||||
chr1:92299856
|
AC | A | 3 | a0001c0002t0001g0062a0001c0002t0001g0063a0001c0031t0001g0064 | 3 | HG01123.hp1 HG01361.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.74-336delC | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 92299856 | |||||
chr1:92299946
|
G | A | 1 | a0001c0002t0001g0062 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.74-248G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 1/12 | chr1 | 92299946 | ||||||
chr1:92300142
|
C | T | 1 | a0001c0001t0028g0144 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.74-52C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 1/12 | chr1 | 92300142 | ||||||
chr1:92300291
|
A | T | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.119+52A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 2/12 | chr1 | 92300291 | ||||||
chr1:92300333
|
T | A | 15 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(12): Show | 17 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.119+94T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 2/12 | chr1 | 92300333 | ||||||
chr1:92300334
|
T | G | 15 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(12): Show | 17 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.119+95T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 2/12 | chr1 | 92300334 | ||||||
chr1:92300403
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.119+164C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 2/12 | chr1 | 92300403 | ||||||
chr1:92300508
|
C | G | 4 | a0001c0008t0006g0056a0001c0008t0006g0057a0001c0008t0006g0058others(1): Show | 4 | HG00099.hp2 HG00639.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+269C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 2/12 | chr1 | 92300508 | ||||||
chr1:92300759
|
T | C | 6 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.119+520T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 2/12 | chr1 | 92300759 | ||||||
chr1:92300881
|
G | A | 2 | a0001c0001t0002g0065a0001c0001t0002g0066 | 2 | HG00280.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.120-595G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 2/12 | chr1 | 92300881 | ||||||
chr1:92300909
|
ATTAG | A | 7 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(4): Show | 9 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.120-563_120-560del others(4): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr1 | 92300909 | |||||
chr1:92300923
|
A | C | 1 | a0001c0046t0055g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.120-553A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 2/12 | chr1 | 92300923 | ||||||
chr1:92300945
|
A | T | 1 | a0001c0008t0006g0059 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.120-531A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 2/12 | chr1 | 92300945 | ||||||
chr1:92301205
|
CGGATGTG others(22): Show |
C | 1 | a0001c0007t0004g0067 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.120-269_120-241del others(29): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr1 | 92301205 | |||||
chr1:92301224
|
C | T | 20 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(17): Show | 22 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.120-252C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 2/12 | chr1 | 92301224 | ||||||
chr1:92301291
|
T | C | 130 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(127): Show | 133 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.120-185T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 2/12 | chr1 | 92301291 | ||||||
chr1:92301355
|
T | A | 1 | a0001c0045t0054g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.120-121T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 2/12 | chr1 | 92301355 | ||||||
chr1:92301735
|
A | T | 181 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(178): Show | 185 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.234+145A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | chr1 | 92301735 | ||||||
chr1:92301801
|
C | T | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.234+211C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | chr1 | 92301801 | ||||||
chr1:92301950
|
C | T | 8 | a0001c0006t0005g0178a0001c0006t0005g0179a0001c0006t0005g0180others(5): Show | 8 | HG02630.hp2 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.234+360C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | chr1 | 92301950 | ||||||
chr1:92302128
|
A | G | 1 | a0001c0042t0058g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.234+538A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | chr1 | 92302128 | ||||||
chr1:92302251
|
T | A | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.234+661T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | chr1 | 92302251 | ||||||
chr1:92302254
|
G | A | 1 | a0001c0044t0057g0159 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.234+664G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | chr1 | 92302254 | ||||||
chr1:92302320
|
G | A | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.234+730G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | chr1 | 92302320 | ||||||
chr1:92302330
|
GA | G | 17 | a0001c0002t0063g0055a0001c0003t0009g0001a0001c0003t0009g0147others(14): Show | 19 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.234+753delA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 92302330 | |||||
chr1:92302590
|
A | AT | 30 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0069others(27): Show | 31 | HG00099.hp1 HG01070.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.234+1029dupT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 92302590 | |||||
chr1:92302590
|
A | ATT | 47 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0093others(44): Show | 47 | HG00280.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.234+1028_234+1029d others(4): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 92302590 | |||||
chr1:92302590
|
A | ATTT | 18 | a0001c0001t0002g0131a0001c0001t0002g0133a0001c0001t0002g0137others(15): Show | 18 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.234+1027_234+1029d others(5): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 92302590 | |||||
chr1:92302590
|
A | ATTTT | 5 | a0001c0001t0045g0142a0001c0020t0018g0160a0001c0020t0018g0161others(2): Show | 5 | HG02145.hp2 HG02486.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.234+1026_234+1029d others(6): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 92302590 | |||||
chr1:92302590
|
A | ATTTTTT | 19 | a0001c0002t0001g0002a0001c0002t0001g0019a0001c0002t0001g0020others(16): Show | 20 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.234+1024_234+1029d others(8): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 92302590 | |||||
chr1:92302590
|
A | ATTTTTTT | 15 | a0001c0002t0001g0038a0001c0002t0001g0040a0001c0002t0001g0041others(12): Show | 15 | HG01106.hp2 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.234+1023_234+1029d others(9): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 92302590 | |||||
chr1:92302590
|
A | ATTTTTTT others(1): Show |
7 | a0001c0002t0001g0050a0001c0002t0001g0051a0001c0002t0001g0052others(4): Show | 7 | HG01123.hp1 HG01175.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.234+1022_234+1029d others(10): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 92302590 | |||||
chr1:92302590
|
A | ATTTTTTT others(9): Show |
1 | a0001c0002t0001g0054 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.234+1014_234+1029d others(18): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 92302590 | |||||
chr1:92302590
|
AT | A | 8 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(5): Show | 10 | HG01891.hp2 HG02280.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.234+1029delT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 92302590 | |||||
chr1:92302590
|
ATT | A | 19 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(16): Show | 19 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.234+1028_234+1029d others(4): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 92302590 | |||||
chr1:92303107
|
T | C | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.235-870T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | chr1 | 92303107 | ||||||
chr1:92303186
|
C | G | 1 | a0001c0045t0054g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.235-791C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | chr1 | 92303186 | ||||||
chr1:92303307
|
C | G | 2 | a0001c0019t0013g0126a0001c0019t0034g0088 | 2 | HG02738.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.235-670C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | chr1 | 92303307 | ||||||
chr1:92303567
|
TA | T | 3 | a0001c0020t0018g0160a0001c0020t0018g0161a0001c0046t0055g0162 | 3 | HG02145.hp2 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.235-404delA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 92303567 | |||||
chr1:92303604
|
TTTAG | T | 3 | a0001c0014t0029g0016a0001c0014t0030g0015a0001c0033t0047g0060 | 3 | HG01891.hp1 HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.235-369_235-366del others(4): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 92303604 | |||||
chr1:92303795
|
A | C | 3 | a0001c0020t0018g0160a0001c0020t0018g0161a0001c0046t0055g0162 | 3 | HG02145.hp2 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.235-182A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 3/12 | chr1 | 92303795 | ||||||
chr1:92304172
|
A | G | 1 | a0003c0049t0070g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.333+97A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 4/12 | chr1 | 92304172 | ||||||
chr1:92304202
|
T | C | 8 | a0001c0006t0005g0178a0001c0006t0005g0179a0001c0006t0005g0180others(5): Show | 8 | HG02630.hp2 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-82T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 4/12 | chr1 | 92304202 | ||||||
chr1:92304222
|
G | A | 1 | a0001c0033t0047g0060 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.334-62G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 4/12 | chr1 | 92304222 | ||||||
chr1:92304465
|
T | C | 2 | a0001c0002t0001g0050a0001c0030t0001g0018 | 2 | HG01346.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.399+116T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | chr1 | 92304465 | ||||||
chr1:92304539
|
A | G | 1 | a0001c0014t0029g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.399+190A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | chr1 | 92304539 | ||||||
chr1:92304819
|
A | G | 1 | a0001c0008t0006g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.399+470A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | chr1 | 92304819 | ||||||
chr1:92304862
|
G | A | 42 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(39): Show | 43 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.399+513G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | chr1 | 92304862 | ||||||
chr1:92304906
|
G | A | 9 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.399+557G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | chr1 | 92304906 | ||||||
chr1:92305325
|
C | T | 1 | a0001c0001t0002g0141 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.399+976C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | chr1 | 92305325 | ||||||
chr1:92305432
|
C | CA | 40 | a0001c0001t0002g0143a0001c0002t0001g0002a0001c0002t0001g0017others(37): Show | 41 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.399+1102dupA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAA | 8 | a0001c0001t0002g0120a0001c0001t0043g0084a0001c0002t0001g0038others(5): Show | 8 | HG01168.hp2 HG01169.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.399+1101_399+1102d others(4): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAA | 16 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0077others(13): Show | 17 | HG00099.hp1 HG01081.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.399+1099_399+1102d others(6): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(4): Show |
1 | a0001c0028t0061g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.399+1092_399+1102d others(13): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0013g0073a0001c0018t0003g0118a0001c0040t0002g0119 | 3 | HG03098.hp1 NA18979.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.399+1091_399+1102d others(14): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0003g0072a0001c0001t0015g0138a0001c0001t0015g0139 | 3 | HG01884.hp2 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.399+1090_399+1102d others(15): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0002g0137 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.399+1089_399+1102d others(16): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(8): Show |
5 | a0001c0001t0002g0114a0001c0001t0003g0071a0001c0001t0004g0116others(2): Show | 5 | HG01169.hp2 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+1088_399+1102d others(17): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0002g0113a0001c0001t0004g0136 | 2 | HG01175.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.399+1087_399+1102d others(18): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(10): Show |
3 | a0001c0001t0036g0187a0001c0001t0049g0070a0001c0001t0050g0112 | 3 | HG02135.hp1 HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.399+1086_399+1102d others(19): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0002g0111 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.399+1085_399+1102d others(20): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(15): Show |
4 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(1): Show | 4 | HG02109.hp2 HG02723.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.399+1102_399+1103i others(24): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(16): Show |
1 | a0002c0048t0011g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.399+1102_399+1103i others(25): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(18): Show |
1 | a0001c0016t0020g0135 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.399+1102_399+1103i others(27): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(19): Show |
3 | a0001c0001t0002g0069a0001c0001t0004g0186a0002c0047t0069g0010 | 3 | HG01256.hp2 HG03486.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.399+1102_399+1103i others(28): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(20): Show |
3 | a0001c0001t0002g0108a0001c0001t0014g0110a0001c0001t0035g0109 | 3 | HG01123.hp2 HG01517.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.399+1102_399+1103i others(29): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(21): Show |
11 | a0001c0001t0002g0066a0001c0001t0003g0107a0001c0001t0004g0103others(8): Show | 11 | HG00642.hp1 HG01070.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.399+1102_399+1103i others(30): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(22): Show |
4 | a0001c0001t0002g0141a0001c0007t0051g0099a0001c0041t0004g0100others(1): Show | 4 | HG00642.hp2 HG02080.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.399+1102_399+1103i others(31): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(24): Show |
1 | a0001c0038t0048g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.399+1102_399+1103i others(33): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(25): Show |
2 | a0001c0001t0002g0133a0001c0007t0004g0132 | 2 | HG01106.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.399+1102_399+1103i others(34): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(26): Show |
5 | a0001c0001t0002g0065a0001c0001t0002g0096a0001c0001t0056g0097others(2): Show | 5 | HG00280.hp1 HG00639.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.399+1102_399+1103i others(35): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(27): Show |
6 | a0001c0001t0002g0093a0001c0001t0002g0131a0001c0001t0003g0092others(3): Show | 6 | HG01192.hp2 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.399+1102_399+1103i others(36): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(28): Show |
3 | a0001c0001t0026g0129a0001c0001t0028g0144a0001c0011t0004g0090 | 3 | HG00438.hp2 HG02970.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.399+1102_399+1103i others(37): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(30): Show |
1 | a0001c0034t0002g0128 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.399+1102_399+1103i others(39): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(31): Show |
1 | a0001c0007t0004g0127 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.399+1102_399+1103i others(40): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305432
|
C | CAAAAAAA others(37): Show |
1 | a0001c0011t0003g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.399+1102_399+1103i others(46): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305432 | |||||
chr1:92305450
|
A | AAAAAAAA others(4): Show |
6 | a0001c0004t0008g0163a0001c0004t0017g0164a0001c0004t0017g0165others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.399+1102_399+1103i others(13): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305450 | |||||
chr1:92305450
|
A | AAAAAAAA others(3): Show |
16 | a0001c0004t0008g0168a0001c0004t0008g0169a0001c0004t0053g0167others(13): Show | 16 | HG02258.hp2 HG02280.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.399+1102_399+1103i others(12): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 92305450 | |||||
chr1:92305469
|
T | C | 1 | a0001c0001t0002g0141 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.399+1120T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | chr1 | 92305469 | ||||||
chr1:92305626
|
G | T | 9 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.399+1277G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | chr1 | 92305626 | ||||||
chr1:92305627
|
A | T | 9 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.399+1278A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | chr1 | 92305627 | ||||||
chr1:92305780
|
A | G | 1 | a0001c0033t0047g0060 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.400-1408A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | chr1 | 92305780 | ||||||
chr1:92305959
|
C | T | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.400-1229C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | chr1 | 92305959 | ||||||
chr1:92306528
|
A | C | 2 | a0001c0001t0015g0138a0001c0001t0015g0139 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.400-660A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | chr1 | 92306528 | ||||||
chr1:92306785
|
G | A | 43 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(40): Show | 44 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.400-403G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | chr1 | 92306785 | ||||||
chr1:92306914
|
A | G | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.400-274A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | chr1 | 92306914 | ||||||
chr1:92306945
|
G | A | 1 | a0001c0001t0003g0003 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.400-243G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 5/12 | chr1 | 92306945 | ||||||
chr1:92307507
|
A | G | 1 | a0001c0001t0002g0113 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.488+231A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92307507 | ||||||
chr1:92307726
|
A | AT | 136 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(133): Show | 139 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.488+461dupT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 92307726 | |||||
chr1:92307726
|
A | ATT | 44 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(41): Show | 45 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.488+460_488+461dup others(2): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 92307726 | |||||
chr1:92307957
|
G | T | 1 | a0001c0033t0047g0060 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.488+681G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92307957 | ||||||
chr1:92308003
|
T | A | 1 | a0001c0033t0047g0060 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.488+727T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92308003 | ||||||
chr1:92308013
|
C | T | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.488+737C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92308013 | ||||||
chr1:92308156
|
A | G | 7 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(4): Show | 9 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.488+880A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92308156 | ||||||
chr1:92308441
|
C | T | 2 | a0001c0020t0018g0160a0001c0020t0018g0161 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.488+1165C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92308441 | ||||||
chr1:92308829
|
G | A | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.488+1553G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92308829 | ||||||
chr1:92309210
|
G | A | 42 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(39): Show | 43 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.488+1934G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92309210 | ||||||
chr1:92309352
|
G | C | 2 | a0001c0001t0015g0138a0001c0001t0015g0139 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.488+2076G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92309352 | ||||||
chr1:92309396
|
C | T | 1 | a0001c0042t0058g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.488+2120C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92309396 | ||||||
chr1:92309440
|
C | CA | 93 | a0001c0001t0002g0069a0001c0002t0001g0002a0001c0002t0001g0017others(90): Show | 96 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(93): Show |
intron_variant | MODIFIER | c.488+2177dupA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 92309440 | |||||
chr1:92309440
|
C | CAA | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.488+2176_488+2177d others(4): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 92309440 | |||||
chr1:92309536
|
CACACAT | C | 14 | a0001c0001t0002g0114a0001c0001t0002g0120a0001c0001t0032g0091others(11): Show | 14 | HG01123.hp1 HG01175.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.488+2292_488+2297d others(8): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 92309536 | |||||
chr1:92309536
|
CACACATA others(5): Show |
C | 1 | a0001c0002t0001g0017 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.488+2286_488+2297d others(14): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 92309536 | |||||
chr1:92309544
|
CACATACA others(29): Show |
C | 4 | a0001c0004t0017g0164a0001c0004t0017g0165a0001c0004t0052g0166others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.488+2298_488+2333d others(38): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 92309544 | |||||
chr1:92309550
|
CACATACA others(23): Show |
C | 9 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(6): Show | 11 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.488+2298_488+2327d others(32): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 92309550 | |||||
chr1:92309556
|
CACATACA others(11): Show |
C | 1 | a0001c0046t0055g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.488+2286_488+2303d others(20): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 92309556 | |||||
chr1:92309556
|
CACATACA others(17): Show |
C | 10 | a0001c0005t0021g0153a0001c0005t0021g0154a0001c0005t0022g0150others(7): Show | 10 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.488+2298_488+2321d others(26): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 92309556 | |||||
chr1:92309562
|
CACATACA others(5): Show |
C | 119 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(116): Show | 121 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.488+2292_488+2303d others(14): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 92309562 | |||||
chr1:92309568
|
C | T | 23 | a0001c0001t0004g0186a0001c0001t0015g0139a0001c0002t0001g0034others(20): Show | 23 | HG01070.hp1 HG01891.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.488+2292C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92309568 | ||||||
chr1:92309574
|
TACATATA others(11): Show |
T | 5 | a0001c0001t0004g0186a0001c0001t0015g0139a0001c0002t0001g0034others(2): Show | 5 | HG01070.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.488+2304_488+2321d others(20): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 92309574 | |||||
chr1:92309574
|
TACATATA others(17): Show |
T | 18 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(15): Show | 18 | HG02258.hp2 HG02280.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.488+2304_488+2327d others(26): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 92309574 | |||||
chr1:92309586
|
C | T | 130 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.488+2310C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92309586 | ||||||
chr1:92309592
|
C | T | 19 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(16): Show | 21 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.488+2316C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92309592 | ||||||
chr1:92309598
|
C | T | 13 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(10): Show | 15 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.488+2322C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92309598 | ||||||
chr1:92309604
|
C | T | 4 | a0001c0004t0017g0164a0001c0004t0017g0165a0001c0004t0052g0166others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.488+2328C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92309604 | ||||||
chr1:92309899
|
T | C | 1 | a0001c0006t0005g0184 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.488+2623T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92309899 | ||||||
chr1:92310156
|
T | C | 1 | a0001c0042t0058g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.488+2880T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92310156 | ||||||
chr1:92310181
|
G | A | 4 | a0001c0004t0017g0164a0001c0004t0017g0165a0001c0004t0052g0166others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.488+2905G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92310181 | ||||||
chr1:92310182
|
T | A | 1 | a0001c0018t0003g0085 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.488+2906T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92310182 | ||||||
chr1:92310384
|
G | A | 8 | a0001c0006t0005g0178a0001c0006t0005g0179a0001c0006t0005g0180others(5): Show | 8 | HG02630.hp2 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.488+3108G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92310384 | ||||||
chr1:92310788
|
T | G | 18 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(15): Show | 18 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.488+3512T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92310788 | ||||||
chr1:92310955
|
A | G | 1 | a0001c0001t0032g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.488+3679A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92310955 | ||||||
chr1:92311145
|
G | A | 2 | a0001c0001t0004g0136a0001c0001t0037g0115 | 2 | HG01169.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.488+3869G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92311145 | ||||||
chr1:92311148
|
T | A | 1 | a0001c0002t0001g0052 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.488+3872T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92311148 | ||||||
chr1:92311637
|
T | C | 1 | a0001c0017t0002g0101 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.488+4361T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92311637 | ||||||
chr1:92311962
|
G | A | 1 | a0001c0006t0005g0178 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.488+4686G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92311962 | ||||||
chr1:92312044
|
C | G | 1 | a0001c0024t0007g0176 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.488+4768C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92312044 | ||||||
chr1:92312171
|
C | T | 24 | a0001c0001t0002g0125a0001c0001t0002g0131a0001c0001t0014g0110others(21): Show | 26 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.488+4895C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92312171 | ||||||
chr1:92312331
|
G | T | 1 | a0001c0002t0001g0048 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.488+5055G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92312331 | ||||||
chr1:92312412
|
G | A | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.488+5136G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92312412 | ||||||
chr1:92312418
|
CA | C | 155 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0066others(152): Show | 159 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.488+5157delA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 92312418 | |||||
chr1:92312600
|
C | T | 1 | a0001c0010t0002g0083 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.488+5324C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92312600 | ||||||
chr1:92312743
|
C | T | 1 | a0001c0046t0055g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.488+5467C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92312743 | ||||||
chr1:92313051
|
A | G | 1 | a0001c0002t0001g0053 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.488+5775A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92313051 | ||||||
chr1:92313341
|
T | C | 2 | a0001c0005t0022g0150a0001c0021t0022g0151 | 2 | HG01069.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.488+6065T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92313341 | ||||||
chr1:92313443
|
C | CT | 127 | a0001c0001t0002g0005a0001c0001t0002g0065a0001c0001t0002g0066others(124): Show | 129 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.488+6181dupT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 92313443 | |||||
chr1:92313735
|
G | A | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.488+6459G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92313735 | ||||||
chr1:92314012
|
G | A | 1 | a0001c0001t0003g0003 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.489-6587G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92314012 | ||||||
chr1:92314062
|
T | A | 2 | a0001c0018t0003g0085a0001c0018t0003g0118 | 2 | NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.489-6537T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92314062 | ||||||
chr1:92314306
|
G | T | 7 | a0001c0005t0021g0153a0001c0005t0021g0154a0001c0005t0022g0150others(4): Show | 7 | HG01069.hp2 HG01081.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.489-6293G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92314306 | ||||||
chr1:92314348
|
T | G | 2 | a0001c0044t0057g0159a0001c0045t0054g0158 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.489-6251T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92314348 | ||||||
chr1:92314351
|
G | GT | 45 | a0001c0001t0003g0107a0001c0001t0044g0082a0001c0003t0009g0001others(42): Show | 47 | HG00099.hp1 HG01069.hp2 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.489-6235dupT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 92314351 | |||||
chr1:92314400
|
A | T | 3 | a0001c0005t0021g0153a0001c0005t0021g0154a0001c0005t0071g0157 | 3 | HG01081.hp2 HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.489-6199A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92314400 | ||||||
chr1:92314528
|
T | G | 26 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(23): Show | 27 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.489-6071T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92314528 | ||||||
chr1:92314749
|
T | C | 1 | a0001c0001t0027g0122 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.489-5850T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92314749 | ||||||
chr1:92314821
|
G | T | 3 | a0001c0020t0018g0160a0001c0020t0018g0161a0001c0046t0055g0162 | 3 | HG02145.hp2 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.489-5778G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92314821 | ||||||
chr1:92314901
|
C | T | 9 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.489-5698C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92314901 | ||||||
chr1:92314949
|
G | A | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.489-5650G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92314949 | ||||||
chr1:92315580
|
T | A | 1 | a0001c0036t0041g0095 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.489-5019T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92315580 | ||||||
chr1:92316002
|
C | T | 40 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(37): Show | 42 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.489-4597C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92316002 | ||||||
chr1:92316022
|
C | T | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.489-4577C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92316022 | ||||||
chr1:92316059
|
C | T | 2 | a0001c0020t0018g0160a0001c0020t0018g0161 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.489-4540C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92316059 | ||||||
chr1:92316325
|
G | C | 1 | a0001c0001t0002g0113 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.489-4274G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92316325 | ||||||
chr1:92316610
|
A | G | 1 | a0001c0044t0057g0159 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.489-3989A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92316610 | ||||||
chr1:92316793
|
G | A | 1 | a0001c0002t0001g0028 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.489-3806G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92316793 | ||||||
chr1:92317133
|
A | T | 1 | a0001c0030t0001g0018 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.489-3466A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92317133 | ||||||
chr1:92317323
|
A | G | 9 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.489-3276A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92317323 | ||||||
chr1:92317637
|
C | T | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.489-2962C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92317637 | ||||||
chr1:92317679
|
A | C | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.489-2920A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92317679 | ||||||
chr1:92317765
|
C | T | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.489-2834C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92317765 | ||||||
chr1:92317809
|
A | C | 20 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(17): Show | 22 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.489-2790A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92317809 | ||||||
chr1:92318244
|
A | G | 1 | a0001c0041t0004g0100 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.489-2355A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92318244 | ||||||
chr1:92318587
|
C | T | 7 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(4): Show | 9 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.489-2012C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92318587 | ||||||
chr1:92318755
|
T | C | 3 | a0001c0020t0018g0160a0001c0020t0018g0161a0001c0046t0055g0162 | 3 | HG02145.hp2 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.489-1844T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92318755 | ||||||
chr1:92318975
|
A | G | 1 | a0001c0005t0073g0155 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.489-1624A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92318975 | ||||||
chr1:92319336
|
T | C | 4 | a0001c0009t0007g0172a0001c0009t0007g0173a0001c0009t0007g0175others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.489-1263T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92319336 | ||||||
chr1:92319492
|
G | A | 1 | a0001c0005t0073g0155 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.489-1107G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92319492 | ||||||
chr1:92319923
|
G | A | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.489-676G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92319923 | ||||||
chr1:92320158
|
CTT | C | 3 | a0001c0009t0007g0172a0001c0009t0007g0173a0001c0009t0024g0174 | 3 | HG02258.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.489-439_489-438del others(2): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 92320158 | |||||
chr1:92320188
|
C | T | 15 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(12): Show | 17 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.489-411C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92320188 | ||||||
chr1:92320387
|
C | T | 2 | a0001c0020t0018g0160a0001c0020t0018g0161 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.489-212C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92320387 | ||||||
chr1:92320425
|
G | A | 5 | a0001c0001t0003g0092a0001c0001t0003g0107a0001c0001t0028g0144others(2): Show | 5 | HG02818.hp2 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.489-174G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 6/12 | chr1 | 92320425 | ||||||
chr1:92321004
|
G | C | 1 | a0001c0001t0036g0187 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.524+370G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | chr1 | 92321004 | ||||||
chr1:92321122
|
TC | T | 20 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(17): Show | 22 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.524+491delC | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 92321122 | |||||
chr1:92321180
|
G | A | 1 | a0001c0045t0054g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.524+546G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | chr1 | 92321180 | ||||||
chr1:92321185
|
G | T | 51 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(48): Show | 52 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.524+551G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | chr1 | 92321185 | ||||||
chr1:92321476
|
A | T | 15 | a0001c0009t0007g0172a0001c0009t0007g0173a0001c0009t0007g0175others(12): Show | 15 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.524+842A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | chr1 | 92321476 | ||||||
chr1:92321596
|
T | C | 8 | a0001c0006t0005g0178a0001c0006t0005g0179a0001c0006t0005g0180others(5): Show | 8 | HG02630.hp2 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.524+962T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | chr1 | 92321596 | ||||||
chr1:92321610
|
G | A | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.524+976G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | chr1 | 92321610 | ||||||
chr1:92321820
|
A | G | 1 | a0001c0017t0002g0068 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.524+1186A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | chr1 | 92321820 | ||||||
chr1:92321971
|
A | T | 1 | a0001c0042t0058g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.524+1337A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | chr1 | 92321971 | ||||||
chr1:92322091
|
A | T | 1 | a0001c0001t0002g0066 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.525-1354A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | chr1 | 92322091 | ||||||
chr1:92322197
|
T | C | 3 | a0001c0001t0016g0075a0001c0001t0016g0086a0001c0001t0042g0074 | 3 | HG02258.hp1 HG02698.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.525-1248T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | chr1 | 92322197 | ||||||
chr1:92322243
|
G | T | 9 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.525-1202G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | chr1 | 92322243 | ||||||
chr1:92322244
|
C | T | 9 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.525-1201C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | chr1 | 92322244 | ||||||
chr1:92322508
|
C | T | 1 | a0001c0001t0045g0142 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.525-937C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | chr1 | 92322508 | ||||||
chr1:92322575
|
A | G | 1 | a0001c0042t0058g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.525-870A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | chr1 | 92322575 | ||||||
chr1:92322597
|
G | A | 6 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.525-848G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | chr1 | 92322597 | ||||||
chr1:92322799
|
C | A | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.525-646C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | chr1 | 92322799 | ||||||
chr1:92322860
|
C | CAGTG | 187 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.525-583_525-582ins others(4): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 92322860 | |||||
chr1:92322914
|
AT | A | 20 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(17): Show | 22 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.525-525delT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 92322914 | |||||
chr1:92323034
|
TTA | T | 2 | a0002c0047t0069g0010a0003c0049t0070g0009 | 2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.525-405_525-404del others(2): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 92323034 | |||||
chr1:92323087
|
A | T | 42 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(39): Show | 43 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.525-358A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | chr1 | 92323087 | ||||||
chr1:92323147
|
T | A | 5 | a0001c0005t0021g0153a0001c0005t0021g0154a0001c0005t0071g0157others(2): Show | 5 | HG01081.hp2 HG01884.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.525-298T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | chr1 | 92323147 | ||||||
chr1:92323212
|
T | G | 181 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(178): Show | 185 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.525-233T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 7/12 | chr1 | 92323212 | ||||||
chr1:92324938
|
T | A | 6 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1455+563T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92324938 | ||||||
chr1:92325160
|
T | C | 2 | a0001c0001t0004g0136a0001c0001t0037g0115 | 2 | HG01169.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1455+785T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92325160 | ||||||
chr1:92325195
|
C | T | 2 | a0001c0001t0014g0110a0001c0001t0039g0087 | 2 | HG01517.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1455+820C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92325195 | ||||||
chr1:92325926
|
T | G | 7 | a0001c0005t0021g0153a0001c0005t0021g0154a0001c0005t0022g0150others(4): Show | 7 | HG01069.hp2 HG01081.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1455+1551T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92325926 | ||||||
chr1:92325969
|
A | G | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1455+1594A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92325969 | ||||||
chr1:92326066
|
C | T | 6 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1455+1691C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92326066 | ||||||
chr1:92326255
|
G | T | 181 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(178): Show | 185 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1455+1880G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92326255 | ||||||
chr1:92326513
|
C | G | 1 | a0001c0045t0054g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1455+2138C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92326513 | ||||||
chr1:92326598
|
G | A | 2 | a0001c0001t0015g0138a0001c0001t0015g0139 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1455+2223G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92326598 | ||||||
chr1:92326710
|
G | A | 1 | a0001c0042t0058g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1455+2335G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92326710 | ||||||
chr1:92326805
|
C | A | 1 | a0001c0045t0054g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1455+2430C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92326805 | ||||||
chr1:92326918
|
C | T | 15 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(12): Show | 17 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1455+2543C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92326918 | ||||||
chr1:92327174
|
T | A | 2 | a0001c0005t0022g0150a0001c0021t0022g0151 | 2 | HG01069.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.1455+2799T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92327174 | ||||||
chr1:92327233
|
C | T | 1 | a0001c0005t0073g0155 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1455+2858C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92327233 | ||||||
chr1:92327301
|
C | T | 181 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(178): Show | 185 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1455+2926C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92327301 | ||||||
chr1:92327373
|
T | C | 43 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(40): Show | 44 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.1455+2998T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92327373 | ||||||
chr1:92327481
|
C | T | 5 | a0001c0009t0007g0172a0001c0009t0007g0173a0001c0009t0007g0175others(2): Show | 5 | HG02258.hp2 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1455+3106C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92327481 | ||||||
chr1:92327485
|
C | T | 1 | a0001c0001t0043g0084 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1455+3110C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92327485 | ||||||
chr1:92327497
|
A | G | 1 | a0001c0025t0008g0170 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1455+3122A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92327497 | ||||||
chr1:92327585
|
G | C | 1 | a0001c0034t0002g0128 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1455+3210G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92327585 | ||||||
chr1:92327715
|
C | CT | 40 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(37): Show | 42 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1455+3351dupT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 92327715 | |||||
chr1:92327774
|
G | T | 1 | a0003c0049t0070g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1455+3399G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92327774 | ||||||
chr1:92327923
|
C | T | 3 | a0001c0005t0021g0153a0001c0005t0021g0154a0001c0005t0071g0157 | 3 | HG01081.hp2 HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1455+3548C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92327923 | ||||||
chr1:92327986
|
A | G | 1 | a0001c0002t0063g0055 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1455+3611A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92327986 | ||||||
chr1:92328109
|
C | T | 1 | a0002c0047t0069g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1455+3734C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92328109 | ||||||
chr1:92328138
|
A | G | 1 | a0001c0044t0057g0159 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1455+3763A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92328138 | ||||||
chr1:92328293
|
ATTCTTAG others(27): Show |
A | 1 | a0001c0016t0020g0135 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1455+3924_1455+395 others(38): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 92328293 | |||||
chr1:92328370
|
T | C | 1 | a0001c0028t0061g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1455+3995T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92328370 | ||||||
chr1:92328386
|
CAA | C | 3 | a0001c0009t0007g0172a0001c0009t0007g0173a0001c0009t0024g0174 | 3 | HG02258.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1455+4014_1455+401 others(6): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 92328386 | |||||
chr1:92328474
|
T | C | 43 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(40): Show | 44 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.1455+4099T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92328474 | ||||||
chr1:92328944
|
C | T | 3 | a0001c0009t0007g0172a0001c0009t0007g0173a0001c0009t0024g0174 | 3 | HG02258.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1456-4447C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92328944 | ||||||
chr1:92328955
|
C | T | 7 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(4): Show | 9 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1456-4436C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92328955 | ||||||
chr1:92329033
|
G | A | 48 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0069others(45): Show | 48 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1456-4358G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92329033 | ||||||
chr1:92329201
|
T | C | 181 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(178): Show | 185 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1456-4190T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92329201 | ||||||
chr1:92329547
|
C | T | 6 | a0001c0008t0006g0013a0001c0008t0006g0014a0001c0008t0006g0056others(3): Show | 6 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(3): Show |
intron_variant | MODIFIER | c.1456-3844C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92329547 | ||||||
chr1:92329623
|
T | A | 3 | a0001c0002t0001g0048a0001c0002t0062g0045a0004c0026t0001g0029 | 3 | HG01256.hp1 HG01981.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1456-3768T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92329623 | ||||||
chr1:92329631
|
T | C | 3 | a0001c0009t0007g0172a0001c0009t0007g0173a0001c0009t0024g0174 | 3 | HG02258.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1456-3760T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92329631 | ||||||
chr1:92329794
|
C | T | 1 | a0001c0002t0001g0020 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1456-3597C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92329794 | ||||||
chr1:92329840
|
C | T | 1 | a0001c0044t0057g0159 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1456-3551C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92329840 | ||||||
chr1:92329935
|
C | T | 5 | a0001c0001t0003g0092a0001c0001t0003g0107a0001c0001t0028g0144others(2): Show | 5 | HG02818.hp2 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1456-3456C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92329935 | ||||||
chr1:92329940
|
A | C | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1456-3451A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92329940 | ||||||
chr1:92330007
|
C | A | 6 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1456-3384C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92330007 | ||||||
chr1:92330104
|
C | T | 3 | a0001c0020t0018g0160a0001c0020t0018g0161a0001c0046t0055g0162 | 3 | HG02145.hp2 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1456-3287C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92330104 | ||||||
chr1:92330282
|
G | A | 1 | a0001c0005t0021g0153 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1456-3109G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92330282 | ||||||
chr1:92330439
|
A | AT | 43 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(40): Show | 44 | HG00099.hp2 HG00438.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.1456-2925dupT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 92330439 | |||||
chr1:92330439
|
A | ATT | 11 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0004t0008g0169others(8): Show | 11 | HG00741.hp2 HG01175.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1456-2926_1456-292 others(6): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 92330439 | |||||
chr1:92330439
|
AT | A | 68 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(65): Show | 69 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.1456-2925delT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 92330439 | |||||
chr1:92330439
|
ATT | A | 5 | a0001c0001t0037g0115a0001c0005t0021g0154a0001c0044t0057g0159others(2): Show | 5 | HG01169.hp2 HG02630.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1456-2926_1456-292 others(6): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 92330439 | |||||
chr1:92330482
|
C | G | 4 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0053g0167others(1): Show | 4 | HG02280.hp2 HG06807.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1456-2909C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92330482 | ||||||
chr1:92330550
|
C | T | 1 | a0001c0006t0005g0183 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1456-2841C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92330550 | ||||||
chr1:92331026
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1456-2365C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92331026 | ||||||
chr1:92331191
|
A | G | 8 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(5): Show | 10 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1456-2200A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92331191 | ||||||
chr1:92331474
|
A | T | 1 | a0001c0037t0003g0140 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1456-1917A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92331474 | ||||||
chr1:92331536
|
C | A | 6 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1456-1855C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92331536 | ||||||
chr1:92332022
|
C | A | 2 | a0001c0002t0001g0019a0001c0002t0001g0022 | 2 | HG01257.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1456-1369C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92332022 | ||||||
chr1:92332149
|
C | T | 1 | a0001c0044t0057g0159 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1456-1242C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92332149 | ||||||
chr1:92332219
|
A | T | 1 | a0001c0030t0001g0018 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1456-1172A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92332219 | ||||||
chr1:92332257
|
C | A | 181 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(178): Show | 185 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1456-1134C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92332257 | ||||||
chr1:92332323
|
G | A | 3 | a0001c0020t0018g0160a0001c0020t0018g0161a0001c0046t0055g0162 | 3 | HG02145.hp2 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1456-1068G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92332323 | ||||||
chr1:92332434
|
T | C | 8 | a0001c0006t0005g0178a0001c0006t0005g0179a0001c0006t0005g0180others(5): Show | 8 | HG02630.hp2 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1456-957T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92332434 | ||||||
chr1:92332474
|
G | T | 181 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(178): Show | 185 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1456-917G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92332474 | ||||||
chr1:92333106
|
C | A | 1 | a0001c0011t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1456-285C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92333106 | ||||||
chr1:92333356
|
G | C | 1 | a0001c0045t0054g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1456-35G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92333356 | ||||||
chr1:92333388
|
C | T | 1 | a0001c0001t0002g0141 | 1 | HG02080.hp1 | splice_region_variant&intron_variant | LOW | c.1456-3C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 8/12 | chr1 | 92333388 | ||||||
chr1:92333594
|
C | T | 181 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(178): Show | 185 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1538+121C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 9/12 | chr1 | 92333594 | ||||||
chr1:92333608
|
C | T | 2 | a0001c0005t0023g0152a0001c0005t0023g0156 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1538+135C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 9/12 | chr1 | 92333608 | ||||||
chr1:92334350
|
T | C | 1 | a0001c0008t0006g0013 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1538+877T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 9/12 | chr1 | 92334350 | ||||||
chr1:92334675
|
A | C | 181 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(178): Show | 185 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1538+1202A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 9/12 | chr1 | 92334675 | ||||||
chr1:92334708
|
C | T | 43 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(40): Show | 44 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.1538+1235C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 9/12 | chr1 | 92334708 | ||||||
chr1:92334810
|
C | T | 2 | a0001c0008t0006g0057a0001c0008t0006g0058 | 2 | HG00099.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.1538+1337C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 9/12 | chr1 | 92334810 | ||||||
chr1:92334919
|
C | T | 1 | a0001c0005t0073g0155 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1539-1428C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 9/12 | chr1 | 92334919 | ||||||
chr1:92335089
|
G | T | 1 | a0001c0005t0073g0155 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1539-1258G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 9/12 | chr1 | 92335089 | ||||||
chr1:92335314
|
C | T | 187 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1539-1033C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 9/12 | chr1 | 92335314 | ||||||
chr1:92335653
|
A | C | 1 | a0001c0007t0031g0105 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1539-694A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 9/12 | chr1 | 92335653 | ||||||
chr1:92335752
|
A | G | 15 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(12): Show | 17 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1539-595A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 9/12 | chr1 | 92335752 | ||||||
chr1:92336073
|
TA | T | 6 | a0001c0002t0001g0021a0001c0002t0001g0028a0001c0002t0001g0032others(3): Show | 6 | HG01106.hp2 HG03710.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539-272delA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 92336073 | |||||
chr1:92336305
|
T | A | 1 | a0001c0046t0055g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1539-42T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 9/12 | chr1 | 92336305 | ||||||
chr1:92336444
|
C | T | 5 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(2): Show | 5 | HG02280.hp2 HG06807.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1619+17C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92336444 | ||||||
chr1:92336504
|
A | C | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1619+77A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92336504 | ||||||
chr1:92336528
|
A | G | 2 | a0001c0020t0018g0160a0001c0020t0018g0161 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1619+101A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92336528 | ||||||
chr1:92336593
|
A | G | 1 | a0001c0001t0002g0065 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1619+166A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92336593 | ||||||
chr1:92336654
|
G | A | 1 | a0001c0008t0006g0057 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1619+227G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92336654 | ||||||
chr1:92336829
|
ATG | A | 7 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(4): Show | 9 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1619+405_1619+406d others(4): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 92336829 | |||||
chr1:92337161
|
C | A | 1 | a0001c0002t0001g0052 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1619+734C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92337161 | ||||||
chr1:92337202
|
A | G | 42 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(39): Show | 44 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.1619+775A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92337202 | ||||||
chr1:92337270
|
C | G | 1 | a0001c0001t0040g0104 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1619+843C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92337270 | ||||||
chr1:92337426
|
G | A | 42 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(39): Show | 44 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.1619+999G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92337426 | ||||||
chr1:92337798
|
G | A | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1619+1371G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92337798 | ||||||
chr1:92337995
|
A | G | 1 | a0001c0032t0033g0134 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1619+1568A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92337995 | ||||||
chr1:92338262
|
A | G | 9 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1619+1835A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92338262 | ||||||
chr1:92338293
|
C | G | 1 | a0001c0033t0047g0060 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1619+1866C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92338293 | ||||||
chr1:92338412
|
A | C | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1619+1985A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92338412 | ||||||
chr1:92338648
|
A | AT | 89 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(86): Show | 90 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.1619+2240dupT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 92338648 | |||||
chr1:92338648
|
AT | A | 62 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(59): Show | 65 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(62): Show |
intron_variant | MODIFIER | c.1619+2240delT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 92338648 | |||||
chr1:92338682
|
G | T | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1619+2255G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92338682 | ||||||
chr1:92338683
|
C | T | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1619+2256C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92338683 | ||||||
chr1:92338685
|
C | T | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1619+2258C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92338685 | ||||||
chr1:92338686
|
A | T | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1619+2259A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92338686 | ||||||
chr1:92338687
|
G | T | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1619+2260G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92338687 | ||||||
chr1:92338688
|
T | TA | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1619+2261_1619+226 others(5): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92338688 | ||||||
chr1:92338689
|
T | A | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1619+2262T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92338689 | ||||||
chr1:92338690
|
G | A | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1619+2263G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92338690 | ||||||
chr1:92338691
|
C | G | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1619+2264C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92338691 | ||||||
chr1:92338692
|
C | A | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1619+2265C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92338692 | ||||||
chr1:92338801
|
A | G | 2 | a0001c0044t0057g0159a0001c0045t0054g0158 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1619+2374A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92338801 | ||||||
chr1:92339032
|
A | G | 20 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0077others(17): Show | 21 | HG00099.hp1 HG01081.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1619+2605A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92339032 | ||||||
chr1:92339092
|
A | G | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1619+2665A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92339092 | ||||||
chr1:92339320
|
G | A | 1 | a0001c0020t0018g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1619+2893G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92339320 | ||||||
chr1:92339332
|
G | A | 1 | a0001c0002t0065g0023 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1619+2905G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92339332 | ||||||
chr1:92339332
|
G | GC | 15 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(12): Show | 17 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1619+2911dupC | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 92339332 | |||||
chr1:92339665
|
C | T | 51 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(48): Show | 52 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.1619+3238C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92339665 | ||||||
chr1:92339666
|
G | A | 3 | a0001c0009t0007g0172a0001c0009t0007g0173a0001c0009t0024g0174 | 3 | HG02258.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1619+3239G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92339666 | ||||||
chr1:92339905
|
A | G | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1619+3478A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92339905 | ||||||
chr1:92340251
|
A | G | 1 | a0001c0001t0003g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1619+3824A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92340251 | ||||||
chr1:92340824
|
G | A | 7 | a0001c0005t0021g0153a0001c0005t0021g0154a0001c0005t0022g0150others(4): Show | 7 | HG01069.hp2 HG01081.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1619+4397G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92340824 | ||||||
chr1:92341102
|
A | G | 130 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(127): Show | 133 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.1619+4675A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92341102 | ||||||
chr1:92341390
|
T | C | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1620-4456T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92341390 | ||||||
chr1:92341537
|
G | A | 1 | a0001c0001t0026g0129 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1620-4309G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92341537 | ||||||
chr1:92341681
|
G | A | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1620-4165G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92341681 | ||||||
chr1:92341693
|
G | A | 9 | a0001c0001t0036g0187a0001c0007t0004g0102a0001c0007t0004g0127others(6): Show | 9 | HG00642.hp2 HG01106.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.1620-4153G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92341693 | ||||||
chr1:92341780
|
G | A | 3 | a0001c0020t0018g0160a0001c0020t0018g0161a0001c0046t0055g0162 | 3 | HG02145.hp2 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1620-4066G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92341780 | ||||||
chr1:92341906
|
G | A | 2 | a0001c0044t0057g0159a0001c0045t0054g0158 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1620-3940G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92341906 | ||||||
chr1:92342119
|
A | G | 1 | a0001c0005t0071g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1620-3727A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92342119 | ||||||
chr1:92342191
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1620-3655G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92342191 | ||||||
chr1:92342396
|
G | T | 2 | a0001c0012t0010g0037a0001c0012t0010g0039 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1620-3450G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92342396 | ||||||
chr1:92342409
|
A | G | 1 | a0001c0045t0054g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1620-3437A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92342409 | ||||||
chr1:92342570
|
T | C | 6 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1620-3276T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92342570 | ||||||
chr1:92342579
|
G | C | 1 | a0002c0047t0069g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1620-3267G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92342579 | ||||||
chr1:92342748
|
C | A | 4 | a0001c0001t0002g0114a0001c0001t0002g0120a0001c0017t0002g0101others(1): Show | 4 | HG02809.hp2 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1620-3098C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92342748 | ||||||
chr1:92342777
|
T | C | 57 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(54): Show | 57 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.1620-3069T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92342777 | ||||||
chr1:92342930
|
C | T | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1620-2916C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92342930 | ||||||
chr1:92343144
|
G | A | 8 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(5): Show | 10 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1620-2702G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92343144 | ||||||
chr1:92343263
|
G | A | 3 | a0001c0020t0018g0160a0001c0020t0018g0161a0001c0046t0055g0162 | 3 | HG02145.hp2 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1620-2583G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92343263 | ||||||
chr1:92343433
|
C | A | 6 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1620-2413C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92343433 | ||||||
chr1:92343515
|
A | C | 15 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(12): Show | 17 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1620-2331A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92343515 | ||||||
chr1:92343698
|
A | G | 1 | a0001c0002t0001g0044 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1620-2148A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92343698 | ||||||
chr1:92343737
|
AATTATAT | A | 45 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(42): Show | 46 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.1620-2104_1620-209 others(11): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 92343737 | |||||
chr1:92343832
|
G | A | 1 | a0001c0044t0057g0159 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1620-2014G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92343832 | ||||||
chr1:92343840
|
T | C | 1 | a0002c0013t0068g0008 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1620-2006T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92343840 | ||||||
chr1:92343872
|
A | G | 1 | a0001c0002t0001g0053 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1620-1974A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92343872 | ||||||
chr1:92344041
|
C | T | 1 | a0001c0044t0057g0159 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1620-1805C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92344041 | ||||||
chr1:92344265
|
C | T | 6 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1620-1581C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92344265 | ||||||
chr1:92344356
|
G | C | 1 | a0001c0002t0001g0021 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1620-1490G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92344356 | ||||||
chr1:92344658
|
C | A | 9 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1620-1188C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92344658 | ||||||
chr1:92345379
|
T | TA | 16 | a0001c0001t0002g0069a0001c0001t0002g0108a0001c0001t0003g0072others(13): Show | 16 | HG01070.hp2 HG01123.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.1620-445dupA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 92345379 | |||||
chr1:92345379
|
TA | T | 62 | a0001c0001t0002g0113a0001c0001t0037g0115a0001c0001t0039g0087others(59): Show | 63 | HG00280.hp2 HG00438.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.1620-445delA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 92345379 | |||||
chr1:92345379
|
TAA | T | 13 | a0001c0002t0001g0022a0001c0002t0001g0034a0001c0004t0008g0168others(10): Show | 13 | HG01070.hp1 HG01261.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1620-446_1620-445d others(4): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 92345379 | |||||
chr1:92345379
|
TAAA | T | 12 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(9): Show | 14 | HG01081.hp2 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1620-447_1620-445d others(5): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 92345379 | |||||
chr1:92345400
|
A | G | 2 | a0001c0005t0023g0152a0001c0005t0023g0156 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1620-446A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92345400 | ||||||
chr1:92345736
|
A | T | 7 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(4): Show | 9 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1620-110A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92345736 | ||||||
chr1:92345789
|
A | G | 1 | a0001c0045t0054g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1620-57A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 10/12 | chr1 | 92345789 | ||||||
chr1:92345934
|
TTAACTC | T | 3 | a0001c0020t0018g0160a0001c0020t0018g0161a0001c0046t0055g0162 | 3 | HG02145.hp2 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1688+24_1688+29del others(6): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92345934 | |||||
chr1:92346053
|
A | G | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1688+139A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92346053 | ||||||
chr1:92346169
|
GT | G | 43 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(40): Show | 45 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.1688+267delT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92346169 | |||||
chr1:92346245
|
C | T | 1 | a0002c0047t0069g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1688+331C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92346245 | ||||||
chr1:92346280
|
C | T | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1688+366C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92346280 | ||||||
chr1:92346310
|
C | T | 7 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(4): Show | 9 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1688+396C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92346310 | ||||||
chr1:92346524
|
C | T | 1 | a0001c0002t0001g0050 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1688+610C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92346524 | ||||||
chr1:92346613
|
T | G | 4 | a0001c0001t0002g0069a0001c0001t0002g0108a0001c0001t0004g0103others(1): Show | 4 | HG01070.hp2 HG01123.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1688+699T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92346613 | ||||||
chr1:92346639
|
A | G | 58 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(55): Show | 58 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1688+725A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92346639 | ||||||
chr1:92346722
|
A | C | 1 | a0001c0010t0002g0124 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1688+808A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92346722 | ||||||
chr1:92347328
|
AATATCAG others(3): Show |
A | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1688+1415_1688+142 others(14): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92347328 | ||||||
chr1:92347568
|
A | C | 20 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(17): Show | 22 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1688+1654A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92347568 | ||||||
chr1:92347921
|
T | C | 1 | a0001c0024t0007g0176 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1688+2007T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92347921 | ||||||
chr1:92348105
|
G | A | 1 | a0002c0048t0011g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1688+2191G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92348105 | ||||||
chr1:92348110
|
C | T | 1 | a0001c0002t0001g0019 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1688+2196C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92348110 | ||||||
chr1:92348141
|
G | A | 4 | a0001c0009t0007g0172a0001c0009t0007g0173a0001c0009t0007g0175others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1688+2227G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92348141 | ||||||
chr1:92348184
|
C | T | 43 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(40): Show | 44 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.1688+2270C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92348184 | ||||||
chr1:92348323
|
C | G | 1 | a0001c0008t0006g0058 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1688+2409C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92348323 | ||||||
chr1:92348324
|
T | G | 1 | a0001c0008t0006g0058 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1688+2410T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92348324 | ||||||
chr1:92348637
|
T | C | 2 | a0001c0005t0021g0154a0001c0005t0071g0157 | 2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1688+2723T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92348637 | ||||||
chr1:92348914
|
G | C | 6 | a0001c0008t0006g0013a0001c0008t0006g0014a0001c0008t0006g0056others(3): Show | 6 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(3): Show |
intron_variant | MODIFIER | c.1688+3000G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92348914 | ||||||
chr1:92348923
|
C | T | 1 | a0001c0011t0038g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1688+3009C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92348923 | ||||||
chr1:92348970
|
TATAAAG | T | 42 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(39): Show | 43 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.1688+3058_1688+306 others(10): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92348970 | |||||
chr1:92349031
|
A | G | 1 | a0001c0028t0061g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1688+3117A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92349031 | ||||||
chr1:92349166
|
C | A | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1688+3252C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92349166 | ||||||
chr1:92349241
|
A | G | 2 | a0001c0020t0018g0160a0001c0020t0018g0161 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1688+3327A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92349241 | ||||||
chr1:92349678
|
A | G | 1 | a0001c0001t0040g0104 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1688+3764A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92349678 | ||||||
chr1:92349837
|
A | C | 1 | a0001c0006t0005g0178 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1688+3923A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92349837 | ||||||
chr1:92350060
|
C | T | 1 | a0001c0045t0054g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1688+4146C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92350060 | ||||||
chr1:92350074
|
C | A | 43 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(40): Show | 44 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.1688+4160C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92350074 | ||||||
chr1:92350305
|
T | C | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1688+4391T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92350305 | ||||||
chr1:92350350
|
T | C | 1 | a0001c0033t0047g0060 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1688+4436T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92350350 | ||||||
chr1:92350488
|
T | G | 1 | a0003c0049t0070g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1688+4574T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92350488 | ||||||
chr1:92350591
|
T | C | 181 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(178): Show | 185 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1688+4677T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92350591 | ||||||
chr1:92350675
|
C | T | 1 | a0001c0001t0002g0141 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1688+4761C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92350675 | ||||||
chr1:92351075
|
G | A | 2 | a0001c0020t0018g0160a0001c0020t0018g0161 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1688+5161G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92351075 | ||||||
chr1:92351210
|
G | A | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1688+5296G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92351210 | ||||||
chr1:92351288
|
C | G | 4 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0053g0167others(1): Show | 4 | HG02280.hp2 HG06807.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1688+5374C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92351288 | ||||||
chr1:92351289
|
G | A | 86 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(83): Show | 87 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1688+5375G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92351289 | ||||||
chr1:92351305
|
C | CAAAAAAA others(5): Show |
1 | a0001c0006t0005g0179 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1688+5403_1688+541 others(16): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92351305 | |||||
chr1:92351305
|
C | CAAAAAAA others(6): Show |
3 | a0001c0006t0005g0178a0001c0006t0005g0183a0001c0006t0005g0184 | 3 | HG02630.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1688+5402_1688+541 others(17): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92351305 | |||||
chr1:92351305
|
C | CAAAAAAA others(7): Show |
2 | a0001c0006t0005g0182a0001c0023t0005g0181 | 2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1688+5401_1688+541 others(18): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92351305 | |||||
chr1:92351305
|
C | CAAAAAAA others(8): Show |
2 | a0001c0006t0005g0180a0001c0022t0005g0177 | 2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1688+5400_1688+541 others(19): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92351305 | |||||
chr1:92351305
|
CA | C | 28 | a0001c0001t0002g0093a0001c0001t0003g0079a0001c0001t0032g0091others(25): Show | 28 | HG00642.hp1 HG00741.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.1688+5414delA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92351305 | |||||
chr1:92351305
|
CAA | C | 76 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(73): Show | 77 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1688+5413_1688+541 others(6): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92351305 | |||||
chr1:92351305
|
CAAAAAAA others(5): Show |
C | 15 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(12): Show | 17 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1688+5403_1688+541 others(16): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92351305 | |||||
chr1:92351359
|
T | C | 15 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(12): Show | 17 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1688+5445T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92351359 | ||||||
chr1:92351391
|
T | C | 1 | a0001c0039t0002g0123 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1688+5477T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92351391 | ||||||
chr1:92351550
|
T | C | 9 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1688+5636T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92351550 | ||||||
chr1:92351880
|
C | T | 3 | a0001c0009t0007g0172a0001c0009t0007g0173a0001c0009t0024g0174 | 3 | HG02258.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1688+5966C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92351880 | ||||||
chr1:92351999
|
T | G | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1688+6085T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92351999 | ||||||
chr1:92352211
|
G | A | 6 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1688+6297G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92352211 | ||||||
chr1:92352309
|
C | T | 3 | a0001c0020t0018g0160a0001c0020t0018g0161a0001c0046t0055g0162 | 3 | HG02145.hp2 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1688+6395C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92352309 | ||||||
chr1:92352363
|
C | T | 1 | a0002c0047t0069g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1688+6449C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92352363 | ||||||
chr1:92352448
|
GT | G | 181 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(178): Show | 185 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1688+6543delT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92352448 | |||||
chr1:92352879
|
C | A | 1 | a0001c0001t0032g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1688+6965C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92352879 | ||||||
chr1:92353313
|
A | T | 42 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(39): Show | 44 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.1688+7399A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92353313 | ||||||
chr1:92353956
|
T | C | 1 | a0001c0006t0005g0178 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1688+8042T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92353956 | ||||||
chr1:92354026
|
A | G | 1 | a0001c0044t0057g0159 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1688+8112A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92354026 | ||||||
chr1:92354087
|
G | A | 1 | a0001c0001t0003g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1688+8173G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92354087 | ||||||
chr1:92354463
|
T | G | 51 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(48): Show | 52 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.1688+8549T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92354463 | ||||||
chr1:92354838
|
G | A | 1 | a0001c0034t0002g0128 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1688+8924G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92354838 | ||||||
chr1:92354889
|
A | ATAT | 2 | a0001c0006t0005g0179a0001c0006t0005g0183 | 2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1688+8975_1688+897 others(7): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92354889 | ||||||
chr1:92354890
|
A | AATT | 16 | a0001c0001t0003g0080a0001c0006t0005g0178a0001c0006t0005g0180others(13): Show | 16 | HG01243.hp1 HG02145.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1688+9004_1688+900 others(7): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92354890 | |||||
chr1:92354890
|
A | T | 2 | a0001c0006t0005g0179a0001c0006t0005g0183 | 2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1688+8976A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92354890 | ||||||
chr1:92354890
|
AATT | A | 9 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1688+9004_1688+900 others(7): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92354890 | |||||
chr1:92355107
|
T | A | 1 | a0001c0008t0006g0057 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1688+9193T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92355107 | ||||||
chr1:92355108
|
G | T | 1 | a0001c0008t0006g0057 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1688+9194G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92355108 | ||||||
chr1:92355622
|
A | T | 4 | a0001c0001t0002g0137a0001c0001t0002g0143a0001c0001t0056g0097others(1): Show | 4 | HG00423.hp1 HG00438.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1688+9708A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92355622 | ||||||
chr1:92355817
|
G | A | 181 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(178): Show | 185 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1688+9903G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92355817 | ||||||
chr1:92355894
|
A | G | 1 | a0001c0033t0047g0060 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1688+9980A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92355894 | ||||||
chr1:92355991
|
A | T | 5 | a0001c0009t0007g0172a0001c0009t0007g0173a0001c0009t0007g0175others(2): Show | 5 | HG02258.hp2 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1688+10077A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92355991 | ||||||
chr1:92356034
|
T | G | 1 | a0001c0044t0057g0159 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1688+10120T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92356034 | ||||||
chr1:92356114
|
C | T | 2 | a0001c0001t0049g0070a0001c0001t0050g0112 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1688+10200C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92356114 | ||||||
chr1:92356142
|
A | T | 1 | a0001c0005t0021g0154 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1688+10228A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92356142 | ||||||
chr1:92356273
|
A | C | 1 | a0001c0028t0061g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1688+10359A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92356273 | ||||||
chr1:92356280
|
T | C | 2 | a0001c0001t0049g0070a0001c0001t0050g0112 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1688+10366T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92356280 | ||||||
chr1:92356409
|
A | G | 1 | a0001c0034t0002g0128 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1688+10495A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92356409 | ||||||
chr1:92356582
|
C | T | 8 | a0001c0005t0021g0153a0001c0005t0021g0154a0001c0005t0022g0150others(5): Show | 8 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1688+10668C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92356582 | ||||||
chr1:92356585
|
A | ATTG | 11 | a0001c0001t0002g0143a0001c0001t0003g0079a0001c0001t0016g0075others(8): Show | 11 | HG00438.hp2 HG02080.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1688+10673_1688+10 others(9): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92356585 | |||||
chr1:92356585
|
AT | A | 20 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(17): Show | 20 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1688+10690delT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92356585 | |||||
chr1:92356585
|
ATT | A | 9 | a0001c0005t0021g0153a0001c0005t0021g0154a0001c0005t0022g0150others(6): Show | 9 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1688+10689_1688+10 others(8): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92356585 | |||||
chr1:92356586
|
T | TTG | 87 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(84): Show | 88 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1688+10673_1688+10 others(8): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92356586 | |||||
chr1:92356587
|
T | TG | 42 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(39): Show | 45 | HG00741.hp2 HG01069.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.1688+10673_1688+10 others(7): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92356587 | ||||||
chr1:92356588
|
T | G | 10 | a0001c0014t0029g0016a0001c0014t0030g0015a0001c0020t0018g0160others(7): Show | 10 | HG02109.hp2 HG02486.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1688+10674T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92356588 | ||||||
chr1:92356590
|
T | G | 8 | a0001c0005t0021g0153a0001c0005t0021g0154a0001c0005t0022g0150others(5): Show | 8 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1688+10676T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92356590 | ||||||
chr1:92356789
|
G | A | 8 | a0001c0004t0017g0164a0001c0004t0017g0165a0001c0004t0052g0166others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1688+10875G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92356789 | ||||||
chr1:92356997
|
C | G | 1 | a0001c0045t0054g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1688+11083C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92356997 | ||||||
chr1:92357094
|
T | TAC | 95 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(92): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1688+11206_1688+11 others(8): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92357094 | |||||
chr1:92357094
|
T | TACAC | 24 | a0001c0001t0002g0143a0001c0005t0021g0153a0001c0005t0021g0154others(21): Show | 24 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1688+11204_1688+11 others(10): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92357094 | |||||
chr1:92357094
|
T | TACACACA others(1): Show |
7 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(4): Show | 9 | HG01891.hp2 HG02280.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.1688+11200_1688+11 others(14): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92357094 | |||||
chr1:92357094
|
T | TACACACA others(3): Show |
1 | a0001c0003t0072g0149 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1688+11198_1688+11 others(16): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92357094 | |||||
chr1:92357094
|
TAC | T | 8 | a0001c0014t0029g0016a0001c0014t0030g0015a0002c0013t0011g0011others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1688+11206_1688+11 others(8): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92357094 | |||||
chr1:92357313
|
C | T | 14 | a0001c0001t0003g0003a0001c0001t0003g0071a0001c0001t0003g0079others(11): Show | 15 | HG00099.hp1 HG01243.hp1 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.1688+11399C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92357313 | ||||||
chr1:92357632
|
A | G | 42 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(39): Show | 43 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.1688+11718A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92357632 | ||||||
chr1:92358041
|
G | C | 173 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(170): Show | 177 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.1688+12127G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92358041 | ||||||
chr1:92358141
|
G | C | 63 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(60): Show | 66 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.1688+12227G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92358141 | ||||||
chr1:92358240
|
C | T | 1 | a0001c0001t0045g0142 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1688+12326C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92358240 | ||||||
chr1:92358414
|
CTT | C | 6 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1688+12502_1688+12 others(8): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92358414 | |||||
chr1:92358497
|
T | C | 6 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1688+12583T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92358497 | ||||||
chr1:92358761
|
A | G | 3 | a0001c0020t0018g0160a0001c0020t0018g0161a0001c0046t0055g0162 | 3 | HG02145.hp2 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1688+12847A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92358761 | ||||||
chr1:92358929
|
A | G | 1 | a0001c0001t0016g0075 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1688+13015A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92358929 | ||||||
chr1:92359080
|
C | G | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1688+13166C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92359080 | ||||||
chr1:92359369
|
G | T | 42 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(39): Show | 43 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.1688+13455G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92359369 | ||||||
chr1:92359515
|
T | C | 47 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(44): Show | 48 | HG00438.hp1 HG00642.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.1688+13601T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92359515 | ||||||
chr1:92359931
|
G | A | 1 | a0001c0002t0001g0050 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1688+14017G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92359931 | ||||||
chr1:92360002
|
AT | A | 181 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(178): Show | 185 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1688+14091delT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92360002 | |||||
chr1:92360004
|
T | G | 181 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(178): Show | 185 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1688+14090T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92360004 | ||||||
chr1:92360293
|
G | A | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1688+14379G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92360293 | ||||||
chr1:92360296
|
G | A | 1 | a0001c0014t0029g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1688+14382G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92360296 | ||||||
chr1:92360404
|
A | C | 1 | a0001c0007t0004g0102 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1688+14490A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92360404 | ||||||
chr1:92360543
|
G | A | 181 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(178): Show | 185 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1688+14629G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92360543 | ||||||
chr1:92360545
|
TAGAC | T | 3 | a0001c0009t0007g0172a0001c0009t0007g0173a0001c0009t0024g0174 | 3 | HG02258.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1688+14634_1688+14 others(10): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92360545 | |||||
chr1:92360674
|
T | C | 1 | a0001c0033t0047g0060 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1688+14760T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92360674 | ||||||
chr1:92360984
|
T | G | 1 | a0001c0002t0001g0031 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1688+15070T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92360984 | ||||||
chr1:92361002
|
C | T | 1 | a0001c0007t0004g0067 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1688+15088C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92361002 | ||||||
chr1:92361007
|
C | T | 1 | a0001c0001t0003g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1688+15093C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92361007 | ||||||
chr1:92361093
|
A | T | 1 | a0001c0044t0057g0159 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1688+15179A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92361093 | ||||||
chr1:92361094
|
T | A | 1 | a0001c0044t0057g0159 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1688+15180T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92361094 | ||||||
chr1:92361104
|
C | T | 1 | a0001c0044t0057g0159 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1688+15190C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92361104 | ||||||
chr1:92361106
|
C | T | 1 | a0001c0044t0057g0159 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1688+15192C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92361106 | ||||||
chr1:92361116
|
CAT | C | 172 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(169): Show | 174 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.1688+15216_1688+15 others(8): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92361116 | |||||
chr1:92361118
|
T | C | 1 | a0001c0044t0057g0159 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1688+15204T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92361118 | ||||||
chr1:92361130
|
T | C | 7 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(4): Show | 9 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1688+15216T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92361130 | ||||||
chr1:92361138
|
C | T | 7 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(4): Show | 9 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1688+15224C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92361138 | ||||||
chr1:92361140
|
T | A | 7 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(4): Show | 9 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1688+15226T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92361140 | ||||||
chr1:92361142
|
A | C | 7 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(4): Show | 9 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1688+15228A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92361142 | ||||||
chr1:92361159
|
G | A | 1 | a0001c0002t0001g0017 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1688+15245G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92361159 | ||||||
chr1:92361458
|
G | A | 1 | a0001c0028t0061g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1688+15544G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92361458 | ||||||
chr1:92361723
|
T | C | 1 | a0001c0007t0004g0067 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1688+15809T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92361723 | ||||||
chr1:92361850
|
T | TTTCTC | 87 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(84): Show | 90 | HG00438.hp1 HG00642.hp1 HG00741.hp1 others(87): Show |
intron_variant | MODIFIER | c.1688+15940_1688+15 others(11): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92361850 | |||||
chr1:92362252
|
T | C | 1 | a0001c0005t0073g0155 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1688+16338T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92362252 | ||||||
chr1:92362275
|
A | G | 1 | a0001c0002t0001g0028 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1688+16361A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92362275 | ||||||
chr1:92362476
|
G | C | 1 | a0001c0001t0043g0084 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1688+16562G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92362476 | ||||||
chr1:92362478
|
C | T | 1 | a0001c0001t0043g0084 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1688+16564C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92362478 | ||||||
chr1:92362834
|
G | A | 7 | a0001c0005t0021g0153a0001c0005t0021g0154a0001c0005t0022g0150others(4): Show | 7 | HG01069.hp2 HG01081.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1688+16920G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92362834 | ||||||
chr1:92362948
|
A | C | 25 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(22): Show | 26 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1688+17034A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92362948 | ||||||
chr1:92362982
|
C | T | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1688+17068C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92362982 | ||||||
chr1:92363169
|
C | T | 9 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1688+17255C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92363169 | ||||||
chr1:92363348
|
G | A | 2 | a0001c0016t0020g0106a0001c0016t0020g0135 | 2 | HG00642.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1689-17376G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92363348 | ||||||
chr1:92363556
|
G | A | 42 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(39): Show | 43 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.1689-17168G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92363556 | ||||||
chr1:92363581
|
T | C | 1 | a0001c0002t0001g0040 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1689-17143T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92363581 | ||||||
chr1:92363637
|
C | T | 4 | a0001c0009t0007g0172a0001c0009t0007g0173a0001c0009t0007g0175others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689-17087C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92363637 | ||||||
chr1:92363661
|
A | T | 3 | a0001c0009t0007g0172a0001c0009t0007g0173a0001c0009t0024g0174 | 3 | HG02258.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1689-17063A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92363661 | ||||||
chr1:92363913
|
G | A | 1 | a0001c0005t0073g0155 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1689-16811G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92363913 | ||||||
chr1:92363953
|
G | T | 1 | a0001c0020t0018g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1689-16771G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92363953 | ||||||
chr1:92364384
|
G | T | 9 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0077others(6): Show | 9 | HG01081.hp1 HG01261.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.1689-16340G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92364384 | ||||||
chr1:92364450
|
C | T | 1 | a0001c0001t0003g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1689-16274C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92364450 | ||||||
chr1:92364533
|
A | C | 1 | a0001c0001t0036g0187 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1689-16191A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92364533 | ||||||
chr1:92364658
|
T | C | 2 | a0001c0001t0002g0065a0001c0001t0002g0066 | 2 | HG00280.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1689-16066T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92364658 | ||||||
chr1:92365143
|
C | T | 6 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689-15581C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92365143 | ||||||
chr1:92365394
|
T | TA | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1689-15323dupA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92365394 | |||||
chr1:92366012
|
G | A | 46 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0069others(43): Show | 46 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.1689-14712G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92366012 | ||||||
chr1:92366376
|
T | C | 4 | a0001c0001t0002g0069a0001c0001t0002g0108a0001c0001t0004g0103others(1): Show | 4 | HG01070.hp2 HG01123.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689-14348T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92366376 | ||||||
chr1:92366622
|
C | G | 181 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(178): Show | 185 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1689-14102C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92366622 | ||||||
chr1:92366690
|
A | C | 44 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(41): Show | 45 | HG00438.hp1 HG00642.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.1689-14034A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92366690 | ||||||
chr1:92367042
|
G | A | 1 | a0001c0010t0002g0083 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1689-13682G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92367042 | ||||||
chr1:92367218
|
T | TTAAG | 3 | a0001c0012t0010g0027a0001c0012t0010g0037a0001c0012t0010g0039 | 3 | HG00741.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1689-13504_1689-13 others(10): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92367218 | |||||
chr1:92367343
|
G | A | 1 | a0001c0042t0058g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689-13381G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92367343 | ||||||
chr1:92367583
|
T | A | 1 | a0001c0005t0021g0153 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1689-13141T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92367583 | ||||||
chr1:92367884
|
A | G | 4 | a0001c0001t0032g0091a0001c0001t0043g0084a0001c0018t0003g0085others(1): Show | 4 | HG02738.hp2 HG04115.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689-12840A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92367884 | ||||||
chr1:92368196
|
C | T | 8 | a0001c0014t0029g0016a0001c0014t0030g0015a0002c0013t0011g0011others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1689-12528C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92368196 | ||||||
chr1:92368646
|
T | C | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1689-12078T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92368646 | ||||||
chr1:92368664
|
G | A | 1 | a0001c0042t0058g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689-12060G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92368664 | ||||||
chr1:92369283
|
T | C | 2 | a0001c0005t0023g0152a0001c0005t0023g0156 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1689-11441T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92369283 | ||||||
chr1:92369673
|
G | A | 1 | a0001c0032t0033g0134 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1689-11051G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92369673 | ||||||
chr1:92369708
|
TAAAC | T | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1689-11014_1689-11 others(10): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92369708 | |||||
chr1:92369859
|
A | C | 1 | a0001c0005t0073g0155 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1689-10865A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92369859 | ||||||
chr1:92370085
|
A | T | 1 | a0001c0001t0002g0137 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1689-10639A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92370085 | ||||||
chr1:92370160
|
C | T | 9 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1689-10564C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92370160 | ||||||
chr1:92370301
|
T | A | 43 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(40): Show | 44 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.1689-10423T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92370301 | ||||||
chr1:92370432
|
G | T | 17 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(14): Show | 17 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1689-10292G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92370432 | ||||||
chr1:92370455
|
A | G | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1689-10269A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92370455 | ||||||
chr1:92370593
|
G | A | 7 | a0001c0005t0021g0153a0001c0005t0021g0154a0001c0005t0022g0150others(4): Show | 7 | HG01069.hp2 HG01081.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689-10131G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92370593 | ||||||
chr1:92370716
|
C | G | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1689-10008C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92370716 | ||||||
chr1:92370998
|
T | C | 1 | a0001c0005t0023g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1689-9726T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92370998 | ||||||
chr1:92371029
|
G | A | 1 | a0001c0001t0044g0082 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1689-9695G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92371029 | ||||||
chr1:92371169
|
G | T | 1 | a0001c0033t0047g0060 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1689-9555G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92371169 | ||||||
chr1:92371304
|
CA | C | 11 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(8): Show | 11 | HG01069.hp2 HG01081.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.1689-9404delA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92371304 | |||||
chr1:92371304
|
CAAA | C | 9 | a0001c0006t0005g0178a0001c0006t0005g0179a0001c0006t0005g0180others(6): Show | 9 | HG02630.hp2 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1689-9406_1689-940 others(7): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92371304 | |||||
chr1:92371311
|
AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0002g0137a0001c0033t0047g0060 | 2 | HG00423.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1689-9411_1689-940 others(16): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92371311 | |||||
chr1:92371313
|
AAAAAAAA others(5): Show |
A | 81 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(78): Show | 82 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1689-9409_1689-939 others(16): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92371313 | |||||
chr1:92371315
|
A | T | 2 | a0001c0002t0001g0022a0001c0002t0059g0047 | 2 | HG01106.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1689-9409A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92371315 | ||||||
chr1:92371315
|
AAAAAATA others(5): Show |
A | 3 | a0001c0001t0004g0116a0001c0017t0002g0068a0001c0019t0034g0088 | 3 | HG01070.hp2 HG02738.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1689-9407_1689-939 others(16): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92371315 | |||||
chr1:92371317
|
A | ATATATAT others(12): Show |
1 | a0001c0003t0012g0145 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1689-9407_1689-940 others(23): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92371317 | ||||||
chr1:92371317
|
A | T | 34 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(31): Show | 35 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.1689-9407A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92371317 | ||||||
chr1:92371319
|
A | ATATATAT others(10): Show |
6 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(3): Show | 8 | HG02055.hp2 HG02280.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.1689-9405_1689-940 others(21): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92371319 | ||||||
chr1:92371319
|
A | T | 52 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(49): Show | 53 | HG00438.hp1 HG00642.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.1689-9405A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92371319 | ||||||
chr1:92371320
|
AT | A | 2 | a0001c0005t0023g0156a0001c0008t0006g0059 | 2 | HG01516.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1689-9403delT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92371320 | ||||||
chr1:92371320
|
ATAT | A | 7 | a0001c0004t0017g0164a0001c0004t0017g0165a0001c0004t0052g0166others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1689-9403_1689-940 others(7): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92371320 | ||||||
chr1:92371321
|
T | A | 6 | a0001c0008t0006g0013a0001c0008t0006g0014a0001c0008t0006g0057others(3): Show | 6 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689-9403T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92371321 | ||||||
chr1:92371366
|
G | A | 1 | a0001c0004t0008g0169 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1689-9358G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92371366 | ||||||
chr1:92371755
|
A | G | 1 | a0001c0003t0072g0149 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1689-8969A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92371755 | ||||||
chr1:92371805
|
T | C | 1 | a0001c0044t0057g0159 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1689-8919T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92371805 | ||||||
chr1:92371889
|
C | CA | 108 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(105): Show | 111 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1689-8816dupA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92371889 | |||||
chr1:92371889
|
C | CAA | 13 | a0001c0001t0013g0073a0001c0001t0032g0091a0001c0003t0072g0149others(10): Show | 13 | HG01106.hp1 HG01109.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1689-8817_1689-881 others(6): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92371889 | |||||
chr1:92371909
|
C | A | 4 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(1): Show | 4 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689-8815C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92371909 | ||||||
chr1:92372392
|
G | A | 4 | a0001c0001t0002g0069a0001c0001t0002g0108a0001c0001t0004g0103others(1): Show | 4 | HG01070.hp2 HG01123.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689-8332G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92372392 | ||||||
chr1:92372404
|
G | A | 1 | a0001c0001t0004g0006 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1689-8320G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92372404 | ||||||
chr1:92372542
|
T | C | 1 | a0001c0001t0002g0137 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1689-8182T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92372542 | ||||||
chr1:92372808
|
T | C | 15 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(12): Show | 17 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1689-7916T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92372808 | ||||||
chr1:92372921
|
C | T | 42 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(39): Show | 44 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.1689-7803C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92372921 | ||||||
chr1:92373046
|
G | A | 1 | a0001c0038t0048g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1689-7678G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92373046 | ||||||
chr1:92373158
|
CAAAG | C | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1689-7561_1689-755 others(8): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92373158 | |||||
chr1:92373194
|
AT | A | 130 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(127): Show | 133 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.1689-7525delT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92373194 | |||||
chr1:92373472
|
T | C | 1 | a0001c0001t0027g0122 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1689-7252T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92373472 | ||||||
chr1:92373482
|
C | T | 43 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(40): Show | 44 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.1689-7242C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92373482 | ||||||
chr1:92373733
|
T | TA | 18 | a0001c0001t0002g0065a0001c0001t0002g0108a0001c0001t0002g0125others(15): Show | 18 | HG00280.hp1 HG00423.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1689-6986dupA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92373733 | |||||
chr1:92373733
|
T | TAA | 5 | a0001c0001t0002g0133a0001c0001t0014g0078a0001c0007t0051g0099others(2): Show | 5 | HG01361.hp2 HG03486.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1689-6987_1689-698 others(6): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92373733 | |||||
chr1:92373733
|
T | TAAA | 15 | a0001c0001t0002g0005a0001c0001t0002g0077a0001c0001t0003g0003others(12): Show | 16 | HG01261.hp2 HG01516.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.1689-6988_1689-698 others(7): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92373733 | |||||
chr1:92373733
|
T | TAAAA | 8 | a0001c0001t0003g0071a0001c0001t0015g0138a0001c0001t0044g0082others(5): Show | 8 | HG00099.hp1 HG01081.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1689-6989_1689-698 others(8): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92373733 | |||||
chr1:92373733
|
T | TAAAAA | 6 | a0001c0001t0003g0079a0001c0001t0003g0080a0001c0001t0003g0107others(3): Show | 6 | HG01243.hp1 HG02738.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1689-6990_1689-698 others(9): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92373733 | |||||
chr1:92373733
|
TAAAAATA others(3): Show |
T | 1 | a0001c0042t0058g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1689-6985_1689-697 others(14): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92373733 | |||||
chr1:92373733
|
TAAAAATA others(4): Show |
T | 2 | a0001c0001t0002g0141a0001c0001t0002g0143 | 2 | HG02080.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1689-6985_1689-697 others(15): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92373733 | |||||
chr1:92373733
|
TAAAAATA others(5): Show |
T | 2 | a0001c0001t0013g0073a0001c0017t0002g0101 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1689-6985_1689-697 others(16): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92373733 | |||||
chr1:92373733
|
TAAAAATA others(6): Show |
T | 1 | a0001c0001t0003g0072 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1689-6985_1689-697 others(17): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92373733 | |||||
chr1:92373733
|
TAAAAATA others(10): Show |
T | 1 | a0001c0001t0002g0113 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1689-6985_1689-696 others(21): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92373733 | |||||
chr1:92373739
|
T | A | 84 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(81): Show | 85 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1689-6985T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92373739 | ||||||
chr1:92373739
|
TA | T | 36 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(33): Show | 37 | HG00639.hp1 HG01069.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.1689-6954delA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92373739 | |||||
chr1:92373739
|
TAA | T | 13 | a0001c0002t0001g0026a0001c0002t0001g0034a0001c0003t0009g0001others(10): Show | 15 | HG01070.hp1 HG01169.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1689-6955_1689-695 others(6): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92373739 | |||||
chr1:92373739
|
TAAA | T | 10 | a0001c0005t0021g0153a0001c0005t0021g0154a0001c0005t0022g0150others(7): Show | 10 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1689-6956_1689-695 others(7): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92373739 | |||||
chr1:92373739
|
TAAAA | T | 21 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(18): Show | 21 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1689-6957_1689-695 others(8): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92373739 | |||||
chr1:92373745
|
A | T | 8 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(5): Show | 10 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1689-6979A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92373745 | ||||||
chr1:92373746
|
A | T | 1 | a0001c0002t0001g0024 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1689-6978A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92373746 | ||||||
chr1:92373747
|
A | T | 1 | a0001c0044t0057g0159 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1689-6977A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92373747 | ||||||
chr1:92373748
|
A | T | 8 | a0001c0005t0021g0153a0001c0005t0021g0154a0001c0005t0022g0150others(5): Show | 8 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1689-6976A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92373748 | ||||||
chr1:92373751
|
A | T | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1689-6973A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92373751 | ||||||
chr1:92373753
|
A | T | 3 | a0001c0020t0018g0160a0001c0020t0018g0161a0001c0046t0055g0162 | 3 | HG02145.hp2 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1689-6971A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92373753 | ||||||
chr1:92373754
|
A | T | 7 | a0001c0005t0021g0153a0001c0005t0021g0154a0001c0005t0022g0150others(4): Show | 7 | HG01069.hp2 HG01081.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689-6970A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92373754 | ||||||
chr1:92373760
|
A | T | 1 | a0001c0005t0021g0153 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1689-6964A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92373760 | ||||||
chr1:92373855
|
G | T | 1 | a0001c0033t0047g0060 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1689-6869G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92373855 | ||||||
chr1:92373864
|
A | G | 1 | a0001c0007t0031g0105 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1689-6860A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92373864 | ||||||
chr1:92374021
|
C | G | 1 | a0001c0019t0034g0088 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1689-6703C>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92374021 | ||||||
chr1:92374102
|
T | A | 4 | a0001c0004t0017g0164a0001c0004t0017g0165a0001c0004t0052g0166others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689-6622T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92374102 | ||||||
chr1:92374221
|
G | A | 7 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(4): Show | 9 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1689-6503G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92374221 | ||||||
chr1:92374323
|
C | A | 1 | a0001c0002t0001g0050 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1689-6401C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92374323 | ||||||
chr1:92374399
|
T | C | 1 | a0001c0001t0004g0103 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1689-6325T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92374399 | ||||||
chr1:92374433
|
A | G | 1 | a0001c0001t0002g0065 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1689-6291A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92374433 | ||||||
chr1:92374756
|
C | T | 1 | a0001c0008t0006g0057 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1689-5968C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92374756 | ||||||
chr1:92375019
|
G | C | 1 | a0001c0001t0043g0084 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1689-5705G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92375019 | ||||||
chr1:92375443
|
C | T | 1 | a0001c0002t0065g0023 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1689-5281C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92375443 | ||||||
chr1:92375475
|
G | A | 1 | a0001c0046t0055g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1689-5249G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92375475 | ||||||
chr1:92375613
|
T | C | 1 | a0001c0005t0022g0150 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1689-5111T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92375613 | ||||||
chr1:92375700
|
G | A | 2 | a0001c0018t0003g0085a0001c0018t0003g0118 | 2 | NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1689-5024G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92375700 | ||||||
chr1:92375709
|
T | A | 1 | a0001c0007t0004g0067 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1689-5015T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92375709 | ||||||
chr1:92375709
|
T | C | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1689-5015T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92375709 | ||||||
chr1:92375831
|
AAAAC | A | 8 | a0001c0006t0005g0178a0001c0006t0005g0179a0001c0006t0005g0180others(5): Show | 8 | HG02630.hp2 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1689-4881_1689-487 others(8): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92375831 | |||||
chr1:92375925
|
A | G | 2 | a0001c0011t0002g0130a0001c0011t0038g0094 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1689-4799A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92375925 | ||||||
chr1:92375956
|
C | T | 1 | a0001c0028t0061g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1689-4768C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92375956 | ||||||
chr1:92375999
|
C | CA | 8 | a0001c0001t0013g0073a0001c0001t0032g0091a0001c0002t0001g0051others(5): Show | 8 | HG01123.hp1 HG01175.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1689-4706dupA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92375999 | |||||
chr1:92375999
|
CA | C | 28 | a0001c0002t0001g0026a0001c0004t0008g0163a0001c0004t0008g0168others(25): Show | 28 | HG01069.hp2 HG01169.hp1 HG01943.hp2 others(25): Show |
intron_variant | MODIFIER | c.1689-4706delA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92375999 | |||||
chr1:92376066
|
T | C | 1 | a0001c0001t0043g0084 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1689-4658T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92376066 | ||||||
chr1:92376070
|
C | T | 9 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0077others(6): Show | 9 | HG01081.hp1 HG01261.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.1689-4654C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92376070 | ||||||
chr1:92376111
|
T | C | 20 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(17): Show | 22 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1689-4613T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92376111 | ||||||
chr1:92376301
|
T | C | 1 | a0001c0019t0013g0126 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1689-4423T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92376301 | ||||||
chr1:92376345
|
G | T | 2 | a0001c0004t0017g0165a0001c0004t0052g0166 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1689-4379G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92376345 | ||||||
chr1:92376434
|
C | T | 3 | a0001c0001t0003g0079a0001c0001t0003g0080a0001c0001t0044g0082 | 3 | HG00099.hp1 HG01243.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1689-4290C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92376434 | ||||||
chr1:92376711
|
T | C | 130 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(127): Show | 133 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.1689-4013T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92376711 | ||||||
chr1:92377291
|
C | T | 5 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(2): Show | 5 | HG02280.hp2 HG06807.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1689-3433C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92377291 | ||||||
chr1:92377356
|
T | C | 2 | a0001c0001t0014g0110a0001c0001t0039g0087 | 2 | HG01517.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1689-3368T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92377356 | ||||||
chr1:92377516
|
CA | C | 32 | a0001c0002t0001g0002a0001c0002t0001g0019a0001c0002t0001g0022others(29): Show | 35 | HG00438.hp1 HG00741.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.1689-3184delA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92377516 | |||||
chr1:92377516
|
CAA | C | 144 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(141): Show | 145 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.1689-3185_1689-318 others(6): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92377516 | |||||
chr1:92377587
|
G | C | 5 | a0001c0009t0007g0172a0001c0009t0007g0173a0001c0009t0007g0175others(2): Show | 5 | HG02258.hp2 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1689-3137G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92377587 | ||||||
chr1:92377621
|
G | A | 42 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(39): Show | 44 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.1689-3103G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92377621 | ||||||
chr1:92378035
|
T | C | 1 | a0001c0046t0055g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1689-2689T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92378035 | ||||||
chr1:92378184
|
T | TATTC | 11 | a0001c0001t0002g0069a0001c0001t0002g0093a0001c0002t0001g0051others(8): Show | 11 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1689-2508_1689-250 others(8): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92378184 | |||||
chr1:92378184
|
TATTC | T | 3 | a0001c0001t0016g0075a0001c0020t0018g0160a0001c0020t0018g0161 | 3 | HG02145.hp2 HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1689-2508_1689-250 others(8): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92378184 | |||||
chr1:92378184
|
TATTCATT others(1): Show |
T | 2 | a0001c0001t0004g0186a0001c0044t0057g0159 | 2 | HG03195.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1689-2512_1689-250 others(12): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92378184 | |||||
chr1:92378562
|
A | T | 1 | a0001c0045t0054g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1689-2162A>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92378562 | ||||||
chr1:92378705
|
T | G | 1 | a0001c0005t0021g0153 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1689-2019T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92378705 | ||||||
chr1:92378818
|
A | G | 6 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689-1906A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92378818 | ||||||
chr1:92379046
|
C | T | 1 | a0001c0008t0006g0013 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1689-1678C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92379046 | ||||||
chr1:92379273
|
T | A | 20 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(17): Show | 22 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1689-1451T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92379273 | ||||||
chr1:92379573
|
G | A | 42 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(39): Show | 44 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.1689-1151G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92379573 | ||||||
chr1:92379737
|
C | A | 1 | a0001c0046t0055g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1689-987C>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92379737 | ||||||
chr1:92380023
|
GCTGAGGC others(11): Show |
G | 45 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(42): Show | 46 | HG00438.hp1 HG00642.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.1689-675_1689-658d others(20): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92380023 | |||||
chr1:92380107
|
G | A | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1689-617G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92380107 | ||||||
chr1:92380115
|
C | CA | 4 | a0001c0001t0002g0108a0001c0005t0073g0155a0001c0010t0002g0083others(1): Show | 4 | HG01109.hp1 HG01123.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689-602dupA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92380115 | |||||
chr1:92380278
|
CA | C | 39 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(36): Show | 41 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1689-433delA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 92380278 | |||||
chr1:92380460
|
T | C | 8 | a0001c0006t0005g0178a0001c0006t0005g0179a0001c0006t0005g0180others(5): Show | 8 | HG02630.hp2 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1689-264T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 11/12 | chr1 | 92380460 | ||||||
chr1:92381026
|
A | G | 42 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(39): Show | 44 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.1838+153A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92381026 | ||||||
chr1:92381124
|
G | A | 181 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(178): Show | 185 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1838+251G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92381124 | ||||||
chr1:92381129
|
G | A | 1 | a0001c0022t0005g0177 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1838+256G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92381129 | ||||||
chr1:92381218
|
G | A | 1 | a0001c0027t0046g0117 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1838+345G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92381218 | ||||||
chr1:92381234
|
C | T | 6 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1838+361C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92381234 | ||||||
chr1:92381240
|
G | C | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1838+367G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92381240 | ||||||
chr1:92381269
|
T | A | 53 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(50): Show | 54 | HG00438.hp1 HG00642.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1838+396T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92381269 | ||||||
chr1:92381403
|
C | T | 128 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(125): Show | 131 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1838+530C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92381403 | ||||||
chr1:92381445
|
C | T | 1 | a0001c0031t0001g0064 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1838+572C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92381445 | ||||||
chr1:92381588
|
C | CT | 25 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(22): Show | 27 | HG01069.hp1 HG01069.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.1838+731dupT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr1 | 92381588 | |||||
chr1:92381588
|
C | CTT | 136 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(133): Show | 138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.1838+730_1838+731d others(4): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr1 | 92381588 | |||||
chr1:92381588
|
C | CTTT | 14 | a0001c0009t0007g0172a0001c0009t0007g0173a0001c0009t0007g0175others(11): Show | 14 | HG00438.hp2 HG00642.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1838+729_1838+731d others(5): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr1 | 92381588 | |||||
chr1:92381762
|
A | AT | 15 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(12): Show | 17 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1838+897dupT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr1 | 92381762 | |||||
chr1:92381765
|
T | A | 4 | a0001c0010t0002g0076a0001c0010t0002g0081a0001c0010t0002g0083others(1): Show | 4 | HG01081.hp1 HG01261.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1838+892T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92381765 | ||||||
chr1:92381770
|
T | A | 3 | a0001c0012t0010g0027a0001c0012t0010g0037a0001c0012t0010g0039 | 3 | HG00741.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1838+897T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92381770 | ||||||
chr1:92381944
|
G | A | 1 | a0001c0032t0033g0134 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1838+1071G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92381944 | ||||||
chr1:92381988
|
C | T | 4 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(1): Show | 4 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1838+1115C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92381988 | ||||||
chr1:92382001
|
T | C | 8 | a0001c0007t0004g0067a0001c0007t0004g0102a0001c0007t0004g0127others(5): Show | 8 | HG00642.hp2 HG01106.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.1838+1128T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92382001 | ||||||
chr1:92382275
|
G | T | 1 | a0001c0040t0002g0119 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1838+1402G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92382275 | ||||||
chr1:92382340
|
G | A | 1 | a0001c0028t0061g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1838+1467G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92382340 | ||||||
chr1:92382408
|
T | C | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1838+1535T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92382408 | ||||||
chr1:92382490
|
T | G | 1 | a0001c0033t0047g0060 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1838+1617T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92382490 | ||||||
chr1:92382513
|
A | C | 1 | a0001c0039t0002g0123 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1838+1640A>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92382513 | ||||||
chr1:92382540
|
A | G | 15 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(12): Show | 17 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1838+1667A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92382540 | ||||||
chr1:92382542
|
G | A | 1 | a0001c0023t0005g0181 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1838+1669G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92382542 | ||||||
chr1:92382548
|
T | G | 1 | a0001c0023t0005g0181 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1838+1675T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92382548 | ||||||
chr1:92382791
|
T | G | 1 | a0001c0034t0002g0128 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1838+1918T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92382791 | ||||||
chr1:92382840
|
G | A | 2 | a0001c0044t0057g0159a0001c0045t0054g0158 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1838+1967G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92382840 | ||||||
chr1:92382893
|
T | C | 1 | a0001c0042t0058g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1838+2020T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92382893 | ||||||
chr1:92383087
|
G | A | 1 | a0003c0049t0070g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1838+2214G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92383087 | ||||||
chr1:92383278
|
T | C | 1 | a0001c0039t0002g0123 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1838+2405T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92383278 | ||||||
chr1:92383323
|
T | G | 2 | a0001c0029t0064g0043a0001c0033t0047g0060 | 2 | HG01891.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1838+2450T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92383323 | ||||||
chr1:92383331
|
T | A | 2 | a0002c0047t0069g0010a0003c0049t0070g0009 | 2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1838+2458T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92383331 | ||||||
chr1:92383672
|
C | T | 2 | a0001c0014t0029g0016a0001c0014t0030g0015 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1838+2799C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92383672 | ||||||
chr1:92383673
|
G | A | 6 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1838+2800G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92383673 | ||||||
chr1:92383722
|
T | C | 1 | a0001c0035t0002g0121 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1838+2849T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92383722 | ||||||
chr1:92383743
|
T | C | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1838+2870T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92383743 | ||||||
chr1:92383744
|
G | GA | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1838+2872dupA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr1 | 92383744 | |||||
chr1:92383749
|
C | T | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1838+2876C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92383749 | ||||||
chr1:92383752
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G | T | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1838+2879G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92383752 | ||||||
chr1:92383796
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G | A | 187 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1838+2923G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92383796 | ||||||
chr1:92383962
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A | G | 47 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(44): Show | 48 | HG00438.hp1 HG00642.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.1839-3049A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92383962 | ||||||
chr1:92383967
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C | CT | 165 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1839-3033dupT | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr1 | 92383967 | |||||
chr1:92383967
|
C | CTT | 21 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(18): Show | 23 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1839-3034_1839-303 others(6): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr1 | 92383967 | |||||
chr1:92383984
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G | A | 3 | a0001c0018t0003g0085a0001c0018t0003g0118a0001c0027t0046g0117 | 3 | HG03516.hp2 NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1839-3027G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92383984 | ||||||
chr1:92384100
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G | A | 1 | a0001c0036t0041g0095 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1839-2911G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92384100 | ||||||
chr1:92384130
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G | T | 1 | a0001c0030t0001g0018 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1839-2881G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92384130 | ||||||
chr1:92384133
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T | A | 1 | a0001c0024t0007g0176 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1839-2878T>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92384133 | ||||||
chr1:92384492
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C | T | 8 | a0001c0005t0021g0153a0001c0005t0021g0154a0001c0005t0022g0150others(5): Show | 8 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1839-2519C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92384492 | ||||||
chr1:92384623
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C | CA | 8 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(5): Show | 10 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1839-2373dupA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr1 | 92384623 | |||||
chr1:92384929
|
C | T | 22 | a0001c0004t0008g0163a0001c0004t0008g0168a0001c0004t0008g0169others(19): Show | 22 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1839-2082C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92384929 | ||||||
chr1:92384930
|
GCTTGAGC others(152): Show |
G | 1 | a0001c0028t0061g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1839-2066_1839-190 others(4): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr1 | 92384930 | |||||
chr1:92385173
|
CA | C | 158 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(155): Show | 160 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1839-1821delA | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr1 | 92385173 | |||||
chr1:92385173
|
CAA | C | 7 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(4): Show | 7 | HG01256.hp1 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1839-1822_1839-182 others(6): Show |
RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr1 | 92385173 | |||||
chr1:92385291
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A | G | 2 | a0001c0019t0013g0126a0001c0019t0034g0088 | 2 | HG02738.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1839-1720A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92385291 | ||||||
chr1:92385294
|
T | C | 2 | a0001c0016t0020g0106a0001c0016t0020g0135 | 2 | HG00642.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1839-1717T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92385294 | ||||||
chr1:92385604
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A | G | 9 | a0001c0003t0009g0001a0001c0003t0009g0147a0001c0003t0012g0001others(6): Show | 11 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1839-1407A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92385604 | ||||||
chr1:92385848
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C | T | 6 | a0002c0013t0011g0011a0002c0013t0011g0012a0002c0013t0068g0008others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1839-1163C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92385848 | ||||||
chr1:92385977
|
T | C | 1 | a0001c0037t0003g0140 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1839-1034T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92385977 | ||||||
chr1:92386140
|
T | G | 1 | a0001c0046t0055g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1839-871T>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92386140 | ||||||
chr1:92386614
|
G | C | 1 | a0001c0045t0054g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1839-397G>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92386614 | ||||||
chr1:92386826
|
G | A | 3 | a0001c0020t0018g0160a0001c0020t0018g0161a0001c0046t0055g0162 | 3 | HG02145.hp2 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1839-185G>A | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92386826 | ||||||
chr1:92386833
|
T | C | 44 | a0001c0002t0001g0002a0001c0002t0001g0017a0001c0002t0001g0019others(41): Show | 45 | HG00438.hp1 HG00642.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.1839-178T>C | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92386833 | ||||||
chr1:92386856
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A | G | 1 | a0001c0038t0048g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1839-155A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92386856 | ||||||
chr1:92386876
|
G | T | 1 | a0001c0034t0002g0128 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1839-135G>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92386876 | ||||||
chr1:92386921
|
C | T | 1 | a0001c0044t0057g0159 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1839-90C>T | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92386921 | ||||||
chr1:92386947
|
A | G | 181 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0065others(178): Show | 185 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1839-64A>G | RPAP2 | ENSG00000122484.9 | transcript | ENST00000610020.2 | protein_coding | 12/12 | chr1 | 92386947 |