geneid | 79682 |
---|---|
ensemblid | ENSG00000151725.12 |
hgncid | 21348 |
symbol | CENPU |
name | centromere protein U |
refseq_nuc | NM_024629.4 |
refseq_prot | NP_078905.2 |
ensembl_nuc | ENST00000281453.10 |
ensembl_prot | ENSP00000281453.5 |
mane_status | MANE Select |
chr | chr4 |
start | 184694085 |
end | 184734096 |
strand | - |
ver | v1.2 |
region | chr4:184694085-184734096 |
region5000 | chr4:184689085-184739096 |
regionname0 | CENPU_chr4_184694085_184734096 |
regionname5000 | CENPU_chr4_184689085_184739096 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 418 | 158 | 46 | 23 | 64 | 8 | 15 | 56 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0002 | 0/0 | 418 | 126 | 5 | 22 | 88 | 3 | 8 | 66 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0003 | 0/0 | 418 | 22 | 15 | 5 | 0 | 0 | 2 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0004 | 0/0 | 418 | 18 | 16 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0005 | 0/0 | 418 | 18 | 5 | 8 | 0 | 0 | 5 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0006 | 0/0 | 418 | 10 | 2 | 6 | 0 | 1 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0007 | 0/0 | 418 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0008 | 0/0 | 389 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0009 | 0/0 | 418 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0010 | 0/0 | 418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1257 | 158 | 46 | 23 | 64 | 8 | 15 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
c0002 | 0/0 | 1257 | 125 | 4 | 22 | 88 | 3 | 8 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
c0003 | 0/0 | 1257 | 19 | 15 | 4 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
c0004 | 0/0 | 1257 | 18 | 16 | 2 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
c0005 | 0/0 | 1257 | 14 | 1 | 8 | 0 | 0 | 5 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
c0006 | 0/0 | 1257 | 10 | 2 | 6 | 0 | 1 | 1 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
c0007 | 0/0 | 1257 | 4 | 4 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
c0008 | 0/0 | 1257 | 3 | 0 | 1 | 0 | 0 | 2 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
c0009 | 0/0 | 1257 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
c0010 | 0/0 | 1257 | 2 | 0 | 0 | 0 | 0 | 2 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
c0011 | 0/0 | 1257 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
c0012 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
c0013 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1238 | 150 | 39 | 23 | 61 | 8 | 17 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
t0002 | 0/0 | 1242 | 119 | 5 | 20 | 83 | 3 | 8 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
t0003 | 0/0 | 1229 | 23 | 19 | 4 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
t0004 | 0/0 | 1234 | 16 | 0 | 9 | 0 | 0 | 7 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
t0005 | 0/0 | 1238 | 11 | 3 | 6 | 0 | 1 | 1 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
t0006 | 0/0 | 1242 | 8 | 8 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
t0007 | 0/0 | 1242 | 7 | 5 | 1 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
t0008 | 0/0 | 1238 | 6 | 0 | 2 | 3 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
t0009 | 0/0 | 1234 | 5 | 5 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
t0010 | 0/0 | 1238 | 3 | 3 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
t0011 | 0/0 | 1242 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
t0012 | 0/0 | 1242 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
t0013 | 0/0 | 1238 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
t0014 | 0/0 | 1234 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
t0015 | 0/0 | 1238 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
t0016 | 0/0 | 1238 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
t0017 | 0/0 | 1238 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0002 | 0/0 | 7 | 0 | 0 | 4 | 0 | 3 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0003 | 0/0 | 7 | 0 | 3 | 0 | 0 | 4 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0006 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0007 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0019 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0250 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1257 | 158 | 46 | 23 | 64 | 8 | 15 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0002c0002 | 0/0 | 1257 | 125 | 4 | 22 | 88 | 3 | 8 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0002c0012 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0003c0003 | 0/0 | 1257 | 19 | 15 | 4 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0003c0008 | 0/0 | 1257 | 3 | 0 | 1 | 0 | 0 | 2 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0004c0004 | 0/0 | 1257 | 18 | 16 | 2 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0005c0005 | 0/0 | 1257 | 14 | 1 | 8 | 0 | 0 | 5 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0005c0007 | 0/0 | 1257 | 4 | 4 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0006c0006 | 0/0 | 1257 | 10 | 2 | 6 | 0 | 1 | 1 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0007c0010 | 0/0 | 1257 | 2 | 0 | 0 | 0 | 0 | 2 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0008c0009 | 0/0 | 1257 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0009c0011 | 0/0 | 1257 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0010c0013 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2494 | 132 | 26 | 22 | 59 | 8 | 15 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0001c0001t0002 | 0/0 | 2498 | 3 | 1 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0001c0001t0006 | 0/0 | 2498 | 8 | 8 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0001c0001t0007 | 0/0 | 2498 | 6 | 4 | 1 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0001c0001t0010 | 0/0 | 2494 | 3 | 3 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0001c0001t0012 | 0/0 | 2498 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0001c0001t0013 | 0/0 | 2494 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0001c0001t0015 | 0/0 | 2494 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0001c0001t0017 | 0/0 | 2494 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0002c0002t0001 | 0/0 | 2494 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0002c0002t0002 | 0/0 | 2498 | 115 | 4 | 20 | 81 | 3 | 7 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0002c0002t0008 | 0/0 | 2494 | 6 | 0 | 2 | 3 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0002c0002t0011 | 0/0 | 2498 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0002c0012t0007 | 0/0 | 2498 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0003c0003t0003 | 0/0 | 2485 | 19 | 15 | 4 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0003c0008t0004 | 0/0 | 2490 | 3 | 0 | 1 | 0 | 0 | 2 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0004c0004t0001 | 0/0 | 2494 | 12 | 11 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0004c0004t0009 | 0/0 | 2490 | 5 | 5 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0004c0004t0014 | 0/0 | 2490 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0005c0005t0004 | 0/0 | 2490 | 13 | 0 | 8 | 0 | 0 | 5 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0005c0005t0016 | 0/0 | 2494 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0005c0007t0003 | 0/0 | 2485 | 4 | 4 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0006c0006t0005 | 0/0 | 2494 | 10 | 2 | 6 | 0 | 1 | 1 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0007c0010t0001 | 0/0 | 2494 | 2 | 0 | 0 | 0 | 0 | 2 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0008c0009t0001 | 0/0 | 2494 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0009c0011t0002 | 0/0 | 2498 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
a0010c0013t0005 | 0/0 | 2494 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | copy fasta | chr4 | 184689085 | 184739096 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0250 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0006g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0006g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0006g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0007g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0007g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0007g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0007g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0010g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0010g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0012g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0012g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0013g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0013g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0015g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0001c0001t0017g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0001 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0002 | 0/0 | 7 | 0 | 0 | 4 | 0 | 3 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0006 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0007 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0008g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0008g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0008g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0008g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0008g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0008g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0011g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0002t0011g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0002c0012t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0003t0003g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0003t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0003t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0003t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0003t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0003t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0003t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0003t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0003t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0003t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0003t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0003t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0003t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0003t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0003t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0003t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0003t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0008t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0008t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0003c0008t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0004c0004t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0004c0004t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0004c0004t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0004c0004t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0004c0004t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0004c0004t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0004c0004t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0004c0004t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0004c0004t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0004c0004t0009g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0004c0004t0009g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0004c0004t0009g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0004c0004t0009g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0004c0004t0009g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0004c0004t0014g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0005c0005t0004g0003 | 0/0 | 7 | 0 | 3 | 0 | 0 | 4 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0005c0005t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0005c0005t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0005c0005t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0005c0005t0004g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0005c0005t0004g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0005c0005t0004g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0005c0005t0016g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0005c0007t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0005c0007t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0005c0007t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0005c0007t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0006c0006t0005g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0006c0006t0005g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0006c0006t0005g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0006c0006t0005g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0006c0006t0005g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0006c0006t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0006c0006t0005g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0007c0010t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0007c0010t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0008c0009t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0009c0011t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
a0010c0013t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | GBR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | GBR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00280 | hp1 | a0002 | c0002 | t0002 | g0112 | EUR | FIN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | FIN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | CHS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | CHS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | CHS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | CHS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | CHS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00639 | hp2 | a0006 | c0006 | t0005 | g0008 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00642 | hp1 | a0005 | c0005 | t0004 | g0003 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | CHS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0056 | EAS | CHS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00733 | hp1 | a0004 | c0004 | t0001 | g0300 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00733 | hp2 | a0006 | c0006 | t0005 | g0008 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00735 | hp1 | a0005 | c0005 | t0004 | g0287 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0077 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0122 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01074 | hp1 | a0003 | c0003 | t0003 | g0026 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01074 | hp2 | a0006 | c0006 | t0005 | g0008 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01081 | hp1 | a0003 | c0003 | t0003 | g0278 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01109 | hp1 | a0003 | c0003 | t0003 | g0268 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01167 | hp1 | a0003 | c0003 | t0003 | g0272 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01167 | hp2 | a0006 | c0006 | t0005 | g0129 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01169 | hp1 | a0006 | c0006 | t0005 | g0126 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01243 | hp1 | a0005 | c0005 | t0004 | g0303 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01243 | hp2 | a0002 | c0002 | t0002 | g0012 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01256 | hp1 | a0005 | c0005 | t0004 | g0003 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0064 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0012 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0054 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01261 | hp2 | a0002 | c0002 | t0002 | g0014 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0113 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01358 | hp2 | a0005 | c0005 | t0004 | g0289 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0057 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01433 | hp2 | a0006 | c0006 | t0005 | g0128 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01496 | hp1 | a0003 | c0008 | t0004 | g0157 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | IBS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | IBS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0007 | EUR | IBS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0007 | EUR | IBS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | IBS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01884 | hp1 | a0003 | c0003 | t0003 | g0279 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0259 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01891 | hp2 | a0002 | c0012 | t0007 | g0131 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01928 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0065 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01952 | hp1 | a0002 | c0002 | t0008 | g0067 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01975 | hp1 | a0002 | c0002 | t0002 | g0052 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01975 | hp2 | a0004 | c0004 | t0014 | g0295 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01993 | hp2 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02004 | hp1 | a0002 | c0002 | t0008 | g0062 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02004 | hp2 | a0002 | c0002 | t0002 | g0102 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02055 | hp1 | a0005 | c0005 | t0016 | g0286 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02071 | hp1 | a0002 | c0002 | t0008 | g0087 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0254 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02145 | hp2 | a0004 | c0004 | t0001 | g0292 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02148 | hp1 | a0005 | c0005 | t0004 | g0288 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0045 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02165 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | CDX | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02165 | hp2 | a0001 | c0001 | t0013 | g0176 | EAS | CDX | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02258 | hp2 | a0001 | c0001 | t0007 | g0258 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02273 | hp1 | a0005 | c0005 | t0004 | g0285 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02273 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02280 | hp2 | a0005 | c0007 | t0003 | g0283 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02293 | hp2 | a0002 | c0002 | t0002 | g0034 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02300 | hp2 | a0001 | c0001 | t0007 | g0257 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02451 | hp2 | a0006 | c0006 | t0005 | g0016 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02523 | hp2 | a0002 | c0002 | t0008 | g0032 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02572 | hp2 | a0004 | c0004 | t0009 | g0297 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02615 | hp1 | a0003 | c0003 | t0003 | g0270 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0107 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02622 | hp1 | a0003 | c0003 | t0003 | g0276 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02622 | hp2 | a0004 | c0004 | t0001 | g0291 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02630 | hp1 | a0001 | c0001 | t0015 | g0203 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02630 | hp2 | a0004 | c0004 | t0001 | g0030 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02647 | hp1 | a0004 | c0004 | t0009 | g0293 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0265 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02717 | hp2 | a0004 | c0004 | t0001 | g0299 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02723 | hp2 | a0003 | c0003 | t0003 | g0246 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02735 | hp2 | a0005 | c0005 | t0004 | g0003 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02809 | hp2 | a0005 | c0007 | t0003 | g0282 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02895 | hp2 | a0004 | c0004 | t0001 | g0029 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0264 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02897 | hp1 | a0004 | c0004 | t0001 | g0029 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02897 | hp2 | a0001 | c0001 | t0006 | g0261 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02922 | hp1 | a0003 | c0003 | t0003 | g0027 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02922 | hp2 | a0004 | c0004 | t0009 | g0294 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02965 | hp1 | a0001 | c0001 | t0006 | g0263 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02965 | hp2 | a0004 | c0004 | t0001 | g0028 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02970 | hp1 | a0006 | c0006 | t0005 | g0016 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02970 | hp2 | a0001 | c0001 | t0010 | g0146 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02976 | hp1 | a0003 | c0003 | t0003 | g0026 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0118 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0050 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03041 | hp2 | a0004 | c0004 | t0001 | g0301 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03098 | hp2 | a0002 | c0002 | t0002 | g0104 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03130 | hp1 | a0001 | c0001 | t0010 | g0145 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03130 | hp2 | a0003 | c0003 | t0003 | g0269 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03139 | hp1 | a0008 | c0009 | t0001 | g0011 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03139 | hp2 | a0005 | c0007 | t0003 | g0281 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03195 | hp1 | a0003 | c0003 | t0003 | g0267 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03209 | hp1 | a0001 | c0001 | t0012 | g0252 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03225 | hp1 | a0004 | c0004 | t0001 | g0302 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03225 | hp2 | a0003 | c0003 | t0003 | g0275 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03453 | hp1 | a0003 | c0003 | t0003 | g0245 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03486 | hp2 | a0001 | c0001 | t0007 | g0255 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03491 | hp1 | a0005 | c0005 | t0004 | g0003 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0116 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0117 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03516 | hp2 | a0001 | c0001 | t0017 | g0149 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03540 | hp1 | a0003 | c0003 | t0003 | g0027 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03579 | hp1 | a0004 | c0004 | t0001 | g0030 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03579 | hp2 | a0008 | c0009 | t0001 | g0011 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03688 | hp1 | a0007 | c0010 | t0001 | g0139 | SAS | STU | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03688 | hp2 | a0006 | c0006 | t0005 | g0130 | SAS | STU | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03704 | hp1 | a0005 | c0005 | t0004 | g0003 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03710 | hp1 | a0009 | c0011 | t0002 | g0053 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03710 | hp2 | a0007 | c0010 | t0001 | g0137 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03927 | hp1 | a0003 | c0008 | t0004 | g0249 | SAS | BEB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG04184 | hp1 | a0003 | c0008 | t0004 | g0242 | SAS | BEB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG04184 | hp2 | a0002 | c0002 | t0008 | g0042 | SAS | BEB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | STU | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG04204 | hp2 | a0005 | c0005 | t0004 | g0003 | SAS | STU | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG04228 | hp2 | a0005 | c0005 | t0004 | g0290 | SAS | STU | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18522 | hp1 | a0004 | c0004 | t0001 | g0028 | AFR | YRI | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0260 | AFR | YRI | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | CHB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18906 | hp2 | a0001 | c0001 | t0010 | g0148 | AFR | YRI | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18940 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18949 | hp1 | a0002 | c0002 | t0008 | g0046 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18949 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18952 | hp2 | a0001 | c0001 | t0007 | g0235 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18961 | hp2 | a0002 | c0002 | t0011 | g0109 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18970 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18971 | hp1 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18972 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18972 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18974 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18980 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18986 | hp1 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18988 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18990 | hp1 | a0001 | c0001 | t0013 | g0193 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18991 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18992 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18993 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19001 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19003 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19006 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19007 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19010 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19030 | hp1 | a0010 | c0013 | t0005 | g0125 | AFR | LWK | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | LWK | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0068 | AFR | LWK | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19043 | hp2 | a0004 | c0004 | t0009 | g0296 | AFR | LWK | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19054 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19060 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19064 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19072 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19074 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19075 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19076 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19077 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19079 | hp1 | a0002 | c0002 | t0011 | g0108 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19079 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19083 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19086 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19089 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19240 | hp1 | a0005 | c0007 | t0003 | g0284 | AFR | YRI | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA19240 | hp2 | a0003 | c0003 | t0003 | g0271 | AFR | YRI | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA20129 | hp1 | a0003 | c0003 | t0003 | g0274 | AFR | ASW | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ASW | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA20805 | hp1 | a0006 | c0006 | t0005 | g0127 | EUR | TSI | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | TSI | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | GIH | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | GIH | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01123 | hp1 | a0005 | c0005 | t0004 | g0003 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0051 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02109 | hp1 | a0003 | c0003 | t0003 | g0277 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02486 | hp1 | a0004 | c0004 | t0009 | g0298 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03471 | hp1 | a0001 | c0001 | t0012 | g0253 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | USA | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
HG06807 | hp2 | a0002 | c0002 | t0002 | g0006 | AFR | USA | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA21309 | hp1 | a0001 | c0001 | t0006 | g0262 | AFR | LWK | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
NA21309 | hp2 | a0003 | c0003 | t0003 | g0273 | AFR | LWK | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0214 | REF | REF | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0250 | REF | REF | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:184702404
|
C | T | 1 | a0004 | 18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
missense_variant | MODERATE | c.835G>A | p.Ala279Thr | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 9/13 | 869/2494 | 835/1257 | 279/418 | chr4 | 184702404 | ||
chr4:184702410
|
C | A | 1 | a0007 | 2 | HG03688.hp1 HG03710.hp2 |
missense_variant | MODERATE | c.829G>T | p.Ala277Ser | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 9/13 | 863/2494 | 829/1257 | 277/418 | chr4 | 184702410 | ||
chr4:184712989
|
A | G | 1 | a0009 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.643T>C | p.Ser215Pro | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/13 | 677/2494 | 643/1257 | 215/418 | chr4 | 184712989 | ||
chr4:184712990
|
T | C | 4 | a0003a0005a0006others(1): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
missense_variant | MODERATE | c.642A>G | p.Ile214Met | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/13 | 676/2494 | 642/1257 | 214/418 | chr4 | 184712990 | ||
chr4:184716509
|
G | A | 1 | a0010 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.506C>T | p.Ala169Val | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/13 | 540/2494 | 506/1257 | 169/418 | chr4 | 184716509 | ||
chr4:184716545
|
A | G | 4 | a0003a0005a0006others(1): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
missense_variant | MODERATE | c.470T>C | p.Ile157Thr | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/13 | 504/2494 | 470/1257 | 157/418 | chr4 | 184716545 | ||
chr4:184734017
|
C | T | 4 | a0002a0006a0009others(1): Show | 138 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(135): Show |
missense_variant&splice_region_variant | MODERATE | c.46G>A | p.Gly16Ser | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/13 | 80/2494 | 46/1257 | 16/418 | chr4 | 184734017 | ||
chr4:184734038
|
G | C | 2 | a0004a0005 | 36 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(33): Show |
missense_variant | MODERATE | c.25C>G | p.Pro9Ala | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/13 | 59/2494 | 25/1257 | 9/418 | chr4 | 184734038 | ||
chr4:184734060
|
C | T | 1 | a0008 | 2 | HG03139.hp1 HG03579.hp2 |
start_lost | HIGH | c.3G>A | p.Met1? | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/13 | 37/2494 | 3/1257 | 1/418 | chr4 | 184734060 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:184702375
|
T | C | 2 | a0003c0003a0005c0007 | 23 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
synonymous_variant | LOW | c.864A>G | p.Gln288Gln | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 9/13 | 898/2494 | 864/1257 | 288/418 | chr4 | 184702375 | ||
chr4:184729000
|
G | A | 6 | a0003c0003a0003c0008a0005c0005others(3): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
synonymous_variant | LOW | c.132C>T | p.Phe44Phe | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/13 | 166/2494 | 132/1257 | 44/418 | chr4 | 184729000 | ||
chr4:184734036
|
C | G | 2 | a0002c0002a0009c0011 | 126 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(123): Show |
synonymous_variant | LOW | c.27G>C | p.Pro9Pro | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/13 | 61/2494 | 27/1257 | 9/418 | chr4 | 184734036 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:184694173
|
G | T | 3 | a0001c0001t0015a0003c0003t0003a0005c0007t0003 | 24 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1115C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 1115 | chr4 | 184694173 | |||||
chr4:184694378
|
A | T | 8 | a0001c0001t0015a0003c0003t0003a0003c0008t0004others(5): Show | 52 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*910T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 910 | chr4 | 184694378 | |||||
chr4:184694404
|
T | G | 1 | a0005c0005t0016 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*884A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 884 | chr4 | 184694404 | |||||
chr4:184694413
|
G | GTATC | 8 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(5): Show | 138 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*871_*874dupGATA | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 874 | chr4 | 184694413 | |||||
chr4:184694461
|
C | G | 1 | a0002c0002t0011 | 2 | NA18961.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*827G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 827 | chr4 | 184694461 | |||||
chr4:184694537
|
ACAGATGA others(2): Show |
A | 2 | a0003c0003t0003a0005c0007t0003 | 23 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*742_*750delCTTCAT others(3): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 742 | chr4 | 184694537 | |||||
chr4:184694610
|
C | A | 9 | a0001c0001t0015a0001c0001t0017a0003c0003t0003others(6): Show | 53 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*678G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 678 | chr4 | 184694610 | |||||
chr4:184694614
|
T | G | 9 | a0001c0001t0015a0001c0001t0017a0003c0003t0003others(6): Show | 53 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*674A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 674 | chr4 | 184694614 | |||||
chr4:184694842
|
T | A | 1 | a0001c0001t0012 | 2 | HG03209.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*446A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 446 | chr4 | 184694842 | |||||
chr4:184694938
|
T | C | 1 | a0001c0001t0010 | 3 | HG02970.hp2 HG03130.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*350A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 350 | chr4 | 184694938 | |||||
chr4:184694966
|
G | A | 1 | a0004c0004t0014 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*322C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 322 | chr4 | 184694966 | |||||
chr4:184694970
|
TATTA | T | 2 | a0003c0008t0004a0005c0005t0004 | 16 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*314_*317delTAAT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 314 | chr4 | 184694970 | |||||
chr4:184695013
|
A | C | 8 | a0001c0001t0015a0003c0003t0003a0003c0008t0004others(5): Show | 52 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*275T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 275 | chr4 | 184695013 | |||||
chr4:184695065
|
TACTC | T | 2 | a0004c0004t0009a0004c0004t0014 | 6 | HG01975.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*219_*222delGAGT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 219 | chr4 | 184695065 | |||||
chr4:184695146
|
C | G | 1 | a0001c0001t0006 | 8 | HG02280.hp1 HG02717.hp1 HG02896.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*142G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 142 | chr4 | 184695146 | |||||
chr4:184695284
|
C | T | 6 | a0001c0001t0002a0001c0001t0012a0002c0002t0002others(3): Show | 129 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*4G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 4 | chr4 | 184695284 | |||||
chr4:184734096
|
T | G | 1 | a0001c0001t0013 | 2 | HG02165.hp2 NA18990.hp1 |
5_prime_UTR_variant | MODIFIER | c.-34A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/13 | 34 | chr4 | 184734096 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:184695415
|
A | G | 5 | a0001c0001t0015g0203a0005c0007t0003g0281a0005c0007t0003g0282others(2): Show | 5 | HG02280.hp2 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1144-14T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184695415 | ||||||
chr4:184695477
|
T | C | 41 | a0001c0001t0015g0203a0003c0003t0003g0026a0003c0003t0003g0027others(38): Show | 52 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.1144-76A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184695477 | ||||||
chr4:184695660
|
T | C | 41 | a0001c0001t0015g0203a0003c0003t0003g0026a0003c0003t0003g0027others(38): Show | 52 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.1144-259A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184695660 | ||||||
chr4:184695705
|
T | C | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1144-304A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184695705 | ||||||
chr4:184695851
|
C | T | 1 | a0002c0002t0002g0093 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1144-450G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184695851 | ||||||
chr4:184696191
|
C | G | 1 | a0001c0001t0001g0204 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1144-790G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696191 | ||||||
chr4:184696363
|
T | C | 2 | a0001c0001t0012g0252a0001c0001t0012g0253 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1144-962A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696363 | ||||||
chr4:184696371
|
A | G | 40 | a0001c0001t0015g0203a0003c0003t0003g0026a0003c0003t0003g0027others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1144-970T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696371 | ||||||
chr4:184696375
|
T | C | 41 | a0001c0001t0015g0203a0003c0003t0003g0026a0003c0003t0003g0027others(38): Show | 52 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.1144-974A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696375 | ||||||
chr4:184696482
|
T | G | 1 | a0001c0001t0001g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1144-1081A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696482 | ||||||
chr4:184696631
|
C | T | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1143+1016G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696631 | ||||||
chr4:184696693
|
T | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1143+954A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696693 | ||||||
chr4:184696694
|
A | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1143+953T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696694 | ||||||
chr4:184696699
|
T | TA | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1143+947_1143+948i others(3): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696699 | ||||||
chr4:184696781
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1143+866T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696781 | ||||||
chr4:184696845
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1143+802G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696845 | ||||||
chr4:184696883
|
C | CT | 95 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(92): Show | 110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1143+763dupA | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696883 | ||||||
chr4:184696883
|
C | T | 1 | a0004c0004t0001g0029 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1143+764G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696883 | ||||||
chr4:184696883
|
CT | C | 40 | a0002c0002t0002g0078a0003c0003t0003g0026a0003c0003t0003g0027others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1143+763delA | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696883 | ||||||
chr4:184696999
|
GCCT | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1143+645_1143+647d others(5): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696999 | ||||||
chr4:184697118
|
G | C | 1 | a0005c0005t0016g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1143+529C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697118 | ||||||
chr4:184697188
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1143+459A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697188 | ||||||
chr4:184697219
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1143+428G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697219 | ||||||
chr4:184697227
|
T | C | 1 | a0001c0001t0017g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1143+420A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697227 | ||||||
chr4:184697354
|
TCAATTGA others(65): Show |
T | 2 | a0001c0001t0001g0219a0001c0001t0001g0229 | 2 | HG00741.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1143+221_1143+292d others(74): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697354 | ||||||
chr4:184697425
|
C | T | 15 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0267others(12): Show | 17 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1143+222G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697425 | ||||||
chr4:184697452
|
C | T | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1143+195G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697452 | ||||||
chr4:184697468
|
G | A | 1 | a0001c0001t0012g0253 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1143+179C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697468 | ||||||
chr4:184697535
|
CTG | C | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1143+110_1143+111d others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697535 | ||||||
chr4:184697623
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1143+24C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697623 | ||||||
chr4:184697865
|
T | G | 1 | a0001c0001t0001g0241 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.987-62A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184697865 | ||||||
chr4:184697941
|
G | A | 7 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.987-138C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184697941 | ||||||
chr4:184698127
|
C | T | 47 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(44): Show | 58 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.987-324G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698127 | ||||||
chr4:184698128
|
A | G | 47 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(44): Show | 58 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.987-325T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698128 | ||||||
chr4:184698133
|
C | T | 1 | a0002c0002t0002g0052 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.987-330G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698133 | ||||||
chr4:184698206
|
A | G | 23 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(20): Show | 25 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.987-403T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698206 | ||||||
chr4:184698278
|
G | C | 1 | a0005c0005t0016g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.987-475C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698278 | ||||||
chr4:184698343
|
G | A | 23 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(20): Show | 25 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.987-540C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698343 | ||||||
chr4:184698413
|
A | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.987-610T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698413 | ||||||
chr4:184698447
|
G | A | 1 | a0002c0012t0007g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.987-644C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698447 | ||||||
chr4:184698466
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.987-663A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698466 | ||||||
chr4:184698511
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.987-708G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698511 | ||||||
chr4:184698512
|
G | A | 4 | a0004c0004t0001g0029a0004c0004t0001g0030a0004c0004t0001g0301others(1): Show | 6 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.987-709C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698512 | ||||||
chr4:184698549
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.987-746G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698549 | ||||||
chr4:184698607
|
G | A | 22 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(19): Show | 25 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.987-804C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698607 | ||||||
chr4:184698698
|
C | T | 1 | a0002c0002t0008g0042 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.987-895G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698698 | ||||||
chr4:184698738
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.987-935C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698738 | ||||||
chr4:184698792
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.987-989G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698792 | ||||||
chr4:184698813
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.987-1010T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698813 | ||||||
chr4:184698887
|
C | CT | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.987-1085_987-1084i others(3): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698887 | ||||||
chr4:184698954
|
G | T | 147 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0266others(144): Show | 181 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(178): Show |
intron_variant | MODIFIER | c.987-1151C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698954 | ||||||
chr4:184698959
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.987-1156A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698959 | ||||||
chr4:184699037
|
C | G | 107 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0266others(104): Show | 130 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.987-1234G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699037 | ||||||
chr4:184699055
|
C | T | 6 | a0001c0001t0002g0151a0002c0002t0002g0040a0002c0002t0002g0074others(3): Show | 6 | HG00621.hp1 HG02165.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.987-1252G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699055 | ||||||
chr4:184699102
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.987-1299G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699102 | ||||||
chr4:184699154
|
T | C | 1 | a0004c0004t0009g0298 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.987-1351A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699154 | ||||||
chr4:184699187
|
G | A | 114 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(111): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.987-1384C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699187 | ||||||
chr4:184699247
|
G | A | 114 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(111): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.987-1444C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699247 | ||||||
chr4:184699262
|
G | A | 1 | a0002c0002t0002g0110 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.987-1459C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699262 | ||||||
chr4:184699286
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.987-1483G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699286 | ||||||
chr4:184699309
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.987-1506C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699309 | ||||||
chr4:184699331
|
A | AAAAT | 3 | a0001c0001t0001g0133a0002c0002t0002g0048a0002c0002t0002g0100 | 3 | HG01993.hp1 HG02015.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.986+1485_986+1488d others(6): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699331 | ||||||
chr4:184699350
|
A | G | 21 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(18): Show | 23 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.986+1470T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699350 | ||||||
chr4:184699356
|
A | AAATAAAA others(1): Show |
39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.986+1463_986+1464i others(10): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699356 | ||||||
chr4:184699356
|
A | AAATAAAT others(9): Show |
1 | a0005c0005t0016g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.986+1463_986+1464i others(18): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699356 | ||||||
chr4:184699469
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.986+1351C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699469 | ||||||
chr4:184699597
|
C | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.986+1223G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699597 | ||||||
chr4:184699636
|
T | G | 1 | a0009c0011t0002g0053 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.986+1184A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699636 | ||||||
chr4:184699668
|
C | CTCTT | 17 | a0003c0008t0004g0157a0003c0008t0004g0242a0003c0008t0004g0249others(14): Show | 26 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.986+1151_986+1152i others(6): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699668 | ||||||
chr4:184699668
|
C | CTTTT | 22 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(19): Show | 24 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.986+1148_986+1151d others(6): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699668 | ||||||
chr4:184699746
|
C | T | 17 | a0002c0002t0002g0012a0002c0002t0002g0041a0002c0002t0002g0043others(14): Show | 18 | HG01243.hp2 HG01257.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.986+1074G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699746 | ||||||
chr4:184699863
|
G | A | 3 | a0001c0001t0010g0145a0001c0001t0010g0146a0001c0001t0010g0148 | 3 | HG02970.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.986+957C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699863 | ||||||
chr4:184699872
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.986+948C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699872 | ||||||
chr4:184699908
|
C | T | 1 | a0002c0002t0002g0063 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.986+912G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699908 | ||||||
chr4:184699952
|
C | T | 1 | a0001c0001t0017g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.986+868G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699952 | ||||||
chr4:184699968
|
T | A | 3 | a0004c0004t0009g0296a0004c0004t0009g0297a0004c0004t0014g0295 | 3 | HG01975.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.986+852A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699968 | ||||||
chr4:184699999
|
A | G | 2 | a0004c0004t0009g0293a0004c0004t0009g0294 | 2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.986+821T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699999 | ||||||
chr4:184700076
|
G | A | 1 | a0004c0004t0014g0295 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.986+744C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700076 | ||||||
chr4:184700095
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.986+725G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700095 | ||||||
chr4:184700212
|
C | T | 2 | a0001c0001t0006g0261a0001c0001t0006g0264 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.986+608G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700212 | ||||||
chr4:184700294
|
T | TAAC | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.986+523_986+525dup others(3): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700294 | ||||||
chr4:184700300
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.986+520T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700300 | ||||||
chr4:184700348
|
G | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0229 | 2 | HG00741.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.986+472C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700348 | ||||||
chr4:184700423
|
C | G | 104 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0017g0149others(101): Show | 127 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.986+397G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700423 | ||||||
chr4:184700514
|
CCAAGCAG others(2): Show |
C | 3 | a0001c0001t0010g0145a0001c0001t0010g0146a0001c0001t0010g0148 | 3 | HG02970.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.986+297_986+305del others(9): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700514 | ||||||
chr4:184700525
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.986+295T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700525 | ||||||
chr4:184700538
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.986+282A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700538 | ||||||
chr4:184700550
|
A | C | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.986+270T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700550 | ||||||
chr4:184700572
|
T | C | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.986+248A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700572 | ||||||
chr4:184700698
|
C | T | 1 | a0001c0001t0010g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.986+122G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700698 | ||||||
chr4:184700739
|
G | T | 1 | a0002c0002t0002g0050 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.986+81C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700739 | ||||||
chr4:184700771
|
A | T | 1 | a0003c0003t0003g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.986+49T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700771 | ||||||
chr4:184700892
|
C | T | 112 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(109): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.925-11G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184700892 | ||||||
chr4:184700917
|
G | A | 1 | a0002c0002t0002g0097 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.925-36C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184700917 | ||||||
chr4:184701173
|
A | C | 41 | a0001c0001t0015g0203a0003c0003t0003g0026a0003c0003t0003g0027others(38): Show | 52 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.925-292T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701173 | ||||||
chr4:184701248
|
A | G | 17 | a0003c0008t0004g0157a0003c0008t0004g0242a0003c0008t0004g0249others(14): Show | 26 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.925-367T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701248 | ||||||
chr4:184701279
|
A | C | 300 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(297): Show | 355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.925-398T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701279 | ||||||
chr4:184701355
|
T | C | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.925-474A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701355 | ||||||
chr4:184701366
|
C | T | 1 | a0001c0001t0001g0231 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.925-485G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701366 | ||||||
chr4:184701391
|
C | A | 1 | a0002c0002t0011g0109 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.925-510G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701391 | ||||||
chr4:184701625
|
A | G | 300 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(297): Show | 355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.924+464T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701625 | ||||||
chr4:184701805
|
C | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.924+284G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701805 | ||||||
chr4:184701871
|
C | T | 2 | a0004c0004t0001g0291a0004c0004t0001g0292 | 2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.924+218G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701871 | ||||||
chr4:184701981
|
T | G | 1 | a0003c0003t0003g0245 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.924+108A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701981 | ||||||
chr4:184702050
|
G | A | 1 | a0002c0002t0002g0060 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.924+39C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184702050 | ||||||
chr4:184702158
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.877-22G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 9/12 | chr4 | 184702158 | ||||||
chr4:184702207
|
A | C | 1 | a0002c0002t0002g0085 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.877-71T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 9/12 | chr4 | 184702207 | ||||||
chr4:184702557
|
TA | T | 41 | a0002c0002t0002g0078a0003c0003t0003g0026a0003c0003t0003g0027others(38): Show | 52 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.798-117delT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702557 | ||||||
chr4:184702634
|
T | C | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.798-193A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702634 | ||||||
chr4:184702691
|
A | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-250T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702691 | ||||||
chr4:184702763
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-322G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702763 | ||||||
chr4:184702809
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-368A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702809 | ||||||
chr4:184702819
|
C | T | 57 | a0001c0001t0001g0023a0001c0001t0001g0156a0001c0001t0001g0168others(54): Show | 69 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.798-378G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702819 | ||||||
chr4:184702822
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.798-381A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702822 | ||||||
chr4:184702835
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-394C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702835 | ||||||
chr4:184702866
|
C | T | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.798-425G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702866 | ||||||
chr4:184702893
|
G | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-452C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702893 | ||||||
chr4:184702975
|
G | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-534C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702975 | ||||||
chr4:184702996
|
C | T | 1 | a0002c0002t0008g0087 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.798-555G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702996 | ||||||
chr4:184703066
|
T | C | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.798-625A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703066 | ||||||
chr4:184703075
|
TG | T | 6 | a0003c0003t0003g0245a0003c0003t0003g0246a0005c0007t0003g0281others(3): Show | 6 | HG02280.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.798-635delC | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703075 | ||||||
chr4:184703084
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-643G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703084 | ||||||
chr4:184703127
|
A | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-686T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703127 | ||||||
chr4:184703182
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-741G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703182 | ||||||
chr4:184703234
|
T | C | 174 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(171): Show | 211 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(208): Show |
intron_variant | MODIFIER | c.798-793A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703234 | ||||||
chr4:184703246
|
T | C | 1 | a0001c0001t0017g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.798-805A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703246 | ||||||
chr4:184703385
|
ACTGCCTC others(4): Show |
A | 2 | a0001c0001t0001g0017a0001c0001t0001g0173 | 3 | HG01257.hp1 HG01258.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.798-955_798-945del others(11): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703385 | ||||||
chr4:184703426
|
G | A | 7 | a0001c0001t0006g0025a0001c0001t0006g0260a0001c0001t0006g0261others(4): Show | 8 | HG02280.hp1 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.798-985C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703426 | ||||||
chr4:184703444
|
T | C | 15 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0267others(12): Show | 17 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.798-1003A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703444 | ||||||
chr4:184703599
|
A | C | 9 | a0002c0002t0002g0005a0002c0002t0002g0015a0002c0002t0002g0072others(6): Show | 13 | HG02129.hp1 NA18747.hp1 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.798-1158T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703599 | ||||||
chr4:184703607
|
A | T | 1 | a0002c0012t0007g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.798-1166T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703607 | ||||||
chr4:184703796
|
T | C | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.798-1355A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703796 | ||||||
chr4:184703898
|
C | T | 15 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0267others(12): Show | 17 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.798-1457G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703898 | ||||||
chr4:184703965
|
G | A | 3 | a0001c0001t0010g0145a0001c0001t0010g0146a0001c0001t0010g0148 | 3 | HG02970.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.798-1524C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703965 | ||||||
chr4:184703969
|
TA | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-1529delT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703969 | ||||||
chr4:184704023
|
G | A | 2 | a0002c0002t0002g0058a0002c0002t0002g0063 | 2 | NA18960.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.798-1582C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704023 | ||||||
chr4:184704086
|
CTT | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-1647_798-1646d others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704086 | ||||||
chr4:184704193
|
C | T | 9 | a0002c0002t0002g0005a0002c0002t0002g0015a0002c0002t0002g0072others(6): Show | 13 | HG02129.hp1 NA18747.hp1 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.798-1752G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704193 | ||||||
chr4:184704236
|
C | T | 42 | a0001c0001t0010g0145a0001c0001t0010g0146a0001c0001t0010g0148others(39): Show | 53 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.798-1795G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704236 | ||||||
chr4:184704243
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-1802A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704243 | ||||||
chr4:184704369
|
T | C | 147 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0266others(144): Show | 181 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(178): Show |
intron_variant | MODIFIER | c.798-1928A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704369 | ||||||
chr4:184704383
|
T | C | 1 | a0002c0002t0002g0069 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.798-1942A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704383 | ||||||
chr4:184704445
|
G | A | 4 | a0001c0001t0007g0254a0001c0001t0007g0255a0001c0001t0007g0257others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.798-2004C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704445 | ||||||
chr4:184704503
|
A | G | 114 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(111): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.798-2062T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704503 | ||||||
chr4:184704516
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.798-2075A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704516 | ||||||
chr4:184704583
|
A | ACC | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.798-2143_798-2142i others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704583 | ||||||
chr4:184704584
|
C | CATATGAC others(7): Show |
1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.798-2144_798-2143i others(16): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704584 | ||||||
chr4:184704850
|
G | T | 106 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0266others(103): Show | 129 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.798-2409C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704850 | ||||||
chr4:184705225
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-2784T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705225 | ||||||
chr4:184705357
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-2916G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705357 | ||||||
chr4:184705388
|
G | A | 173 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(170): Show | 210 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(207): Show |
intron_variant | MODIFIER | c.798-2947C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705388 | ||||||
chr4:184705435
|
G | A | 1 | a0002c0002t0002g0061 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.798-2994C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705435 | ||||||
chr4:184705451
|
C | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-3010G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705451 | ||||||
chr4:184705488
|
A | G | 1 | a0002c0002t0002g0040 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.798-3047T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705488 | ||||||
chr4:184705579
|
T | TA | 36 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(33): Show | 47 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.798-3139dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705579 | ||||||
chr4:184705579
|
TA | T | 15 | a0004c0004t0001g0028a0004c0004t0001g0029a0004c0004t0001g0030others(12): Show | 18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.798-3139delT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705579 | ||||||
chr4:184705628
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.798-3187A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705628 | ||||||
chr4:184705874
|
T | G | 1 | a0001c0001t0007g0235 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.798-3433A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705874 | ||||||
chr4:184705978
|
G | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-3537C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705978 | ||||||
chr4:184706044
|
C | T | 18 | a0003c0008t0004g0157a0003c0008t0004g0242a0003c0008t0004g0249others(15): Show | 27 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.798-3603G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706044 | ||||||
chr4:184706108
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-3667A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706108 | ||||||
chr4:184706150
|
T | TA | 19 | a0003c0008t0004g0157a0003c0008t0004g0242a0003c0008t0004g0249others(16): Show | 28 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.798-3710dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706150 | ||||||
chr4:184706150
|
T | TAA | 21 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(18): Show | 23 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.798-3711_798-3710d others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706150 | ||||||
chr4:184706262
|
T | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+3810A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706262 | ||||||
chr4:184706327
|
C | T | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.797+3745G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706327 | ||||||
chr4:184706471
|
C | T | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0230 | 3 | NA18939.hp2 NA18977.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.797+3601G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706471 | ||||||
chr4:184706568
|
C | G | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.797+3504G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706568 | ||||||
chr4:184706592
|
A | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+3480T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706592 | ||||||
chr4:184706607
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+3465C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706607 | ||||||
chr4:184706866
|
ACTGCAGC others(504): Show |
A | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 6 | HG02056.hp1 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.797+2695_797+3205d others(2): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706866 | ||||||
chr4:184706937
|
T | C | 7 | a0006c0006t0005g0008a0006c0006t0005g0016a0006c0006t0005g0126others(4): Show | 10 | HG00639.hp2 HG00733.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.797+3135A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706937 | ||||||
chr4:184706999
|
T | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+3073A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706999 | ||||||
chr4:184707157
|
G | C | 1 | a0002c0002t0002g0041 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.797+2915C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707157 | ||||||
chr4:184707161
|
C | G | 1 | a0002c0002t0002g0110 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.797+2911G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707161 | ||||||
chr4:184707250
|
G | C | 3 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | NA18990.hp2 NA19000.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.797+2822C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707250 | ||||||
chr4:184707251
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+2821T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707251 | ||||||
chr4:184707252
|
A | G | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.797+2820T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707252 | ||||||
chr4:184707303
|
A | G | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.797+2769T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707303 | ||||||
chr4:184707480
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.797+2592C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707480 | ||||||
chr4:184707556
|
G | C | 1 | a0003c0003t0003g0245 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.797+2516C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707556 | ||||||
chr4:184707688
|
G | A | 1 | a0002c0002t0002g0112 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.797+2384C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707688 | ||||||
chr4:184707812
|
G | A | 1 | a0005c0005t0016g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.797+2260C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707812 | ||||||
chr4:184707830
|
G | C | 2 | a0001c0001t0012g0252a0001c0001t0012g0253 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.797+2242C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707830 | ||||||
chr4:184707951
|
G | A | 3 | a0001c0001t0010g0145a0001c0001t0010g0146a0001c0001t0010g0148 | 3 | HG02970.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.797+2121C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707951 | ||||||
chr4:184708015
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+2057C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708015 | ||||||
chr4:184708049
|
C | T | 4 | a0005c0007t0003g0281a0005c0007t0003g0282a0005c0007t0003g0283others(1): Show | 4 | HG02280.hp2 HG02809.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.797+2023G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708049 | ||||||
chr4:184708092
|
C | T | 7 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.797+1980G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708092 | ||||||
chr4:184708096
|
T | C | 21 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(18): Show | 23 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.797+1976A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708096 | ||||||
chr4:184708178
|
G | A | 5 | a0001c0001t0002g0151a0002c0002t0002g0074a0002c0002t0002g0076others(2): Show | 5 | HG00621.hp1 HG02165.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.797+1894C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708178 | ||||||
chr4:184708185
|
G | A | 114 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(111): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.797+1887C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708185 | ||||||
chr4:184708204
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+1868A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708204 | ||||||
chr4:184708211
|
AG | A | 6 | a0003c0003t0003g0245a0003c0003t0003g0246a0005c0007t0003g0281others(3): Show | 6 | HG02280.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.797+1860delC | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708211 | ||||||
chr4:184708212
|
G | A | 34 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0267others(31): Show | 45 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.797+1860C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708212 | ||||||
chr4:184708219
|
T | A | 103 | a0001c0001t0002g0150a0001c0001t0002g0151a0002c0002t0002g0001others(100): Show | 126 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.797+1853A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708219 | ||||||
chr4:184708222
|
CA | C | 212 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(209): Show | 255 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.797+1849delT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708222 | ||||||
chr4:184708222
|
CAA | C | 24 | a0001c0001t0001g0023a0001c0001t0001g0147a0001c0001t0001g0156others(21): Show | 25 | HG00099.hp2 HG01081.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.797+1848_797+1849d others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708222 | ||||||
chr4:184708222
|
CAAAAAAA others(6): Show |
C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+1837_797+1849d others(15): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708222 | ||||||
chr4:184708230
|
A | G | 3 | a0001c0001t0001g0183a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | HG00639.hp1 HG00738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.797+1842T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708230 | ||||||
chr4:184708252
|
T | A | 15 | a0004c0004t0001g0028a0004c0004t0001g0029a0004c0004t0001g0030others(12): Show | 18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.797+1820A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708252 | ||||||
chr4:184708480
|
A | T | 1 | a0001c0001t0017g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.797+1592T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708480 | ||||||
chr4:184708533
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.797+1539G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708533 | ||||||
chr4:184708534
|
AAAG | A | 17 | a0003c0008t0004g0157a0003c0008t0004g0242a0003c0008t0004g0249others(14): Show | 26 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.797+1535_797+1537d others(5): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708534 | ||||||
chr4:184708537
|
G | GA | 10 | a0002c0002t0002g0001a0002c0002t0002g0006a0002c0002t0002g0033others(7): Show | 18 | HG00558.hp2 HG00621.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.797+1534dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708537 | ||||||
chr4:184708614
|
C | T | 6 | a0003c0003t0003g0245a0003c0003t0003g0246a0005c0007t0003g0281others(3): Show | 6 | HG02280.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.797+1458G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708614 | ||||||
chr4:184708635
|
A | T | 103 | a0001c0001t0002g0150a0001c0001t0002g0151a0002c0002t0002g0001others(100): Show | 126 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.797+1437T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708635 | ||||||
chr4:184708651
|
C | A | 17 | a0003c0008t0004g0157a0003c0008t0004g0242a0003c0008t0004g0249others(14): Show | 26 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.797+1421G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708651 | ||||||
chr4:184708718
|
A | C | 15 | a0004c0004t0001g0028a0004c0004t0001g0029a0004c0004t0001g0030others(12): Show | 18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.797+1354T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708718 | ||||||
chr4:184708775
|
C | T | 7 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.797+1297G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708775 | ||||||
chr4:184708857
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+1215A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708857 | ||||||
chr4:184708871
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+1201C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708871 | ||||||
chr4:184709018
|
AAAAGTT | A | 61 | a0001c0001t0002g0150a0001c0001t0002g0151a0002c0002t0002g0002others(58): Show | 73 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.797+1048_797+1053d others(8): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709018 | ||||||
chr4:184709122
|
G | C | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.797+950C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709122 | ||||||
chr4:184709162
|
G | A | 2 | a0006c0006t0005g0126a0006c0006t0005g0129 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.797+910C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709162 | ||||||
chr4:184709227
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+845C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709227 | ||||||
chr4:184709348
|
G | A | 1 | a0002c0002t0002g0063 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.797+724C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709348 | ||||||
chr4:184709378
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+694A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709378 | ||||||
chr4:184709444
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+628A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709444 | ||||||
chr4:184709485
|
C | CA | 48 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(45): Show | 60 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.797+586dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709485 | ||||||
chr4:184709646
|
T | C | 1 | a0002c0002t0002g0061 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.797+426A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709646 | ||||||
chr4:184709656
|
T | C | 2 | a0002c0002t0002g0086a0002c0002t0002g0089 | 2 | NA18986.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.797+416A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709656 | ||||||
chr4:184709726
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+346A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709726 | ||||||
chr4:184709736
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+336A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709736 | ||||||
chr4:184709794
|
T | A | 3 | a0001c0001t0001g0204a0001c0001t0015g0203a0002c0002t0002g0124 | 3 | HG02630.hp1 HG02647.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.797+278A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709794 | ||||||
chr4:184709830
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.797+242A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709830 | ||||||
chr4:184709892
|
T | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0167 | 3 | NA18966.hp1 NA19075.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.797+180A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709892 | ||||||
chr4:184710010
|
G | T | 1 | a0001c0001t0010g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.797+62C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184710010 | ||||||
chr4:184710184
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
splice_region_variant&intron_variant | LOW | c.689-4T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710184 | ||||||
chr4:184710314
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.689-134A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710314 | ||||||
chr4:184710322
|
T | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0221 | 2 | NA18961.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.689-142A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710322 | ||||||
chr4:184710345
|
T | A | 1 | a0001c0001t0001g0140 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.689-165A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710345 | ||||||
chr4:184710361
|
A | C | 15 | a0004c0004t0001g0028a0004c0004t0001g0029a0004c0004t0001g0030others(12): Show | 18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.689-181T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710361 | ||||||
chr4:184710550
|
G | A | 2 | a0002c0002t0002g0090a0002c0002t0002g0106 | 2 | NA19001.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.689-370C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710550 | ||||||
chr4:184710667
|
C | CA | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.689-488_689-487ins others(1): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710667 | ||||||
chr4:184710844
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.689-664A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710844 | ||||||
chr4:184710859
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.689-679C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710859 | ||||||
chr4:184710865
|
T | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.689-685A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710865 | ||||||
chr4:184711004
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.689-824G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711004 | ||||||
chr4:184711005
|
G | A | 12 | a0001c0001t0006g0025a0001c0001t0006g0260a0001c0001t0006g0261others(9): Show | 13 | HG01884.hp2 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.689-825C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711005 | ||||||
chr4:184711010
|
T | C | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.689-830A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711010 | ||||||
chr4:184711087
|
G | GCTAACC | 7 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-908_689-907ins others(6): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711087 | ||||||
chr4:184711090
|
C | A | 7 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-910G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711090 | ||||||
chr4:184711092
|
A | C | 7 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-912T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711092 | ||||||
chr4:184711093
|
G | C | 7 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-913C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711093 | ||||||
chr4:184711095
|
A | T | 7 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-915T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711095 | ||||||
chr4:184711097
|
T | A | 7 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-917A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711097 | ||||||
chr4:184711099
|
T | C | 7 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-919A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711099 | ||||||
chr4:184711102
|
C | A | 7 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-922G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711102 | ||||||
chr4:184711131
|
C | T | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.689-951G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711131 | ||||||
chr4:184711132
|
G | A | 1 | a0004c0004t0009g0298 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.689-952C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711132 | ||||||
chr4:184711135
|
T | G | 7 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-955A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711135 | ||||||
chr4:184711273
|
T | C | 1 | a0001c0001t0017g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.689-1093A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711273 | ||||||
chr4:184711324
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.689-1144A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711324 | ||||||
chr4:184711547
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.689-1367G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711547 | ||||||
chr4:184711736
|
T | C | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.688+1208A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711736 | ||||||
chr4:184711807
|
C | T | 3 | a0001c0001t0010g0145a0001c0001t0010g0146a0001c0001t0010g0148 | 3 | HG02970.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.688+1137G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711807 | ||||||
chr4:184711811
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.688+1133G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711811 | ||||||
chr4:184711875
|
C | A | 1 | a0001c0001t0001g0161 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.688+1069G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711875 | ||||||
chr4:184712031
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.688+913C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712031 | ||||||
chr4:184712036
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.688+908C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712036 | ||||||
chr4:184712069
|
G | C | 300 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(297): Show | 355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.688+875C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712069 | ||||||
chr4:184712119
|
C | CA | 53 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0024others(50): Show | 60 | HG00099.hp1 HG00733.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.688+824dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712119 | ||||||
chr4:184712119
|
C | CAAAAA | 13 | a0003c0003t0003g0027a0003c0003t0003g0267a0003c0003t0003g0269others(10): Show | 14 | HG01081.hp1 HG01167.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.688+820_688+824dup others(5): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712119 | ||||||
chr4:184712119
|
C | CAAAAAA | 8 | a0003c0003t0003g0026a0003c0003t0003g0268a0003c0008t0004g0157others(5): Show | 12 | HG00639.hp2 HG00733.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.688+819_688+824dup others(6): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712119 | ||||||
chr4:184712119
|
C | CAAAAAAA | 14 | a0003c0003t0003g0245a0003c0003t0003g0246a0003c0008t0004g0242others(11): Show | 20 | HG00642.hp1 HG01123.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.688+818_688+824dup others(7): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712119 | ||||||
chr4:184712119
|
C | CAAAAAAA others(3): Show |
1 | a0005c0005t0016g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.688+815_688+824dup others(10): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712119 | ||||||
chr4:184712119
|
CA | C | 8 | a0001c0001t0001g0178a0001c0001t0001g0202a0001c0001t0001g0204others(5): Show | 8 | HG01891.hp1 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.688+824delT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712119 | ||||||
chr4:184712171
|
C | G | 1 | a0004c0004t0009g0298 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.688+773G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712171 | ||||||
chr4:184712310
|
T | C | 2 | a0002c0002t0011g0108a0002c0002t0011g0109 | 2 | NA18961.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.688+634A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712310 | ||||||
chr4:184712379
|
G | A | 1 | a0002c0002t0002g0111 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.688+565C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712379 | ||||||
chr4:184712392
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.688+552T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712392 | ||||||
chr4:184712427
|
G | A | 1 | a0002c0012t0007g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.688+517C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712427 | ||||||
chr4:184712711
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.688+233C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712711 | ||||||
chr4:184712919
|
C | A | 15 | a0004c0004t0001g0028a0004c0004t0001g0029a0004c0004t0001g0030others(12): Show | 18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.688+25G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712919 | ||||||
chr4:184713017
|
CA | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
splice_region_variant&intron_variant | LOW | c.619-5delT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713017 | ||||||
chr4:184713064
|
A | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.619-51T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713064 | ||||||
chr4:184713087
|
C | A | 1 | a0002c0002t0002g0099 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.619-74G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713087 | ||||||
chr4:184713219
|
C | T | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.619-206G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713219 | ||||||
chr4:184713599
|
G | A | 1 | a0002c0002t0002g0091 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.619-586C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713599 | ||||||
chr4:184713683
|
T | C | 286 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(283): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.619-670A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713683 | ||||||
chr4:184713705
|
A | T | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.619-692T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713705 | ||||||
chr4:184713714
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.619-701A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713714 | ||||||
chr4:184713722
|
A | G | 1 | a0004c0004t0009g0293 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.619-709T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713722 | ||||||
chr4:184713864
|
G | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.619-851C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713864 | ||||||
chr4:184714004
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.619-991G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714004 | ||||||
chr4:184714005
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.619-992A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714005 | ||||||
chr4:184714095
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.619-1082T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714095 | ||||||
chr4:184714157
|
C | T | 109 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(106): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.619-1144G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714157 | ||||||
chr4:184714181
|
A | G | 2 | a0002c0002t0002g0077a0002c0002t0002g0113 | 2 | HG00735.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.619-1168T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714181 | ||||||
chr4:184714210
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.619-1197T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714210 | ||||||
chr4:184714265
|
A | C | 1 | a0002c0002t0002g0076 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.619-1252T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714265 | ||||||
chr4:184714310
|
G | C | 1 | a0002c0002t0002g0104 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.619-1297C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714310 | ||||||
chr4:184714363
|
T | C | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.619-1350A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714363 | ||||||
chr4:184714427
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.619-1414C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714427 | ||||||
chr4:184714552
|
T | C | 1 | a0002c0002t0002g0110 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.619-1539A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714552 | ||||||
chr4:184714612
|
T | A | 287 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(284): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.619-1599A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714612 | ||||||
chr4:184714680
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.619-1667A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714680 | ||||||
chr4:184714868
|
A | G | 33 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0017others(30): Show | 40 | HG00280.hp2 HG00642.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.618+1529T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714868 | ||||||
chr4:184714905
|
CAGTA | C | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.618+1488_618+1491d others(6): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714905 | ||||||
chr4:184714909
|
A | G | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.618+1488T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714909 | ||||||
chr4:184714926
|
C | T | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.618+1471G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714926 | ||||||
chr4:184714942
|
G | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+1455C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714942 | ||||||
chr4:184714951
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+1446A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714951 | ||||||
chr4:184715024
|
T | C | 1 | a0001c0001t0006g0265 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.618+1373A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715024 | ||||||
chr4:184715063
|
T | A | 148 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0266others(145): Show | 182 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(179): Show |
intron_variant | MODIFIER | c.618+1334A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715063 | ||||||
chr4:184715120
|
A | C | 15 | a0004c0004t0001g0028a0004c0004t0001g0029a0004c0004t0001g0030others(12): Show | 18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.618+1277T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715120 | ||||||
chr4:184715126
|
C | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+1271G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715126 | ||||||
chr4:184715137
|
G | A | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.618+1260C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715137 | ||||||
chr4:184715242
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+1155C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715242 | ||||||
chr4:184715251
|
A | G | 1 | a0001c0001t0017g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.618+1146T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715251 | ||||||
chr4:184715305
|
G | A | 6 | a0003c0003t0003g0245a0003c0003t0003g0246a0005c0007t0003g0281others(3): Show | 6 | HG02280.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.618+1092C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715305 | ||||||
chr4:184715323
|
A | G | 1 | a0002c0002t0001g0121 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.618+1074T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715323 | ||||||
chr4:184715388
|
T | C | 8 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(5): Show | 9 | HG02056.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.618+1009A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715388 | ||||||
chr4:184715397
|
C | CA | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+999dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715397 | ||||||
chr4:184715405
|
G | A | 1 | a0002c0002t0002g0092 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.618+992C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715405 | ||||||
chr4:184715414
|
G | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+983C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715414 | ||||||
chr4:184715427
|
T | C | 3 | a0002c0002t0008g0046a0002c0002t0008g0062a0002c0002t0008g0067 | 3 | HG01952.hp1 HG02004.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.618+970A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715427 | ||||||
chr4:184715432
|
C | T | 3 | a0004c0004t0009g0296a0004c0004t0009g0297a0004c0004t0014g0295 | 3 | HG01975.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.618+965G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715432 | ||||||
chr4:184715462
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.618+935C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715462 | ||||||
chr4:184715495
|
T | C | 17 | a0003c0008t0004g0157a0003c0008t0004g0242a0003c0008t0004g0249others(14): Show | 26 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.618+902A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715495 | ||||||
chr4:184715548
|
C | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+849G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715548 | ||||||
chr4:184715609
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.618+788C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715609 | ||||||
chr4:184715654
|
G | C | 1 | a0001c0001t0001g0222 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.618+743C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715654 | ||||||
chr4:184715678
|
A | C | 15 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0267others(12): Show | 17 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.618+719T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715678 | ||||||
chr4:184715926
|
GCT | G | 15 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0267others(12): Show | 17 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.618+469_618+470del others(2): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715926 | ||||||
chr4:184715927
|
C | T | 272 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(269): Show | 324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.618+470G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715927 | ||||||
chr4:184715937
|
G | GT | 116 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0143others(113): Show | 140 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.618+459dupA | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715937 | ||||||
chr4:184715937
|
G | T | 15 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0267others(12): Show | 17 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.618+460C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715937 | ||||||
chr4:184715937
|
GTTT | G | 25 | a0003c0003t0003g0245a0003c0003t0003g0246a0003c0008t0004g0157others(22): Show | 34 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.618+457_618+459del others(3): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715937 | ||||||
chr4:184715940
|
T | G | 15 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0267others(12): Show | 17 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.618+457A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715940 | ||||||
chr4:184715941
|
T | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+456A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715941 | ||||||
chr4:184715955
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+442G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715955 | ||||||
chr4:184715994
|
G | A | 2 | a0004c0004t0009g0293a0004c0004t0009g0294 | 2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.618+403C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715994 | ||||||
chr4:184716193
|
C | T | 1 | a0002c0002t0002g0075 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.618+204G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184716193 | ||||||
chr4:184716227
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+170C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184716227 | ||||||
chr4:184716232
|
G | A | 1 | a0002c0002t0002g0104 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.618+165C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184716232 | ||||||
chr4:184716264
|
C | T | 169 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(166): Show | 206 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(203): Show |
intron_variant | MODIFIER | c.618+133G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184716264 | ||||||
chr4:184716369
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+28G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184716369 | ||||||
chr4:184716389
|
G | A | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | splice_region_variant&intron_variant | LOW | c.618+8C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184716389 | ||||||
chr4:184716727
|
T | A | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.382-94A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 5/12 | chr4 | 184716727 | ||||||
chr4:184716740
|
C | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.382-107G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 5/12 | chr4 | 184716740 | ||||||
chr4:184716750
|
T | C | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.382-117A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 5/12 | chr4 | 184716750 | ||||||
chr4:184716970
|
G | C | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.381+166C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 5/12 | chr4 | 184716970 | ||||||
chr4:184717010
|
G | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0177 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.381+126C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 5/12 | chr4 | 184717010 | ||||||
chr4:184717077
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.381+59G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 5/12 | chr4 | 184717077 | ||||||
chr4:184717126
|
T | G | 1 | a0001c0001t0010g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.381+10A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 5/12 | chr4 | 184717126 | ||||||
chr4:184717240
|
T | C | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.321-44A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717240 | ||||||
chr4:184717353
|
G | A | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.321-157C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717353 | ||||||
chr4:184717569
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-373C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717569 | ||||||
chr4:184717675
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-479A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717675 | ||||||
chr4:184717682
|
A | G | 4 | a0001c0001t0001g0175a0001c0001t0001g0183a0001c0001t0001g0185others(1): Show | 4 | HG02738.hp1 HG03239.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.321-486T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717682 | ||||||
chr4:184717699
|
G | A | 114 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(111): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.321-503C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717699 | ||||||
chr4:184717714
|
A | C | 1 | a0002c0002t0002g0101 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.321-518T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717714 | ||||||
chr4:184717722
|
C | T | 147 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0266others(144): Show | 181 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(178): Show |
intron_variant | MODIFIER | c.321-526G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717722 | ||||||
chr4:184717746
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-550C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717746 | ||||||
chr4:184717800
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-604T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717800 | ||||||
chr4:184717848
|
A | G | 107 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0266others(104): Show | 130 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.321-652T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717848 | ||||||
chr4:184717848
|
A | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-652T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717848 | ||||||
chr4:184717924
|
C | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-728G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717924 | ||||||
chr4:184717941
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-745G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717941 | ||||||
chr4:184717977
|
T | A | 1 | a0002c0002t0002g0037 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.321-781A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717977 | ||||||
chr4:184717980
|
A | G | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.321-784T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717980 | ||||||
chr4:184718015
|
G | A | 114 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(111): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.321-819C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718015 | ||||||
chr4:184718038
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-842G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718038 | ||||||
chr4:184718179
|
G | A | 1 | a0002c0002t0002g0082 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.321-983C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718179 | ||||||
chr4:184718301
|
C | T | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.321-1105G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718301 | ||||||
chr4:184718321
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1125G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718321 | ||||||
chr4:184718348
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1152A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718348 | ||||||
chr4:184718371
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1175C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718371 | ||||||
chr4:184718566
|
A | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1370T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718566 | ||||||
chr4:184718574
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1378A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718574 | ||||||
chr4:184718588
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1392C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718588 | ||||||
chr4:184718608
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1412T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718608 | ||||||
chr4:184718705
|
C | A | 1 | a0001c0001t0001g0226 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.321-1509G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718705 | ||||||
chr4:184718740
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1544T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718740 | ||||||
chr4:184718749
|
G | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1553C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718749 | ||||||
chr4:184718807
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1611G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718807 | ||||||
chr4:184718843
|
A | G | 1 | a0004c0004t0009g0298 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.321-1647T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718843 | ||||||
chr4:184718846
|
G | A | 21 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(18): Show | 23 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.321-1650C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718846 | ||||||
chr4:184718850
|
A | G | 287 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(284): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.321-1654T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718850 | ||||||
chr4:184718903
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1707G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718903 | ||||||
chr4:184718924
|
G | A | 1 | a0003c0003t0003g0246 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.321-1728C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718924 | ||||||
chr4:184719062
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1866A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719062 | ||||||
chr4:184719094
|
A | G | 2 | a0004c0004t0009g0293a0004c0004t0009g0294 | 2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.321-1898T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719094 | ||||||
chr4:184719276
|
C | T | 1 | a0001c0001t0007g0254 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.321-2080G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719276 | ||||||
chr4:184719377
|
A | G | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.321-2181T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719377 | ||||||
chr4:184719494
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-2298G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719494 | ||||||
chr4:184719530
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-2334C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719530 | ||||||
chr4:184719563
|
C | G | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.321-2367G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719563 | ||||||
chr4:184719619
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-2423T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719619 | ||||||
chr4:184719638
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-2442A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719638 | ||||||
chr4:184719658
|
T | G | 1 | a0001c0001t0001g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.321-2462A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719658 | ||||||
chr4:184719686
|
C | G | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.321-2490G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719686 | ||||||
chr4:184719798
|
C | G | 1 | a0001c0001t0001g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.321-2602G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719798 | ||||||
chr4:184719798
|
C | T | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.321-2602G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719798 | ||||||
chr4:184719931
|
A | G | 3 | a0001c0001t0010g0145a0001c0001t0010g0146a0001c0001t0010g0148 | 3 | HG02970.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.321-2735T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719931 | ||||||
chr4:184719971
|
C | T | 7 | a0006c0006t0005g0008a0006c0006t0005g0016a0006c0006t0005g0126others(4): Show | 10 | HG00639.hp2 HG00733.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.321-2775G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719971 | ||||||
chr4:184720172
|
TTAAC | T | 18 | a0003c0008t0004g0157a0003c0008t0004g0242a0003c0008t0004g0249others(15): Show | 27 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.321-2980_321-2977d others(6): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720172 | ||||||
chr4:184720229
|
G | T | 1 | a0004c0004t0009g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.321-3033C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720229 | ||||||
chr4:184720236
|
A | G | 1 | a0004c0004t0009g0298 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.321-3040T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720236 | ||||||
chr4:184720343
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-3147C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720343 | ||||||
chr4:184720383
|
G | T | 15 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0162others(12): Show | 18 | HG02015.hp2 HG02083.hp2 HG03831.hp2 others(15): Show |
intron_variant | MODIFIER | c.321-3187C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720383 | ||||||
chr4:184720402
|
A | T | 3 | a0002c0002t0002g0012a0002c0002t0002g0057a0002c0002t0002g0065 | 4 | HG01243.hp2 HG01257.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.321-3206T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720402 | ||||||
chr4:184720414
|
G | A | 51 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0017others(48): Show | 59 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.321-3218C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720414 | ||||||
chr4:184720474
|
G | A | 3 | a0001c0001t0002g0266a0001c0001t0012g0252a0001c0001t0012g0253 | 3 | HG03209.hp1 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.321-3278C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720474 | ||||||
chr4:184720557
|
T | C | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.321-3361A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720557 | ||||||
chr4:184720844
|
T | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-3648A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720844 | ||||||
chr4:184721020
|
T | C | 107 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0266others(104): Show | 130 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.321-3824A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721020 | ||||||
chr4:184721181
|
T | C | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.320+3776A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721181 | ||||||
chr4:184721227
|
T | C | 7 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0234others(4): Show | 7 | HG00639.hp1 HG00738.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.320+3730A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721227 | ||||||
chr4:184721245
|
A | C | 1 | a0001c0001t0001g0134 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.320+3712T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721245 | ||||||
chr4:184721423
|
C | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+3534G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721423 | ||||||
chr4:184721457
|
T | TAA | 106 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(103): Show | 121 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.320+3498_320+3499d others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721457 | ||||||
chr4:184721457
|
T | TAAA | 111 | a0001c0001t0001g0020a0001c0001t0001g0138a0001c0001t0001g0140others(108): Show | 138 | HG00558.hp1 HG00558.hp2 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.320+3497_320+3499d others(5): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721457 | ||||||
chr4:184721457
|
T | TAAAA | 25 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(22): Show | 26 | HG00280.hp1 HG00609.hp2 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.320+3496_320+3499d others(6): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721457 | ||||||
chr4:184721457
|
T | TAAAAAAA others(1): Show |
14 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0267others(11): Show | 16 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.320+3492_320+3499d others(10): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721457 | ||||||
chr4:184721478
|
AG | A | 16 | a0003c0008t0004g0157a0003c0008t0004g0242a0003c0008t0004g0249others(13): Show | 25 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.320+3478delC | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721478 | ||||||
chr4:184721479
|
G | A | 20 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(17): Show | 22 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.320+3478C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721479 | ||||||
chr4:184721554
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.320+3403C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721554 | ||||||
chr4:184721614
|
G | C | 10 | a0003c0008t0004g0157a0003c0008t0004g0242a0003c0008t0004g0249others(7): Show | 16 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.320+3343C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721614 | ||||||
chr4:184721620
|
CTAGATT | C | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.320+3331_320+3336d others(8): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721620 | ||||||
chr4:184721711
|
G | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+3246C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721711 | ||||||
chr4:184721715
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+3242G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721715 | ||||||
chr4:184721740
|
C | A | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.320+3217G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721740 | ||||||
chr4:184721789
|
A | G | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.320+3168T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721789 | ||||||
chr4:184721806
|
T | G | 1 | a0002c0002t0002g0086 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.320+3151A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721806 | ||||||
chr4:184721848
|
A | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+3109T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721848 | ||||||
chr4:184721934
|
G | T | 287 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(284): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.320+3023C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721934 | ||||||
chr4:184721957
|
C | A | 8 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(5): Show | 9 | HG02056.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.320+3000G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721957 | ||||||
chr4:184721988
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.320+2969G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721988 | ||||||
chr4:184722007
|
A | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+2950T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722007 | ||||||
chr4:184722015
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.320+2942T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722015 | ||||||
chr4:184722069
|
T | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+2888A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722069 | ||||||
chr4:184722099
|
T | C | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.320+2858A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722099 | ||||||
chr4:184722131
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.320+2826A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722131 | ||||||
chr4:184722182
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+2775G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722182 | ||||||
chr4:184722417
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+2540A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722417 | ||||||
chr4:184722542
|
C | T | 1 | a0002c0002t0002g0086 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.320+2415G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722542 | ||||||
chr4:184722543
|
G | A | 1 | a0001c0001t0006g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.320+2414C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722543 | ||||||
chr4:184722588
|
G | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+2369C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722588 | ||||||
chr4:184722621
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+2336C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722621 | ||||||
chr4:184722624
|
C | G | 1 | a0003c0003t0003g0245 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.320+2333G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722624 | ||||||
chr4:184722670
|
CAA | C | 3 | a0002c0002t0002g0007a0002c0002t0002g0054a0002c0002t0002g0064 | 5 | HG01256.hp2 HG01258.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.320+2285_320+2286d others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722670 | ||||||
chr4:184722703
|
A | G | 1 | a0005c0005t0016g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.320+2254T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722703 | ||||||
chr4:184722708
|
A | G | 38 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(35): Show | 49 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.320+2249T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722708 | ||||||
chr4:184722718
|
A | AAC | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.320+2238_320+2239i others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722718 | ||||||
chr4:184722724
|
A | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0142others(3): Show | 6 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.320+2233T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722724 | ||||||
chr4:184722791
|
A | G | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.320+2166T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722791 | ||||||
chr4:184722797
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.320+2160A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722797 | ||||||
chr4:184722822
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.320+2135G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722822 | ||||||
chr4:184722830
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+2127C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722830 | ||||||
chr4:184722830
|
G | C | 15 | a0004c0004t0001g0028a0004c0004t0001g0029a0004c0004t0001g0030others(12): Show | 18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.320+2127C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722830 | ||||||
chr4:184722863
|
A | G | 1 | a0001c0001t0012g0252 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.320+2094T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722863 | ||||||
chr4:184722989
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+1968C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722989 | ||||||
chr4:184723237
|
G | A | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.320+1720C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723237 | ||||||
chr4:184723263
|
G | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+1694C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723263 | ||||||
chr4:184723339
|
TTAA | T | 7 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.320+1615_320+1617d others(5): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723339 | ||||||
chr4:184723363
|
T | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+1594A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723363 | ||||||
chr4:184723425
|
T | C | 3 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | NA18973.hp1 NA18979.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.320+1532A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723425 | ||||||
chr4:184723507
|
C | CAT | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+1449_320+1450i others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723507 | ||||||
chr4:184723579
|
A | C | 1 | a0001c0001t0001g0184 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.320+1378T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723579 | ||||||
chr4:184723615
|
G | A | 107 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0266others(104): Show | 130 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.320+1342C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723615 | ||||||
chr4:184723659
|
T | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+1298A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723659 | ||||||
chr4:184723676
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.320+1281A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723676 | ||||||
chr4:184723735
|
C | T | 1 | a0002c0012t0007g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.320+1222G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723735 | ||||||
chr4:184723756
|
T | C | 1 | a0001c0001t0017g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.320+1201A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723756 | ||||||
chr4:184723772
|
G | A | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.320+1185C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723772 | ||||||
chr4:184723775
|
G | A | 1 | a0001c0001t0006g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.320+1182C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723775 | ||||||
chr4:184723782
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+1175T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723782 | ||||||
chr4:184723841
|
CA | C | 93 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(90): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.320+1115delT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723841 | ||||||
chr4:184723841
|
CAA | C | 190 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0023others(187): Show | 232 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(229): Show |
intron_variant | MODIFIER | c.320+1114_320+1115d others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723841 | ||||||
chr4:184723841
|
CAAA | C | 12 | a0001c0001t0006g0264a0002c0002t0002g0038a0002c0002t0002g0073others(9): Show | 12 | HG01975.hp2 HG02165.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.320+1113_320+1115d others(5): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723841 | ||||||
chr4:184723857
|
A | T | 4 | a0001c0001t0001g0153a0001c0001t0001g0213a0001c0001t0001g0214others(1): Show | 4 | HG01515.hp1 HG01517.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.320+1100T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723857 | ||||||
chr4:184723930
|
T | C | 1 | a0002c0002t0002g0098 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.320+1027A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723930 | ||||||
chr4:184723958
|
A | G | 15 | a0004c0004t0001g0028a0004c0004t0001g0029a0004c0004t0001g0030others(12): Show | 18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.320+999T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723958 | ||||||
chr4:184724040
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+917T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724040 | ||||||
chr4:184724050
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+907T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724050 | ||||||
chr4:184724061
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+896C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724061 | ||||||
chr4:184724069
|
C | G | 4 | a0001c0001t0001g0280a0001c0001t0010g0145a0001c0001t0010g0146others(1): Show | 4 | HG02970.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.320+888G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724069 | ||||||
chr4:184724071
|
T | C | 21 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(18): Show | 23 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.320+886A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724071 | ||||||
chr4:184724080
|
T | C | 1 | a0003c0003t0003g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.320+877A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724080 | ||||||
chr4:184724118
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+839G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724118 | ||||||
chr4:184724134
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.320+823G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724134 | ||||||
chr4:184724138
|
C | T | 18 | a0003c0008t0004g0157a0003c0008t0004g0242a0003c0008t0004g0249others(15): Show | 27 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.320+819G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724138 | ||||||
chr4:184724148
|
C | T | 107 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0266others(104): Show | 130 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.320+809G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724148 | ||||||
chr4:184724173
|
G | C | 12 | a0001c0001t0006g0025a0001c0001t0006g0260a0001c0001t0006g0261others(9): Show | 13 | HG01884.hp2 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.320+784C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724173 | ||||||
chr4:184724265
|
C | CA | 12 | a0001c0001t0006g0025a0001c0001t0006g0260a0001c0001t0006g0261others(9): Show | 13 | HG01884.hp2 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.320+691dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724265 | ||||||
chr4:184724284
|
A | C | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.320+673T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724284 | ||||||
chr4:184724356
|
C | T | 1 | a0002c0002t0002g0072 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.320+601G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724356 | ||||||
chr4:184724390
|
G | GATA | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+564_320+566dup others(3): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724390 | ||||||
chr4:184724418
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+539G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724418 | ||||||
chr4:184724629
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+328A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724629 | ||||||
chr4:184724681
|
A | C | 3 | a0004c0004t0009g0296a0004c0004t0009g0297a0004c0004t0014g0295 | 3 | HG01975.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.320+276T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724681 | ||||||
chr4:184724789
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.320+168G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724789 | ||||||
chr4:184725214
|
T | A | 1 | a0001c0001t0001g0167 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.215-152A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725214 | ||||||
chr4:184725322
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-260G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725322 | ||||||
chr4:184725329
|
A | G | 1 | a0001c0001t0006g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.215-267T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725329 | ||||||
chr4:184725351
|
C | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-289G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725351 | ||||||
chr4:184725409
|
G | A | 1 | a0002c0002t0008g0067 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.215-347C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725409 | ||||||
chr4:184725421
|
T | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | NA18969.hp2 NA19057.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.215-359A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725421 | ||||||
chr4:184725624
|
C | T | 3 | a0001c0001t0010g0145a0001c0001t0010g0146a0001c0001t0010g0148 | 3 | HG02970.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.215-562G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725624 | ||||||
chr4:184725766
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-704G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725766 | ||||||
chr4:184725808
|
T | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-746A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725808 | ||||||
chr4:184725953
|
G | C | 106 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0007g0235others(103): Show | 129 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.215-891C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725953 | ||||||
chr4:184725963
|
C | T | 1 | a0002c0002t0002g0051 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.215-901G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725963 | ||||||
chr4:184726064
|
T | G | 1 | a0002c0012t0007g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.215-1002A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726064 | ||||||
chr4:184726085
|
T | C | 1 | a0001c0001t0007g0258 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.215-1023A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726085 | ||||||
chr4:184726146
|
C | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-1084G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726146 | ||||||
chr4:184726191
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-1129C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726191 | ||||||
chr4:184726241
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-1179G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726241 | ||||||
chr4:184726260
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-1198T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726260 | ||||||
chr4:184726371
|
G | GA | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.215-1310dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726371 | ||||||
chr4:184726441
|
T | C | 7 | a0006c0006t0005g0008a0006c0006t0005g0016a0006c0006t0005g0126others(4): Show | 10 | HG00639.hp2 HG00733.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-1379A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726441 | ||||||
chr4:184726484
|
A | C | 5 | a0001c0001t0001g0183a0005c0007t0003g0281a0005c0007t0003g0282others(2): Show | 5 | HG02280.hp2 HG02809.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-1422T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726484 | ||||||
chr4:184726499
|
G | C | 1 | a0005c0005t0016g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.215-1437C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726499 | ||||||
chr4:184726544
|
G | GCTGGTGG others(7): Show |
1 | a0001c0001t0001g0195 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.215-1496_215-1483d others(16): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726544 | ||||||
chr4:184726577
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-1515T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726577 | ||||||
chr4:184726696
|
A | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-1634T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726696 | ||||||
chr4:184726748
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-1686C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726748 | ||||||
chr4:184726753
|
TAA | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-1693_215-1692d others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726753 | ||||||
chr4:184726861
|
G | A | 107 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0266others(104): Show | 130 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.215-1799C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726861 | ||||||
chr4:184726921
|
G | A | 2 | a0002c0002t0002g0085a0002c0002t0002g0099 | 2 | NA18970.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.215-1859C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726921 | ||||||
chr4:184726974
|
T | TG | 52 | a0001c0001t0001g0141a0001c0001t0001g0251a0001c0001t0001g0256others(49): Show | 68 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.215-1913dupC | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726974 | ||||||
chr4:184726974
|
T | TGG | 15 | a0001c0001t0001g0143a0001c0001t0006g0025a0001c0001t0006g0263others(12): Show | 19 | HG00558.hp1 HG00738.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.215-1914_215-1913d others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726974 | ||||||
chr4:184726974
|
TG | T | 119 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(116): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.215-1913delC | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726974 | ||||||
chr4:184726974
|
TGGGGG | T | 38 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(35): Show | 49 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.215-1917_215-1913d others(7): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726974 | ||||||
chr4:184726978
|
G | A | 1 | a0001c0001t0017g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.215-1916C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726978 | ||||||
chr4:184726980
|
G | T | 15 | a0004c0004t0001g0028a0004c0004t0001g0029a0004c0004t0001g0030others(12): Show | 18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.215-1918C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726980 | ||||||
chr4:184726983
|
G | T | 113 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(110): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.215-1921C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726983 | ||||||
chr4:184726988
|
G | A | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.215-1926C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726988 | ||||||
chr4:184727007
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.214+1911G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727007 | ||||||
chr4:184727041
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1877T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727041 | ||||||
chr4:184727047
|
T | C | 107 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0266others(104): Show | 130 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.214+1871A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727047 | ||||||
chr4:184727048
|
G | A | 1 | a0002c0002t0002g0098 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.214+1870C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727048 | ||||||
chr4:184727116
|
C | CA | 9 | a0001c0001t0001g0212a0001c0001t0010g0145a0001c0001t0010g0146others(6): Show | 9 | HG01975.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.214+1801dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727116 | ||||||
chr4:184727116
|
C | CAAAAAAA | 20 | a0003c0003t0003g0245a0003c0003t0003g0246a0003c0008t0004g0157others(17): Show | 29 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.214+1795_214+1801d others(9): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727116 | ||||||
chr4:184727116
|
C | CAAAAAAA others(1): Show |
15 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0267others(12): Show | 17 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.214+1794_214+1801d others(10): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727116 | ||||||
chr4:184727117
|
A | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0170a0001c0001t0001g0171others(2): Show | 7 | NA18965.hp2 NA18981.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+1801T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727117 | ||||||
chr4:184727121
|
A | G | 2 | a0001c0001t0002g0150a0002c0002t0002g0037 | 2 | NA19074.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.214+1797T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727121 | ||||||
chr4:184727335
|
A | G | 107 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0266others(104): Show | 130 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.214+1583T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727335 | ||||||
chr4:184727356
|
G | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1562C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727356 | ||||||
chr4:184727424
|
T | C | 1 | a0001c0001t0001g0231 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.214+1494A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727424 | ||||||
chr4:184727456
|
A | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1462T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727456 | ||||||
chr4:184727457
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1461A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727457 | ||||||
chr4:184727560
|
T | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1358A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727560 | ||||||
chr4:184727714
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1204A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727714 | ||||||
chr4:184727723
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1195G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727723 | ||||||
chr4:184727817
|
A | G | 2 | a0005c0005t0016g0286a0010c0013t0005g0125 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.214+1101T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727817 | ||||||
chr4:184727823
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1095G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727823 | ||||||
chr4:184727843
|
G | A | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1075C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727843 | ||||||
chr4:184727844
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1074A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727844 | ||||||
chr4:184727975
|
G | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | NA19000.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.214+943C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727975 | ||||||
chr4:184727987
|
G | C | 1 | a0001c0001t0001g0188 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.214+931C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727987 | ||||||
chr4:184728071
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.214+847G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728071 | ||||||
chr4:184728150
|
T | G | 1 | a0001c0001t0001g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.214+768A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728150 | ||||||
chr4:184728256
|
T | C | 16 | a0001c0001t0007g0235a0002c0002t0002g0013a0002c0002t0002g0014others(13): Show | 18 | HG00609.hp2 HG00738.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.214+662A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728256 | ||||||
chr4:184728277
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+641T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728277 | ||||||
chr4:184728305
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+613T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728305 | ||||||
chr4:184728335
|
T | C | 1 | a0001c0001t0017g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.214+583A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728335 | ||||||
chr4:184728376
|
A | G | 300 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(297): Show | 355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.214+542T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728376 | ||||||
chr4:184728397
|
A | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+521T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728397 | ||||||
chr4:184728507
|
G | T | 19 | a0003c0008t0004g0157a0003c0008t0004g0242a0003c0008t0004g0249others(16): Show | 28 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.214+411C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728507 | ||||||
chr4:184728673
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+245G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728673 | ||||||
chr4:184728698
|
T | C | 300 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(297): Show | 355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.214+220A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728698 | ||||||
chr4:184728712
|
C | A | 148 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0266others(145): Show | 182 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(179): Show |
intron_variant | MODIFIER | c.214+206G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728712 | ||||||
chr4:184728724
|
T | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+194A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728724 | ||||||
chr4:184728841
|
A | C | 1 | a0001c0001t0017g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.214+77T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728841 | ||||||
chr4:184729122
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.97-87G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184729122 | ||||||
chr4:184729239
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.97-204A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184729239 | ||||||
chr4:184729304
|
A | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.97-269T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184729304 | ||||||
chr4:184729667
|
A | C | 107 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0266others(104): Show | 130 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.97-632T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184729667 | ||||||
chr4:184729695
|
T | C | 4 | a0005c0007t0003g0281a0005c0007t0003g0282a0005c0007t0003g0283others(1): Show | 4 | HG02280.hp2 HG02809.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-660A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184729695 | ||||||
chr4:184729741
|
T | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.97-706A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184729741 | ||||||
chr4:184729787
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.97-752T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184729787 | ||||||
chr4:184729902
|
T | C | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.97-867A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184729902 | ||||||
chr4:184730074
|
C | A | 1 | a0002c0002t0008g0067 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.96+846G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730074 | ||||||
chr4:184730109
|
G | A | 5 | a0004c0004t0001g0028a0004c0004t0001g0291a0004c0004t0001g0292others(2): Show | 6 | HG00733.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+811C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730109 | ||||||
chr4:184730248
|
C | T | 3 | a0001c0001t0001g0201a0001c0001t0001g0211a0001c0001t0001g0212 | 3 | NA18962.hp1 NA19001.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.96+672G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730248 | ||||||
chr4:184730262
|
C | T | 39 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(36): Show | 50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.96+658G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730262 | ||||||
chr4:184730297
|
G | T | 65 | a0001c0001t0002g0150a0001c0001t0002g0151a0002c0002t0002g0002others(62): Show | 77 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.96+623C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730297 | ||||||
chr4:184730463
|
A | G | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.96+457T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730463 | ||||||
chr4:184730484
|
C | T | 40 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(37): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.96+436G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730484 | ||||||
chr4:184730505
|
G | A | 1 | a0001c0001t0017g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.96+415C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730505 | ||||||
chr4:184730507
|
T | TAAAGAAA others(314): Show |
1 | a0003c0003t0003g0246 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.96+412_96+413insTT others(319): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | ||||||
chr4:184730507
|
T | TAAAGAAA others(318): Show |
10 | a0003c0008t0004g0157a0003c0008t0004g0242a0003c0008t0004g0249others(7): Show | 16 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.96+412_96+413insTT others(323): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | ||||||
chr4:184730507
|
T | TAAAGAAA others(322): Show |
2 | a0003c0003t0003g0267a0005c0007t0003g0281 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.96+412_96+413insTT others(327): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | ||||||
chr4:184730507
|
T | TAAAGAAA others(325): Show |
7 | a0003c0003t0003g0026a0003c0003t0003g0268a0005c0007t0003g0282others(4): Show | 11 | HG00639.hp2 HG00733.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.96+412_96+413insTT others(330): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | ||||||
chr4:184730507
|
T | TAAAGAAA others(326): Show |
1 | a0006c0006t0005g0128 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.96+412_96+413insTT others(331): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | ||||||
chr4:184730507
|
T | TAAAGAAA others(328): Show |
2 | a0006c0006t0005g0126a0006c0006t0005g0129 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.96+412_96+413insTT others(333): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | ||||||
chr4:184730507
|
T | TAAAGAAA others(334): Show |
1 | a0003c0003t0003g0245 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.96+412_96+413insTT others(339): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | ||||||
chr4:184730507
|
T | TAAAGAAA others(338): Show |
2 | a0003c0003t0003g0027a0005c0007t0003g0283 | 3 | HG02280.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.96+412_96+413insTT others(343): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | ||||||
chr4:184730507
|
T | TAAAGAAA others(339): Show |
2 | a0003c0003t0003g0269a0005c0007t0003g0284 | 2 | HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.96+412_96+413insTT others(344): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | ||||||
chr4:184730507
|
T | TAAAGAAA others(343): Show |
1 | a0003c0003t0003g0270 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.96+412_96+413insTT others(348): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | ||||||
chr4:184730507
|
T | TAAAGAAA others(344): Show |
3 | a0003c0003t0003g0271a0003c0003t0003g0272a0003c0003t0003g0273 | 3 | HG01167.hp1 NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.96+412_96+413insTT others(349): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | ||||||
chr4:184730507
|
T | TAAAGAAA others(346): Show |
1 | a0003c0003t0003g0274 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.96+412_96+413insTT others(351): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | ||||||
chr4:184730507
|
T | TAAAGAAA others(351): Show |
1 | a0003c0003t0003g0275 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.96+412_96+413insTT others(356): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | ||||||
chr4:184730507
|
T | TAAAGAAA others(353): Show |
1 | a0003c0003t0003g0276 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.96+412_96+413insTT others(358): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | ||||||
chr4:184730507
|
T | TAAAGAAA others(355): Show |
2 | a0003c0003t0003g0277a0003c0003t0003g0278 | 2 | HG01081.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.96+412_96+413insTT others(360): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | ||||||
chr4:184730507
|
T | TAAAGAAA others(360): Show |
1 | a0003c0003t0003g0279 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96+412_96+413insTT others(365): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | ||||||
chr4:184730518
|
A | ACATGCGG others(322): Show |
1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.96+401_96+402insCG others(327): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730518 | ||||||
chr4:184730518
|
A | ACATGCGG others(323): Show |
1 | a0005c0005t0016g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.96+401_96+402insCG others(328): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730518 | ||||||
chr4:184730590
|
T | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG02083.hp2 NA18939.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.96+330A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730590 | ||||||
chr4:184730601
|
TA | T | 247 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(244): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.96+318delT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730601 | ||||||
chr4:184730602
|
A | C | 2 | a0005c0005t0016g0286a0010c0013t0005g0125 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.96+318T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730602 | ||||||
chr4:184730993
|
G | A | 115 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(112): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.48-25C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184730993 | ||||||
chr4:184731047
|
G | A | 247 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(244): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.48-79C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731047 | ||||||
chr4:184731070
|
AC | A | 242 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(239): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.48-103delG | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731070 | ||||||
chr4:184731071
|
C | A | 3 | a0001c0001t0017g0149a0002c0002t0002g0107a0010c0013t0005g0125 | 3 | HG02615.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.48-103G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731071 | ||||||
chr4:184731148
|
C | G | 1 | a0001c0001t0001g0189 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.48-180G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731148 | ||||||
chr4:184731195
|
G | A | 3 | a0002c0002t0002g0110a0002c0002t0011g0108a0002c0002t0011g0109 | 3 | NA18961.hp2 NA19066.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.48-227C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731195 | ||||||
chr4:184731234
|
C | G | 247 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(244): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.48-266G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731234 | ||||||
chr4:184731305
|
C | T | 1 | a0002c0002t0002g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.48-337G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731305 | ||||||
chr4:184731400
|
G | A | 21 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0245others(18): Show | 23 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.48-432C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731400 | ||||||
chr4:184731540
|
G | A | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.48-572C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731540 | ||||||
chr4:184731554
|
A | T | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.48-586T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731554 | ||||||
chr4:184731590
|
A | G | 1 | a0002c0002t0002g0119 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.48-622T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731590 | ||||||
chr4:184731594
|
C | T | 1 | a0010c0013t0005g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.48-626G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731594 | ||||||
chr4:184731673
|
C | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0243a0001c0001t0001g0244 | 4 | HG00099.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-705G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731673 | ||||||
chr4:184731676
|
G | C | 247 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(244): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.48-708C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731676 | ||||||
chr4:184731677
|
G | A | 1 | a0002c0002t0002g0111 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.48-709C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731677 | ||||||
chr4:184731717
|
A | T | 138 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(135): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.48-749T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731717 | ||||||
chr4:184731761
|
C | T | 247 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(244): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.48-793G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731761 | ||||||
chr4:184731813
|
T | A | 1 | a0001c0001t0017g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.48-845A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731813 | ||||||
chr4:184731820
|
A | G | 103 | a0001c0001t0002g0150a0001c0001t0002g0151a0002c0002t0002g0001others(100): Show | 126 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.48-852T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731820 | ||||||
chr4:184731838
|
C | G | 247 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(244): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.48-870G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731838 | ||||||
chr4:184731847
|
C | T | 287 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(284): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.48-879G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731847 | ||||||
chr4:184731881
|
C | CTGTGTGT others(9): Show |
2 | a0001c0001t0001g0159a0001c0001t0017g0149 | 2 | HG02896.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.48-914_48-913insCA others(14): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731881 | ||||||
chr4:184731883
|
C | CTG | 29 | a0001c0001t0001g0232a0001c0001t0001g0241a0001c0001t0007g0254others(26): Show | 33 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.48-917_48-916dupCA | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | ||||||
chr4:184731883
|
C | CTGTGTGT others(1): Show |
4 | a0001c0001t0010g0145a0001c0001t0010g0146a0001c0001t0010g0148others(1): Show | 4 | HG02970.hp2 HG03130.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-923_48-916dupCA others(6): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | ||||||
chr4:184731883
|
C | CTGTGTGT others(3): Show |
44 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0024others(41): Show | 50 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.48-925_48-916dupCA others(8): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | ||||||
chr4:184731883
|
C | CTGTGTGT others(5): Show |
70 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0201others(67): Show | 84 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.48-927_48-916dupCA others(10): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | ||||||
chr4:184731883
|
C | CTGTGTGT others(7): Show |
45 | a0001c0001t0001g0020a0001c0001t0001g0142a0001c0001t0001g0143others(42): Show | 58 | HG00558.hp2 HG00673.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.48-929_48-916dupCA others(12): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | ||||||
chr4:184731883
|
C | CTGTGTGT others(9): Show |
35 | a0001c0001t0001g0010a0001c0001t0001g0138a0001c0001t0001g0140others(32): Show | 40 | HG00621.hp2 HG00733.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.48-931_48-916dupCA others(14): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | ||||||
chr4:184731883
|
C | CTGTGTGT others(11): Show |
16 | a0001c0001t0001g0019a0001c0001t0001g0158a0001c0001t0001g0182others(13): Show | 17 | HG00639.hp1 HG00642.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.48-933_48-916dupCA others(16): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | ||||||
chr4:184731883
|
C | CTGTGTGT others(13): Show |
15 | a0001c0001t0001g0009a0001c0001t0001g0170a0001c0001t0001g0171others(12): Show | 17 | HG00738.hp1 HG02015.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.48-935_48-916dupCA others(18): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | ||||||
chr4:184731883
|
C | CTGTGTGT others(15): Show |
13 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0163others(10): Show | 15 | HG01168.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.48-937_48-916dupCA others(20): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | ||||||
chr4:184731883
|
C | CTGTGTGT others(17): Show |
2 | a0001c0001t0001g0162a0004c0004t0014g0295 | 2 | HG01975.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.48-939_48-916dupCA others(22): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | ||||||
chr4:184731883
|
C | CTGTGTGT others(19): Show |
2 | a0004c0004t0009g0293a0004c0004t0009g0294 | 2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.48-941_48-916dupCA others(24): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | ||||||
chr4:184731883
|
C | G | 3 | a0001c0001t0001g0159a0001c0001t0001g0233a0001c0001t0017g0149 | 3 | HG02572.hp1 HG02896.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.48-915G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | ||||||
chr4:184731904
|
T | TGC | 7 | a0001c0001t0006g0025a0001c0001t0006g0260a0001c0001t0006g0261others(4): Show | 8 | HG02280.hp1 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.48-937_48-936insGC | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731904 | ||||||
chr4:184731966
|
G | A | 1 | a0002c0002t0002g0120 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.48-998C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731966 | ||||||
chr4:184732074
|
T | C | 1 | a0001c0001t0007g0235 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.48-1106A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732074 | ||||||
chr4:184732107
|
A | G | 1 | a0003c0003t0003g0245 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.48-1139T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732107 | ||||||
chr4:184732197
|
T | A | 247 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(244): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.48-1229A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732197 | ||||||
chr4:184732222
|
A | G | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 6 | HG02056.hp1 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.48-1254T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732222 | ||||||
chr4:184732248
|
T | TA | 246 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(243): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.48-1281dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732248 | ||||||
chr4:184732366
|
C | G | 1 | a0001c0001t0001g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.48-1398G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732366 | ||||||
chr4:184732414
|
C | T | 242 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(239): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.48-1446G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732414 | ||||||
chr4:184732486
|
G | T | 1 | a0001c0001t0001g0156 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.48-1518C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732486 | ||||||
chr4:184732542
|
G | A | 249 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(246): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.47+1474C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732542 | ||||||
chr4:184732568
|
G | A | 2 | a0005c0007t0003g0283a0005c0007t0003g0284 | 2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.47+1448C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732568 | ||||||
chr4:184732611
|
C | T | 2 | a0002c0002t0002g0036a0002c0002t0008g0032 | 2 | HG02071.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.47+1405G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732611 | ||||||
chr4:184732618
|
T | TG | 120 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(117): Show | 137 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.47+1397dupC | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732618 | ||||||
chr4:184732618
|
TG | T | 15 | a0003c0008t0004g0249a0005c0005t0004g0003a0005c0005t0004g0285others(12): Show | 24 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.47+1397delC | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732618 | ||||||
chr4:184732655
|
C | G | 250 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(247): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.47+1361G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732655 | ||||||
chr4:184732672
|
G | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.47+1344C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732672 | ||||||
chr4:184732770
|
C | G | 300 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(297): Show | 355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.47+1246G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732770 | ||||||
chr4:184732919
|
T | C | 7 | a0006c0006t0005g0008a0006c0006t0005g0016a0006c0006t0005g0126others(4): Show | 10 | HG00639.hp2 HG00733.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.47+1097A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732919 | ||||||
chr4:184732985
|
C | CA | 11 | a0001c0001t0006g0025a0001c0001t0006g0260a0001c0001t0006g0261others(8): Show | 12 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.47+1030dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732985 | ||||||
chr4:184732985
|
CAA | C | 123 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(120): Show | 147 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.47+1029_47+1030del others(2): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732985 | ||||||
chr4:184732985
|
CAAA | C | 140 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(137): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.47+1028_47+1030del others(3): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732985 | ||||||
chr4:184732985
|
CAAAA | C | 12 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(9): Show | 18 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.47+1027_47+1030del others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732985 | ||||||
chr4:184733046
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T | C | 1 | a0005c0005t0004g0290 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.47+970A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733046 | ||||||
chr4:184733083
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A | G | 1 | a0001c0001t0001g0243 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.47+933T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733083 | ||||||
chr4:184733147
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C | G | 1 | a0001c0001t0001g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.47+869G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733147 | ||||||
chr4:184733166
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C | T | 115 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(112): Show | 138 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.47+850G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733166 | ||||||
chr4:184733220
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A | G | 286 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(283): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.47+796T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733220 | ||||||
chr4:184733359
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G | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0243a0001c0001t0001g0244 | 4 | HG00099.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.47+657C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733359 | ||||||
chr4:184733497
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T | C | 15 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0003g0267others(12): Show | 17 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.47+519A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733497 | ||||||
chr4:184733511
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A | C | 4 | a0001c0001t0001g0147a0001c0001t0010g0145a0001c0001t0010g0146others(1): Show | 4 | HG02486.hp2 HG02970.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+505T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733511 | ||||||
chr4:184733513
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A | C | 165 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(162): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.47+503T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733513 | ||||||
chr4:184733522
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G | C | 301 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(298): Show | 356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.47+494C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733522 | ||||||
chr4:184733529
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T | C | 137 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(134): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.47+487A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733529 | ||||||
chr4:184733556
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C | T | 7 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.47+460G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733556 | ||||||
chr4:184733569
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T | C | 170 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(167): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.47+447A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733569 | ||||||
chr4:184733598
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A | T | 1 | a0001c0001t0001g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.47+418T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733598 | ||||||
chr4:184733643
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G | A | 19 | a0004c0004t0001g0028a0004c0004t0001g0029a0004c0004t0001g0030others(16): Show | 22 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.47+373C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733643 | ||||||
chr4:184733661
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A | G | 7 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.47+355T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733661 | ||||||
chr4:184733673
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T | G | 15 | a0003c0008t0004g0249a0005c0005t0004g0003a0005c0005t0004g0285others(12): Show | 24 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.47+343A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733673 | ||||||
chr4:184733683
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C | T | 147 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(144): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.47+333G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733683 | ||||||
chr4:184733802
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C | T | 5 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(2): Show | 5 | HG01928.hp1 HG01952.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.47+214G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733802 | ||||||
chr4:184733804
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C | T | 1 | a0005c0005t0004g0285 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.47+212G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733804 | ||||||
chr4:184733937
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G | A | 1 | a0001c0001t0001g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.47+79C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733937 | ||||||
chr4:184733985
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C | G | 4 | a0005c0007t0003g0281a0005c0007t0003g0282a0005c0007t0003g0283others(1): Show | 4 | HG02280.hp2 HG02809.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.47+31G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733985 |