geneid | 9662 |
---|---|
ensemblid | ENSG00000174799.12 |
hgncid | 29086 |
symbol | CEP135 |
name | centrosomal protein 135 |
refseq_nuc | NM_025009.5 |
refseq_prot | NP_079285.2 |
ensembl_nuc | ENST00000257287.5 |
ensembl_prot | ENSP00000257287.3 |
mane_status | MANE Select |
chr | chr4 |
start | 55948945 |
end | 56033361 |
strand | + |
ver | v1.2 |
region | chr4:55948945-56033361 |
region5000 | chr4:55943945-56038361 |
regionname0 | CEP135_chr4_55948945_56033361 |
regionname5000 | CEP135_chr4_55943945_56038361 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1140 | 274 | 59 | 55 | 119 | 12 | 27 | 101 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0002 | 0/0 | 1140 | 48 | 7 | 10 | 23 | 2 | 6 | 20 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0003 | 0/0 | 1140 | 5 | 0 | 2 | 0 | 2 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0004 | 0/0 | 1140 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0005 | 0/0 | 1140 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0006 | 0/0 | 1140 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0007 | 0/0 | 1140 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0008 | 0/0 | 1140 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0009 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0010 | 0/0 | 1140 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0011 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0012 | 0/0 | 1140 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0013 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 3423 | 257 | 56 | 44 | 117 | 12 | 26 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
c0002 | 0/0 | 3423 | 48 | 7 | 10 | 23 | 2 | 6 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
c0003 | 0/0 | 3423 | 11 | 2 | 7 | 1 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
c0004 | 0/0 | 3423 | 5 | 0 | 2 | 0 | 2 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
c0005 | 0/0 | 3423 | 4 | 4 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
c0006 | 0/0 | 3423 | 4 | 4 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
c0007 | 0/0 | 3423 | 3 | 0 | 3 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
c0008 | 0/0 | 3423 | 2 | 1 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
c0009 | 0/0 | 3423 | 2 | 0 | 2 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
c0010 | 0/0 | 3423 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
c0011 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
c0012 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
c0013 | 0/0 | 3423 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
c0014 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
c0015 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
c0016 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
c0017 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
c0018 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2174 | 89 | 17 | 12 | 50 | 3 | 6 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0002 | 0/0 | 2183 | 79 | 3 | 11 | 52 | 3 | 10 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0003 | 0/0 | 2175 | 59 | 8 | 18 | 22 | 4 | 7 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0004 | 0/0 | 2183 | 33 | 8 | 10 | 12 | 1 | 2 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0005 | 0/1 | 2174 | 24 | 8 | 5 | 1 | 3 | 6 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0006 | 0/0 | 2173 | 13 | 3 | 4 | 3 | 2 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0007 | 0/0 | 2177 | 5 | 5 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0008 | 0/0 | 2178 | 5 | 5 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0009 | 0/0 | 2176 | 4 | 2 | 1 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0010 | 0/0 | 2185 | 4 | 2 | 1 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0011 | 0/0 | 2181 | 4 | 2 | 2 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0012 | 0/0 | 2176 | 4 | 3 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0013 | 0/0 | 2181 | 3 | 2 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0014 | 0/0 | 2181 | 2 | 2 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0015 | 0/0 | 2177 | 2 | 1 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0016 | 0/0 | 2174 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0017 | 0/0 | 2175 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0018 | 0/0 | 2174 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0019 | 0/0 | 2183 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0020 | 0/0 | 2173 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0021 | 0/0 | 2184 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0022 | 0/0 | 2184 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0023 | 0/0 | 2173 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0024 | 0/0 | 2185 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0025 | 0/0 | 2185 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0026 | 0/0 | 2174 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0027 | 0/0 | 2183 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0028 | 0/0 | 2174 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0029 | 0/0 | 2174 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0030 | 0/0 | 2174 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
t0031 | 0/0 | 2173 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 1/0 | 6 | 1 | 1 | 3 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0002 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0003 | 0/0 | 5 | 1 | 3 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0006 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0239 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3423 | 257 | 56 | 44 | 117 | 12 | 26 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0003 | 0/0 | 3423 | 11 | 2 | 7 | 1 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0007 | 0/0 | 3423 | 3 | 0 | 3 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0013 | 0/0 | 3423 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0015 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0016 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0002c0002 | 0/0 | 3423 | 48 | 7 | 10 | 23 | 2 | 6 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0003c0004 | 0/0 | 3423 | 5 | 0 | 2 | 0 | 2 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0004c0005 | 0/0 | 3423 | 4 | 4 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0005c0006 | 0/0 | 3423 | 4 | 4 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0006c0008 | 0/0 | 3423 | 2 | 1 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0007c0009 | 0/0 | 3423 | 2 | 0 | 2 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0008c0010 | 0/0 | 3423 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0009c0018 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0010c0017 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0011c0012 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0012c0014 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0013c0011 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5596 | 80 | 13 | 9 | 48 | 3 | 6 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0002 | 0/0 | 5605 | 76 | 3 | 9 | 51 | 3 | 10 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0003 | 0/0 | 5597 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0004 | 0/0 | 5605 | 31 | 8 | 10 | 10 | 1 | 2 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0005 | 0/1 | 5596 | 22 | 7 | 4 | 1 | 3 | 6 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0006 | 0/0 | 5595 | 10 | 3 | 4 | 0 | 2 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0007 | 0/0 | 5599 | 5 | 5 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0009 | 0/0 | 5598 | 4 | 2 | 1 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0010 | 0/0 | 5607 | 4 | 2 | 1 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0011 | 0/0 | 5603 | 2 | 1 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0012 | 0/0 | 5598 | 4 | 3 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0013 | 0/0 | 5603 | 3 | 2 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0014 | 0/0 | 5603 | 2 | 2 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0016 | 0/0 | 5596 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0019 | 0/0 | 5605 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0020 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0021 | 0/0 | 5606 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0022 | 0/0 | 5606 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0023 | 0/0 | 5595 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0024 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0025 | 0/0 | 5607 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0026 | 0/0 | 5596 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0028 | 0/0 | 5596 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0029 | 0/0 | 5596 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0030 | 0/0 | 5596 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0001t0031 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0003t0003 | 0/0 | 5597 | 11 | 2 | 7 | 1 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0007t0001 | 0/0 | 5596 | 3 | 0 | 3 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0013t0005 | 0/0 | 5596 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0015t0004 | 0/0 | 5605 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0001c0016t0027 | 0/0 | 5605 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0002c0002t0003 | 0/0 | 5597 | 41 | 6 | 9 | 19 | 2 | 5 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0002c0002t0004 | 0/0 | 5605 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0002c0002t0006 | 0/0 | 5595 | 3 | 0 | 0 | 3 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0002c0002t0015 | 0/0 | 5599 | 2 | 1 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0002c0002t0017 | 0/0 | 5597 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0003c0004t0003 | 0/0 | 5597 | 5 | 0 | 2 | 0 | 2 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0004c0005t0001 | 0/0 | 5596 | 4 | 4 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0005c0006t0008 | 0/0 | 5600 | 4 | 4 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0006c0008t0011 | 0/0 | 5603 | 2 | 1 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0007c0009t0002 | 0/0 | 5605 | 2 | 0 | 2 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0008c0010t0001 | 0/0 | 5596 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0009c0018t0018 | 0/0 | 5596 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0010c0017t0003 | 0/0 | 5597 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0011c0012t0008 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0012c0014t0002 | 0/0 | 5605 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
a0013c0011t0005 | 0/0 | 5596 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | copy fasta | chr4 | 55943945 | 56038361 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 5 | 0 | 1 | 3 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0004g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0239 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0005g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0006g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0006g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0006g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0006g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0006g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0006g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0007g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0009g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0009g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0009g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0009g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0010g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0010g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0011g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0012g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0012g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0012g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0012g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0013g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0013g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0013g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0014g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0014g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0016g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0019g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0020g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0021g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0022g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0023g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0024g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0025g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0026g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0028g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0029g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0030g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0001t0031g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0003t0003g0003 | 0/0 | 5 | 1 | 3 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0003t0003g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0003t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0003t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0003t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0003t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0007t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0007t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0013t0005g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0015t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0001c0016t0027g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0002 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0006g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0015g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0015g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0002c0002t0017g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0003c0004t0003g0006 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0003c0004t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0003c0004t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0004c0005t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0004c0005t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0004c0005t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0004c0005t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0005c0006t0008g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0005c0006t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0005c0006t0008g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0005c0006t0008g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0006c0008t0011g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0006c0008t0011g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0007c0009t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0007c0009t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0008c0010t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0008c0010t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0009c0018t0018g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0010c0017t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0011c0012t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0012c0014t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
a0013c0011t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0105 | EUR | GBR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0017 | EUR | GBR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00280 | hp1 | a0001 | c0001 | t0006 | g0051 | EUR | FIN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0250 | EUR | FIN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00323 | hp1 | a0001 | c0001 | t0006 | g0047 | EUR | FIN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00323 | hp2 | a0001 | c0001 | t0005 | g0249 | EUR | FIN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00408 | hp1 | a0001 | c0001 | t0004 | g0287 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00408 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00558 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00639 | hp1 | a0001 | c0001 | t0025 | g0007 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00639 | hp2 | a0002 | c0002 | t0003 | g0140 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0031 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00673 | hp2 | a0012 | c0014 | t0002 | g0097 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00733 | hp1 | a0001 | c0001 | t0006 | g0046 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00733 | hp2 | a0003 | c0004 | t0003 | g0141 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00735 | hp1 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0281 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00738 | hp1 | a0001 | c0001 | t0005 | g0309 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00738 | hp2 | a0003 | c0004 | t0003 | g0006 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0282 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01069 | hp1 | a0001 | c0003 | t0003 | g0274 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01070 | hp1 | a0001 | c0007 | t0001 | g0016 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01071 | hp1 | a0001 | c0003 | t0003 | g0273 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01071 | hp2 | a0001 | c0007 | t0001 | g0016 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01099 | hp1 | a0001 | c0013 | t0005 | g0189 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01099 | hp2 | a0002 | c0002 | t0015 | g0164 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01106 | hp2 | a0002 | c0002 | t0003 | g0132 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0045 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01167 | hp1 | a0001 | c0007 | t0001 | g0228 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01167 | hp2 | a0001 | c0001 | t0012 | g0160 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0283 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01175 | hp1 | a0001 | c0003 | t0003 | g0003 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0303 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01192 | hp1 | a0001 | c0001 | t0005 | g0245 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01192 | hp2 | a0002 | c0002 | t0003 | g0163 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01243 | hp1 | a0002 | c0002 | t0003 | g0162 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01243 | hp2 | a0006 | c0008 | t0011 | g0028 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01255 | hp1 | a0001 | c0001 | t0030 | g0153 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01256 | hp1 | a0002 | c0002 | t0003 | g0152 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01256 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01257 | hp1 | a0001 | c0001 | t0009 | g0213 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01257 | hp2 | a0002 | c0002 | t0003 | g0014 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01258 | hp2 | a0002 | c0002 | t0003 | g0014 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01346 | hp1 | a0001 | c0003 | t0003 | g0019 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01358 | hp1 | a0002 | c0002 | t0003 | g0148 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01358 | hp2 | a0007 | c0009 | t0002 | g0095 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01361 | hp1 | a0007 | c0009 | t0002 | g0115 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01433 | hp2 | a0002 | c0002 | t0003 | g0263 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01515 | hp1 | a0002 | c0002 | t0003 | g0138 | EUR | IBS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01515 | hp2 | a0001 | c0001 | t0005 | g0254 | EUR | IBS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0114 | EUR | IBS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | IBS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01517 | hp1 | a0002 | c0002 | t0003 | g0002 | EUR | IBS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0066 | EUR | IBS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01884 | hp2 | a0002 | c0002 | t0003 | g0265 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01928 | hp1 | a0001 | c0003 | t0003 | g0003 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01928 | hp2 | a0001 | c0001 | t0023 | g0117 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01943 | hp1 | a0001 | c0003 | t0003 | g0003 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01943 | hp2 | a0001 | c0001 | t0006 | g0049 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01981 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01993 | hp1 | a0001 | c0001 | t0005 | g0246 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG01993 | hp2 | a0001 | c0003 | t0003 | g0276 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02004 | hp2 | a0001 | c0001 | t0013 | g0007 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0289 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02055 | hp2 | a0002 | c0002 | t0003 | g0130 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02083 | hp2 | a0001 | c0001 | t0004 | g0277 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02129 | hp1 | a0002 | c0002 | t0003 | g0129 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0200 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02148 | hp1 | a0001 | c0001 | t0004 | g0306 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02148 | hp2 | a0001 | c0001 | t0010 | g0008 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02155 | hp1 | a0002 | c0002 | t0003 | g0136 | EAS | CDX | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0300 | EAS | CDX | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02257 | hp1 | a0001 | c0001 | t0006 | g0048 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0237 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02258 | hp1 | a0001 | c0001 | t0007 | g0004 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02258 | hp2 | a0001 | c0001 | t0020 | g0268 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0293 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02280 | hp2 | a0001 | c0001 | t0007 | g0004 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02300 | hp1 | a0001 | c0001 | t0011 | g0026 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02451 | hp1 | a0001 | c0001 | t0024 | g0307 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02451 | hp2 | a0001 | c0003 | t0003 | g0275 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02523 | hp1 | a0001 | c0001 | t0022 | g0116 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02572 | hp1 | a0001 | c0001 | t0012 | g0155 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02572 | hp2 | a0001 | c0001 | t0009 | g0199 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02615 | hp2 | a0001 | c0001 | t0012 | g0156 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02622 | hp2 | a0004 | c0005 | t0001 | g0180 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0126 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02647 | hp2 | a0001 | c0001 | t0019 | g0280 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0301 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02717 | hp1 | a0001 | c0001 | t0014 | g0032 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02717 | hp2 | a0001 | c0001 | t0009 | g0001 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02723 | hp1 | a0001 | c0001 | t0007 | g0004 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0233 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02735 | hp1 | a0002 | c0002 | t0003 | g0002 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0291 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02886 | hp1 | a0013 | c0011 | t0005 | g0165 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02896 | hp1 | a0001 | c0001 | t0010 | g0057 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0127 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02922 | hp1 | a0001 | c0001 | t0012 | g0158 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02970 | hp2 | a0001 | c0016 | t0027 | g0278 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02976 | hp1 | a0001 | c0001 | t0014 | g0033 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02976 | hp2 | a0005 | c0006 | t0008 | g0161 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03017 | hp1 | a0001 | c0003 | t0003 | g0019 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03017 | hp2 | a0002 | c0002 | t0003 | g0151 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03098 | hp2 | a0002 | c0002 | t0003 | g0013 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0292 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03130 | hp2 | a0004 | c0005 | t0001 | g0217 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03139 | hp1 | a0002 | c0002 | t0003 | g0135 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03139 | hp2 | a0004 | c0005 | t0001 | g0241 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0044 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0238 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03225 | hp2 | a0002 | c0002 | t0003 | g0149 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03239 | hp2 | a0001 | c0001 | t0005 | g0248 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03453 | hp1 | a0001 | c0001 | t0010 | g0056 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03486 | hp1 | a0005 | c0006 | t0008 | g0157 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03486 | hp2 | a0011 | c0012 | t0008 | g0181 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03492 | hp1 | a0002 | c0002 | t0017 | g0308 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0027 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0043 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0288 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0220 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03710 | hp1 | a0001 | c0001 | t0006 | g0050 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03710 | hp2 | a0001 | c0001 | t0005 | g0244 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03831 | hp2 | a0001 | c0001 | t0005 | g0017 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03834 | hp2 | a0003 | c0004 | t0003 | g0143 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03927 | hp1 | a0001 | c0001 | t0005 | g0212 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0182 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0285 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0082 | SAS | STU | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG04115 | hp2 | a0002 | c0002 | t0003 | g0128 | SAS | STU | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG04184 | hp2 | a0001 | c0001 | t0016 | g0177 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | STU | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG04204 | hp2 | a0002 | c0002 | t0003 | g0235 | SAS | STU | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | STU | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | STU | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18522 | hp1 | a0006 | c0008 | t0011 | g0029 | AFR | YRI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0243 | AFR | YRI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | YRI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0294 | AFR | YRI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18940 | hp2 | a0002 | c0002 | t0003 | g0133 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18948 | hp2 | a0002 | c0002 | t0006 | g0142 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18950 | hp2 | a0002 | c0002 | t0003 | g0134 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18952 | hp2 | a0002 | c0002 | t0003 | g0147 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18961 | hp1 | a0001 | c0001 | t0004 | g0298 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18961 | hp2 | a0002 | c0002 | t0003 | g0120 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18968 | hp1 | a0002 | c0002 | t0006 | g0150 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18974 | hp2 | a0001 | c0001 | t0009 | g0063 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18975 | hp1 | a0002 | c0002 | t0003 | g0137 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0299 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18979 | hp1 | a0002 | c0002 | t0003 | g0121 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18979 | hp2 | a0001 | c0001 | t0026 | g0257 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18983 | hp2 | a0001 | c0015 | t0004 | g0286 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18986 | hp1 | a0002 | c0002 | t0003 | g0264 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18988 | hp1 | a0010 | c0017 | t0003 | g0002 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18989 | hp1 | a0008 | c0010 | t0001 | g0231 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18994 | hp1 | a0002 | c0002 | t0003 | g0139 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18995 | hp1 | a0002 | c0002 | t0003 | g0118 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18995 | hp2 | a0008 | c0010 | t0001 | g0234 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19002 | hp2 | a0001 | c0001 | t0005 | g0218 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0302 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19006 | hp1 | a0001 | c0001 | t0010 | g0106 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19007 | hp2 | a0002 | c0002 | t0003 | g0144 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19010 | hp1 | a0002 | c0002 | t0003 | g0146 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0290 | AFR | LWK | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | LWK | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0053 | AFR | LWK | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19043 | hp2 | a0002 | c0002 | t0003 | g0042 | AFR | LWK | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19057 | hp1 | a0001 | c0001 | t0028 | g0178 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19057 | hp2 | a0002 | c0002 | t0003 | g0090 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19058 | hp1 | a0001 | c0001 | t0029 | g0193 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19062 | hp1 | a0002 | c0002 | t0003 | g0119 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0297 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19079 | hp1 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19081 | hp1 | a0002 | c0002 | t0006 | g0002 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19082 | hp2 | a0001 | c0001 | t0004 | g0304 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19084 | hp1 | a0002 | c0002 | t0003 | g0310 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19088 | hp2 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19090 | hp1 | a0002 | c0002 | t0004 | g0145 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19240 | hp1 | a0001 | c0001 | t0013 | g0270 | AFR | YRI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA19240 | hp2 | a0009 | c0018 | t0018 | g0271 | AFR | YRI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA20129 | hp1 | a0001 | c0001 | t0011 | g0025 | AFR | ASW | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA20129 | hp2 | a0005 | c0006 | t0008 | g0154 | AFR | ASW | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA20752 | hp2 | a0003 | c0004 | t0003 | g0006 | EUR | TSI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0305 | EUR | TSI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA20805 | hp2 | a0003 | c0004 | t0003 | g0006 | EUR | TSI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | GIH | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA20905 | hp2 | a0002 | c0002 | t0003 | g0034 | SAS | GIH | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02109 | hp1 | a0001 | c0001 | t0031 | g0131 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03471 | hp1 | a0002 | c0002 | t0015 | g0013 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0295 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG06807 | hp1 | a0001 | c0001 | t0021 | g0124 | AFR | USA | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | USA | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA20300 | hp1 | a0001 | c0003 | t0003 | g0003 | AFR | USA | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA20300 | hp2 | a0004 | c0005 | t0001 | g0242 | AFR | USA | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA21309 | hp1 | a0001 | c0001 | t0013 | g0269 | AFR | LWK | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
NA21309 | hp2 | a0005 | c0006 | t0008 | g0159 | AFR | LWK | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0239 | REF | REF | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:55952134
|
A | G | 1 | a0009 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.4A>G | p.Thr2Ala | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 2/26 | 164/5596 | 4/3423 | 2/1140 | chr4 | 55952134 | ||
chr4:55954246
|
G | A | 1 | a0003 | 5 | HG00733.hp2 HG00738.hp2 HG03834.hp2 others(2): Show |
missense_variant | MODERATE | c.335G>A | p.Arg112His | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/26 | 495/5596 | 335/3423 | 112/1140 | chr4 | 55954246 | ||
chr4:55959687
|
A | C | 1 | a0010 | 1 | NA18988.hp1 | missense_variant | MODERATE | c.620A>C | p.Gln207Pro | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/26 | 780/5596 | 620/3423 | 207/1140 | chr4 | 55959687 | ||
chr4:55959753
|
A | G | 1 | a0008 | 2 | NA18989.hp1 NA18995.hp2 |
missense_variant | MODERATE | c.686A>G | p.Asp229Gly | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/26 | 846/5596 | 686/3423 | 229/1140 | chr4 | 55959753 | ||
chr4:55965752
|
G | A | 1 | a0013 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.937G>A | p.Glu313Lys | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/26 | 1097/5596 | 937/3423 | 313/1140 | chr4 | 55965752 | ||
chr4:55971379
|
G | A | 2 | a0004a0011 | 5 | HG02622.hp2 HG03130.hp2 HG03139.hp2 others(2): Show |
missense_variant | MODERATE | c.1220G>A | p.Ser407Asn | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/26 | 1380/5596 | 1220/3423 | 407/1140 | chr4 | 55971379 | ||
chr4:55974909
|
A | T | 1 | a0012 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.1413A>T | p.Arg471Ser | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/26 | 1573/5596 | 1413/3423 | 471/1140 | chr4 | 55974909 | ||
chr4:55981275
|
G | A | 1 | a0005 | 4 | HG02976.hp2 HG03486.hp1 NA20129.hp2 others(1): Show |
missense_variant | MODERATE | c.1675G>A | p.Ala559Thr | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/26 | 1835/5596 | 1675/3423 | 559/1140 | chr4 | 55981275 | ||
chr4:56008351
|
A | C | 3 | a0002a0003a0010 | 54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
missense_variant | MODERATE | c.2305A>C | p.Ile769Leu | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/26 | 2465/5596 | 2305/3423 | 769/1140 | chr4 | 56008351 | ||
chr4:56009796
|
G | C | 1 | a0011 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.2398G>C | p.Asp800His | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/26 | 2558/5596 | 2398/3423 | 800/1140 | chr4 | 56009796 | ||
chr4:56020725
|
T | A | 1 | a0006 | 2 | HG01243.hp2 NA18522.hp1 |
missense_variant | MODERATE | c.3265T>A | p.Leu1089Ile | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/26 | 3425/5596 | 3265/3423 | 1089/1140 | chr4 | 56020725 | ||
chr4:56024527
|
G | A | 1 | a0007 | 2 | HG01358.hp2 HG01361.hp1 |
missense_variant | MODERATE | c.3347G>A | p.Arg1116Gln | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/26 | 3507/5596 | 3347/3423 | 1116/1140 | chr4 | 56024527 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:55974750
|
A | G | 1 | a0001c0016 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.1254A>G | p.Arg418Arg | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/26 | 1414/5596 | 1254/3423 | 418/1140 | chr4 | 55974750 | ||
chr4:55974855
|
A | G | 1 | a0001c0015 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.1359A>G | p.Glu453Glu | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/26 | 1519/5596 | 1359/3423 | 453/1140 | chr4 | 55974855 | ||
chr4:55981340
|
A | G | 1 | a0001c0013 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.1740A>G | p.Arg580Arg | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/26 | 1900/5596 | 1740/3423 | 580/1140 | chr4 | 55981340 | ||
chr4:56011907
|
A | G | 1 | a0013c0011 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.2724A>G | p.Arg908Arg | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/26 | 2884/5596 | 2724/3423 | 908/1140 | chr4 | 56011907 | ||
chr4:56011938
|
A | C | 1 | a0001c0007 | 3 | HG01070.hp1 HG01071.hp2 HG01167.hp1 |
synonymous_variant | LOW | c.2755A>C | p.Arg919Arg | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/26 | 2915/5596 | 2755/3423 | 919/1140 | chr4 | 56011938 | ||
chr4:56017821
|
C | G | 1 | a0001c0003 | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
synonymous_variant | LOW | c.2976C>G | p.Thr992Thr | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/26 | 3136/5596 | 2976/3423 | 992/1140 | chr4 | 56017821 | ||
chr4:56019415
|
T | C | 1 | a0001c0003 | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
synonymous_variant | LOW | c.3075T>C | p.Asn1025Asn | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/26 | 3235/5596 | 3075/3423 | 1025/1140 | chr4 | 56019415 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:55948964
|
G | T | 1 | a0001c0001t0031 | 1 | HG02109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-141G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/26 | 3167 | chr4 | 55948964 | |||||
chr4:55948979
|
T | C | 6 | a0001c0001t0005a0001c0001t0016a0001c0013t0005others(3): Show | 27 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-126T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/26 | 3152 | chr4 | 55948979 | |||||
chr4:56031397
|
A | C | 4 | a0001c0001t0012a0001c0001t0030a0005c0006t0008others(1): Show | 10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*49A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 6794 | chr4 | 56031397 | |||||
chr4:56031562
|
C | T | 3 | a0001c0001t0007a0001c0001t0011a0006c0008t0011 | 9 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*214C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 6959 | chr4 | 56031562 | |||||
chr4:56031851
|
T | C | 4 | a0001c0001t0012a0001c0001t0030a0005c0006t0008others(1): Show | 10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*503T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7248 | chr4 | 56031851 | |||||
chr4:56031856
|
G | C | 1 | a0001c0001t0019 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*508G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7253 | chr4 | 56031856 | |||||
chr4:56032046
|
A | G | 1 | a0001c0001t0029 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*698A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7443 | chr4 | 56032046 | |||||
chr4:56032050
|
A | G | 1 | a0001c0001t0028 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*702A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7447 | chr4 | 56032050 | |||||
chr4:56032074
|
A | G | 1 | a0001c0016t0027 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*726A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7471 | chr4 | 56032074 | |||||
chr4:56032167
|
G | A | 1 | a0001c0001t0020 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*819G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7564 | chr4 | 56032167 | |||||
chr4:56032173
|
A | G | 1 | a0001c0001t0026 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*825A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7570 | chr4 | 56032173 | |||||
chr4:56032218
|
G | A | 1 | a0001c0001t0021 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*870G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7615 | chr4 | 56032218 | |||||
chr4:56032248
|
C | G | 1 | a0009c0018t0018 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*900C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7645 | chr4 | 56032248 | |||||
chr4:56032288
|
T | C | 1 | a0001c0001t0016 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*940T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7685 | chr4 | 56032288 | |||||
chr4:56032446
|
GA | G | 28 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(25): Show | 212 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*1111delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7856 | INFO_REALIGN_3_PRIME | chr4 | 56032446 | ||||
chr4:56032470
|
T | A | 2 | a0001c0001t0014a0001c0016t0027 | 3 | HG02717.hp1 HG02970.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1122T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7867 | chr4 | 56032470 | |||||
chr4:56032628
|
T | G | 3 | a0001c0001t0007a0001c0001t0011a0006c0008t0011 | 9 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1280T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 8025 | chr4 | 56032628 | |||||
chr4:56032847
|
A | AGT | 8 | a0001c0001t0003a0001c0001t0009a0001c0001t0012others(5): Show | 68 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1522_*1523dupGT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 8269 | INFO_REALIGN_3_PRIME | chr4 | 56032847 | ||||
chr4:56032847
|
A | AGTGT | 4 | a0001c0001t0007a0002c0002t0015a0005c0006t0008others(1): Show | 12 | HG01099.hp2 HG02258.hp1 HG02280.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1520_*1523dupGTGT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 8269 | INFO_REALIGN_3_PRIME | chr4 | 56032847 | ||||
chr4:56032847
|
A | AGTGTGTG others(1): Show |
4 | a0001c0001t0011a0001c0001t0013a0001c0001t0014others(1): Show | 9 | HG01243.hp2 HG02004.hp2 HG02300.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1516_*1523dupGTGT others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 8269 | INFO_REALIGN_3_PRIME | chr4 | 56032847 | ||||
chr4:56032847
|
A | AGTGTGTG others(3): Show |
10 | a0001c0001t0002a0001c0001t0004a0001c0001t0019others(7): Show | 116 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*1514_*1523dupGTGT others(6): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 8269 | INFO_REALIGN_3_PRIME | chr4 | 56032847 | ||||
chr4:56032847
|
A | AGTGTGTG others(5): Show |
3 | a0001c0001t0010a0001c0001t0024a0001c0001t0025 | 6 | HG00639.hp1 HG02148.hp2 HG02451.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1512_*1523dupGTGT others(8): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 8269 | INFO_REALIGN_3_PRIME | chr4 | 56032847 | ||||
chr4:56032848
|
G | A | 1 | a0001c0001t0020 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1500G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 8245 | chr4 | 56032848 | |||||
chr4:56033078
|
C | A | 1 | a0001c0001t0024 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1730C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 8475 | chr4 | 56033078 | |||||
chr4:56033211
|
A | G | 6 | a0001c0001t0002a0001c0001t0010a0001c0001t0022others(3): Show | 85 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1863A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 8608 | chr4 | 56033211 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:55949238
|
C | T | 1 | a0002c0002t0003g0310 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-46+179C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55949238 | ||||||
chr4:55949253
|
C | G | 1 | a0001c0001t0005g0309 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-46+194C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55949253 | ||||||
chr4:55949273
|
G | A | 1 | a0001c0001t0002g0023 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-46+214G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55949273 | ||||||
chr4:55949331
|
C | G | 1 | a0002c0002t0017g0308 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-46+272C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55949331 | ||||||
chr4:55949332
|
G | T | 1 | a0002c0002t0017g0308 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-46+273G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55949332 | ||||||
chr4:55949714
|
C | T | 33 | a0001c0001t0001g0296a0001c0001t0002g0284a0001c0001t0004g0007others(30): Show | 36 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.-46+655C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55949714 | ||||||
chr4:55949765
|
T | A | 1 | a0001c0001t0005g0024 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-46+706T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55949765 | ||||||
chr4:55950000
|
A | C | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-46+941A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55950000 | ||||||
chr4:55950091
|
GTCTC | G | 6 | a0001c0001t0007g0004a0001c0001t0007g0027a0001c0001t0011g0025others(3): Show | 8 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-46+1034_-46+1037d others(6): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr4 | 55950091 | |||||
chr4:55950096
|
T | A | 6 | a0001c0001t0007g0004a0001c0001t0007g0027a0001c0001t0011g0025others(3): Show | 8 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-46+1037T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55950096 | ||||||
chr4:55950331
|
G | C | 1 | a0001c0001t0002g0030 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-46+1272G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55950331 | ||||||
chr4:55950378
|
T | G | 1 | a0001c0001t0006g0031 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-46+1319T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55950378 | ||||||
chr4:55950423
|
G | C | 2 | a0001c0001t0014g0032a0001c0001t0014g0033 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-46+1364G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55950423 | ||||||
chr4:55950640
|
T | TA | 6 | a0001c0001t0004g0007a0001c0001t0004g0281a0001c0001t0004g0282others(3): Show | 6 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.-45-1434dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr4 | 55950640 | |||||
chr4:55950679
|
T | C | 1 | a0001c0001t0004g0283 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-45-1407T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55950679 | ||||||
chr4:55950723
|
A | G | 1 | a0001c0001t0002g0279 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-45-1363A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55950723 | ||||||
chr4:55950759
|
C | CT | 33 | a0001c0001t0001g0296a0001c0001t0004g0007a0001c0001t0004g0020others(30): Show | 36 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.-45-1318dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr4 | 55950759 | |||||
chr4:55950798
|
C | CAT | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.-45-1286_-45-1285d others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr4 | 55950798 | |||||
chr4:55951534
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-45-552G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55951534 | ||||||
chr4:55951698
|
C | G | 1 | a0001c0001t0002g0272 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-45-388C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55951698 | ||||||
chr4:55951828
|
G | A | 3 | a0001c0001t0002g0037a0001c0001t0002g0038a0001c0001t0002g0039 | 3 | NA18955.hp1 NA19011.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-45-258G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55951828 | ||||||
chr4:55952021
|
C | T | 1 | a0009c0018t0018g0271 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-45-65C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55952021 | ||||||
chr4:55952335
|
A | G | 1 | a0001c0001t0024g0307 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.113+92A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 2/25 | chr4 | 55952335 | ||||||
chr4:55952545
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.113+302T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 2/25 | chr4 | 55952545 | ||||||
chr4:55952546
|
C | T | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.113+303C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 2/25 | chr4 | 55952546 | ||||||
chr4:55952654
|
G | A | 2 | a0001c0001t0014g0032a0001c0001t0014g0033 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.113+411G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 2/25 | chr4 | 55952654 | ||||||
chr4:55952682
|
C | T | 3 | a0001c0001t0013g0269a0001c0001t0013g0270a0001c0001t0020g0268 | 3 | HG02258.hp2 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.114-403C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 2/25 | chr4 | 55952682 | ||||||
chr4:55952875
|
A | G | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | NA18948.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.114-210A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 2/25 | chr4 | 55952875 | ||||||
chr4:55953514
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.304+239G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 3/25 | chr4 | 55953514 | ||||||
chr4:55953570
|
T | C | 1 | a0002c0002t0003g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.304+295T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 3/25 | chr4 | 55953570 | ||||||
chr4:55953943
|
C | T | 1 | a0002c0002t0003g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.305-273C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 3/25 | chr4 | 55953943 | ||||||
chr4:55954045
|
T | G | 10 | a0001c0001t0006g0031a0001c0001t0006g0043a0001c0001t0006g0044others(7): Show | 10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.305-171T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 3/25 | chr4 | 55954045 | ||||||
chr4:55954064
|
T | C | 86 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(83): Show | 92 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.305-152T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 3/25 | chr4 | 55954064 | ||||||
chr4:55954136
|
T | A | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.305-80T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 3/25 | chr4 | 55954136 | ||||||
chr4:55954401
|
C | T | 2 | a0001c0001t0013g0269a0001c0001t0013g0270 | 2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.472+18C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55954401 | ||||||
chr4:55954550
|
G | C | 2 | a0001c0001t0014g0032a0001c0001t0014g0033 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.472+167G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55954550 | ||||||
chr4:55954566
|
G | A | 1 | a0001c0001t0021g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.472+183G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55954566 | ||||||
chr4:55954604
|
A | G | 8 | a0001c0001t0006g0031a0001c0001t0006g0045a0001c0001t0006g0046others(5): Show | 8 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.472+221A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55954604 | ||||||
chr4:55954923
|
A | T | 1 | a0002c0002t0003g0264 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.472+540A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55954923 | ||||||
chr4:55954924
|
T | A | 1 | a0002c0002t0003g0264 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.472+541T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55954924 | ||||||
chr4:55954926
|
C | A | 1 | a0002c0002t0003g0264 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.472+543C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55954926 | ||||||
chr4:55954927
|
A | C | 1 | a0002c0002t0003g0264 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.472+544A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55954927 | ||||||
chr4:55954970
|
A | T | 2 | a0001c0001t0014g0032a0001c0001t0014g0033 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.472+587A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55954970 | ||||||
chr4:55955088
|
A | G | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.472+705A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55955088 | ||||||
chr4:55955145
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.472+762G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55955145 | ||||||
chr4:55955228
|
G | A | 1 | a0001c0001t0021g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.472+845G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55955228 | ||||||
chr4:55955465
|
G | A | 2 | a0001c0001t0005g0126a0001c0001t0005g0127 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.472+1082G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55955465 | ||||||
chr4:55955640
|
C | T | 90 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(87): Show | 98 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.472+1257C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55955640 | ||||||
chr4:55955999
|
A | G | 1 | a0002c0002t0003g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.473-1224A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55955999 | ||||||
chr4:55956177
|
C | CCTTAAAA others(7): Show |
1 | a0002c0002t0003g0263 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.473-1037_473-1036i others(16): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr4 | 55956177 | |||||
chr4:55956222
|
A | C | 2 | a0006c0008t0011g0028a0006c0008t0011g0029 | 2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.473-1001A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956222 | ||||||
chr4:55956441
|
C | G | 1 | a0001c0001t0001g0262 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.473-782C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956441 | ||||||
chr4:55956591
|
T | C | 50 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(47): Show | 55 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.473-632T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956591 | ||||||
chr4:55956695
|
C | T | 1 | a0001c0001t0002g0122 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.473-528C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956695 | ||||||
chr4:55956704
|
G | A | 1 | a0002c0002t0003g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.473-519G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956704 | ||||||
chr4:55956740
|
A | G | 1 | a0001c0003t0003g0276 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.473-483A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956740 | ||||||
chr4:55956801
|
C | T | 1 | a0002c0002t0003g0034 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.473-422C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956801 | ||||||
chr4:55956825
|
C | G | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | NA18954.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.473-398C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956825 | ||||||
chr4:55956885
|
A | G | 1 | a0001c0001t0004g0022 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.473-338A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956885 | ||||||
chr4:55956913
|
C | A | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.473-310C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956913 | ||||||
chr4:55957158
|
G | A | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.473-65G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55957158 | ||||||
chr4:55957563
|
A | G | 4 | a0002c0002t0003g0034a0002c0002t0003g0162a0002c0002t0003g0163others(1): Show | 4 | HG01099.hp2 HG01192.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.614+199A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55957563 | ||||||
chr4:55957609
|
C | T | 1 | a0005c0006t0008g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.614+245C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55957609 | ||||||
chr4:55957649
|
T | C | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.614+285T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55957649 | ||||||
chr4:55957679
|
A | C | 1 | a0006c0008t0011g0029 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.614+315A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55957679 | ||||||
chr4:55958256
|
G | A | 1 | a0001c0015t0004g0286 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.614+892G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55958256 | ||||||
chr4:55958743
|
C | T | 1 | a0001c0016t0027g0278 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.615-939C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55958743 | ||||||
chr4:55958744
|
G | A | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.615-938G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55958744 | ||||||
chr4:55958886
|
A | T | 32 | a0001c0001t0001g0296a0001c0001t0004g0007a0001c0001t0004g0020others(29): Show | 35 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.615-796A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55958886 | ||||||
chr4:55959469
|
T | C | 2 | a0001c0001t0004g0287a0001c0015t0004g0286 | 2 | HG00408.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.615-213T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55959469 | ||||||
chr4:55959492
|
C | CTG | 201 | a0001c0001t0001g0125a0001c0001t0001g0296a0001c0001t0002g0005others(198): Show | 222 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.615-189_615-188ins others(2): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr4 | 55959492 | |||||
chr4:55959622
|
G | A | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.615-60G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55959622 | ||||||
chr4:55960067
|
T | C | 34 | a0001c0001t0001g0296a0001c0001t0004g0007a0001c0001t0004g0020others(31): Show | 37 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.699+301T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55960067 | ||||||
chr4:55960129
|
A | G | 1 | a0001c0001t0006g0031 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.699+363A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55960129 | ||||||
chr4:55960300
|
TTTTG | T | 23 | a0001c0001t0004g0007a0001c0001t0004g0020a0001c0001t0004g0021others(20): Show | 26 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.699+542_699+545del others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55960300 | |||||
chr4:55960369
|
G | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.699+603G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55960369 | ||||||
chr4:55960913
|
G | A | 2 | a0001c0001t0010g0056a0001c0001t0010g0057 | 2 | HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.699+1147G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55960913 | ||||||
chr4:55960921
|
G | A | 123 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(120): Show | 133 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.699+1155G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55960921 | ||||||
chr4:55960925
|
C | CA | 135 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(132): Show | 149 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(146): Show |
intron_variant | MODIFIER | c.699+1183dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55960925 | |||||
chr4:55960925
|
C | CAA | 21 | a0001c0001t0002g0030a0001c0001t0002g0037a0001c0001t0002g0038others(18): Show | 21 | HG00423.hp2 HG01106.hp2 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.699+1182_699+1183d others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55960925 | |||||
chr4:55960925
|
CA | C | 10 | a0001c0001t0001g0259a0001c0001t0012g0155a0001c0001t0012g0156others(7): Show | 10 | HG01167.hp2 HG01884.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.699+1183delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55960925 | |||||
chr4:55960950
|
T | A | 2 | a0001c0001t0014g0032a0001c0001t0014g0033 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.699+1184T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55960950 | ||||||
chr4:55960988
|
C | T | 1 | a0001c0001t0023g0117 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.699+1222C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55960988 | ||||||
chr4:55961041
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.699+1275G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961041 | ||||||
chr4:55961101
|
C | CA | 15 | a0001c0001t0001g0186a0001c0001t0001g0190a0001c0001t0002g0030others(12): Show | 21 | HG00423.hp2 HG00558.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.699+1354dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961101 | |||||
chr4:55961101
|
CA | C | 37 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(34): Show | 40 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.699+1354delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961101 | |||||
chr4:55961101
|
CAAAAAAA others(3): Show |
C | 6 | a0001c0001t0007g0004a0001c0001t0007g0027a0001c0001t0011g0025others(3): Show | 8 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.699+1345_699+1354d others(12): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961101 | |||||
chr4:55961164
|
A | ATGT | 36 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(33): Show | 39 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.699+1401_699+1403d others(5): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961164 | |||||
chr4:55961168
|
T | G | 3 | a0001c0001t0004g0285a0001c0001t0004g0297a0001c0001t0004g0300 | 3 | HG02155.hp2 HG03942.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.699+1402T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961168 | ||||||
chr4:55961181
|
T | C | 1 | a0001c0001t0004g0301 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.699+1415T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961181 | ||||||
chr4:55961183
|
T | G | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.699+1417T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961183 | ||||||
chr4:55961245
|
G | A | 1 | a0001c0001t0002g0068 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.699+1479G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961245 | ||||||
chr4:55961322
|
A | G | 9 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(6): Show | 9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.699+1556A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961322 | ||||||
chr4:55961493
|
G | A | 5 | a0001c0001t0002g0009a0001c0001t0002g0023a0001c0001t0002g0093others(2): Show | 6 | HG02132.hp1 NA18984.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.699+1727G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961493 | ||||||
chr4:55961531
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.699+1765G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961531 | ||||||
chr4:55961624
|
T | C | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.699+1858T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961624 | ||||||
chr4:55961632
|
C | T | 1 | a0002c0002t0003g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.699+1866C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961632 | ||||||
chr4:55961637
|
T | C | 2 | a0001c0001t0004g0289a0001c0001t0004g0290 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.699+1871T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961637 | ||||||
chr4:55961764
|
T | TA | 34 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(31): Show | 34 | HG00558.hp1 HG00642.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.699+2029dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | |||||
chr4:55961764
|
T | TAA | 9 | a0001c0001t0001g0015a0001c0001t0001g0041a0001c0001t0001g0169others(6): Show | 10 | HG00609.hp1 HG01109.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.699+2028_699+2029d others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | |||||
chr4:55961764
|
T | TAAAAA | 17 | a0001c0001t0002g0055a0001c0001t0002g0061a0001c0001t0002g0083others(14): Show | 17 | HG00609.hp2 HG01346.hp2 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.699+2025_699+2029d others(7): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | |||||
chr4:55961764
|
T | TAAAAAA | 27 | a0001c0001t0002g0005a0001c0001t0002g0030a0001c0001t0002g0037others(24): Show | 30 | HG00423.hp2 HG01070.hp2 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.699+2024_699+2029d others(8): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | |||||
chr4:55961764
|
T | TAAAAAAA | 16 | a0001c0001t0002g0008a0001c0001t0002g0011a0001c0001t0002g0052others(13): Show | 17 | HG00140.hp1 HG00642.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.699+2023_699+2029d others(9): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | |||||
chr4:55961764
|
T | TAAAAAAA others(1): Show |
13 | a0001c0001t0002g0009a0001c0001t0002g0064a0001c0001t0002g0065others(10): Show | 14 | HG02080.hp2 HG02145.hp1 HG03579.hp1 others(11): Show |
intron_variant | MODIFIER | c.699+2022_699+2029d others(10): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | |||||
chr4:55961764
|
T | TAAAAAAA others(2): Show |
6 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0093others(3): Show | 6 | HG00673.hp2 HG03927.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.699+2021_699+2029d others(11): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | |||||
chr4:55961764
|
T | TAAAAAAA others(3): Show |
6 | a0001c0001t0002g0010a0001c0001t0002g0023a0001c0001t0002g0070others(3): Show | 7 | HG01358.hp2 HG02132.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.699+2020_699+2029d others(12): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | |||||
chr4:55961764
|
T | TAAAAAAA others(4): Show |
1 | a0001c0001t0002g0062 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.699+2019_699+2029d others(13): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | |||||
chr4:55961764
|
T | TAAAAAAA others(5): Show |
1 | a0001c0001t0002g0069 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.699+2018_699+2029d others(14): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | |||||
chr4:55961764
|
TA | T | 42 | a0001c0001t0001g0167a0001c0001t0001g0183a0001c0001t0001g0184others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.699+2029delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | |||||
chr4:55961764
|
TAA | T | 17 | a0001c0001t0001g0258a0001c0001t0007g0004a0001c0001t0007g0027others(14): Show | 19 | HG01106.hp2 HG01243.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.699+2028_699+2029d others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | |||||
chr4:55961764
|
TAAA | T | 32 | a0002c0002t0003g0002a0002c0002t0003g0014a0002c0002t0003g0034others(29): Show | 37 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.699+2027_699+2029d others(5): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | |||||
chr4:55961764
|
TAAAAAAA others(4): Show |
T | 3 | a0001c0001t0013g0269a0001c0001t0013g0270a0001c0001t0020g0268 | 3 | HG02258.hp2 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.699+2019_699+2029d others(13): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | |||||
chr4:55961764
|
TAAAAAAA others(8): Show |
T | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.699+2015_699+2029d others(17): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | |||||
chr4:55961764
|
TAAAAAAA others(9): Show |
T | 1 | a0001c0001t0022g0116 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.699+2014_699+2029d others(18): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | |||||
chr4:55961764
|
TAAAAAAA others(10): Show |
T | 1 | a0001c0001t0006g0051 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.699+2013_699+2029d others(19): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | |||||
chr4:55961765
|
A | T | 2 | a0001c0001t0004g0294a0001c0001t0004g0295 | 2 | HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.699+1999A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961765 | ||||||
chr4:55961766
|
A | T | 1 | a0001c0001t0005g0127 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.699+2000A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961766 | ||||||
chr4:55961823
|
T | C | 1 | a0002c0002t0003g0134 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.699+2057T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961823 | ||||||
chr4:55961830
|
T | C | 2 | a0001c0001t0005g0237a0001c0001t0005g0238 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.699+2064T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961830 | ||||||
chr4:55961966
|
T | C | 8 | a0001c0001t0004g0020a0001c0001t0004g0277a0001c0001t0004g0287others(5): Show | 9 | HG00408.hp1 HG02083.hp2 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.699+2200T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961966 | ||||||
chr4:55962106
|
A | AT | 9 | a0001c0001t0013g0269a0001c0001t0013g0270a0001c0001t0020g0268others(6): Show | 14 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.700-2157dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55962106 | |||||
chr4:55962106
|
AT | A | 41 | a0001c0001t0031g0131a0002c0002t0003g0002a0002c0002t0003g0013others(38): Show | 46 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.700-2157delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55962106 | |||||
chr4:55962131
|
C | G | 189 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(186): Show | 210 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.700-2143C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55962131 | ||||||
chr4:55962351
|
C | T | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.700-1923C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55962351 | ||||||
chr4:55962464
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.700-1810C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55962464 | ||||||
chr4:55962482
|
A | G | 1 | a0001c0016t0027g0278 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.700-1792A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55962482 | ||||||
chr4:55962500
|
C | G | 1 | a0001c0001t0001g0236 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.700-1774C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55962500 | ||||||
chr4:55962603
|
G | A | 3 | a0001c0001t0013g0269a0001c0001t0013g0270a0001c0001t0020g0268 | 3 | HG02258.hp2 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.700-1671G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55962603 | ||||||
chr4:55962683
|
CT | C | 188 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(185): Show | 209 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.700-1589delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55962683 | |||||
chr4:55962708
|
C | T | 1 | a0002c0002t0003g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.700-1566C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55962708 | ||||||
chr4:55962714
|
T | G | 46 | a0001c0001t0019g0280a0001c0001t0031g0131a0002c0002t0003g0002others(43): Show | 52 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.700-1560T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55962714 | ||||||
chr4:55962730
|
C | CT | 8 | a0001c0001t0001g0192a0001c0001t0001g0205a0001c0001t0001g0206others(5): Show | 8 | HG01884.hp2 HG02258.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.700-1530dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55962730 | |||||
chr4:55962730
|
C | CTT | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.700-1531_700-1530d others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55962730 | |||||
chr4:55962730
|
CT | C | 170 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0002g0005others(167): Show | 186 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.700-1530delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55962730 | |||||
chr4:55963195
|
T | A | 1 | a0001c0001t0001g0207 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.700-1079T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55963195 | ||||||
chr4:55963316
|
G | A | 199 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(196): Show | 220 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.700-958G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55963316 | ||||||
chr4:55963511
|
C | T | 1 | a0002c0002t0003g0235 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.700-763C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55963511 | ||||||
chr4:55963619
|
A | G | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.700-655A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55963619 | ||||||
chr4:55963788
|
T | C | 86 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(83): Show | 92 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.700-486T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55963788 | ||||||
chr4:55964143
|
C | T | 3 | a0002c0002t0003g0013a0002c0002t0003g0149a0002c0002t0015g0013 | 3 | HG03098.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.700-131C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55964143 | ||||||
chr4:55964151
|
T | G | 1 | a0013c0011t0005g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.700-123T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55964151 | ||||||
chr4:55964171
|
A | T | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.700-103A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55964171 | ||||||
chr4:55964439
|
A | G | 7 | a0002c0002t0003g0034a0002c0002t0003g0132a0002c0002t0003g0148others(4): Show | 7 | HG01099.hp2 HG01106.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.828+37A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 7/25 | chr4 | 55964439 | ||||||
chr4:55964482
|
G | C | 1 | a0002c0002t0003g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.828+80G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 7/25 | chr4 | 55964482 | ||||||
chr4:55964649
|
G | T | 1 | a0002c0002t0003g0147 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.828+247G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 7/25 | chr4 | 55964649 | ||||||
chr4:55964768
|
G | A | 40 | a0001c0001t0031g0131a0002c0002t0003g0002a0002c0002t0003g0013others(37): Show | 45 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.828+366G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 7/25 | chr4 | 55964768 | ||||||
chr4:55964930
|
C | T | 2 | a0001c0001t0014g0032a0001c0001t0014g0033 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.828+528C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 7/25 | chr4 | 55964930 | ||||||
chr4:55964958
|
A | G | 86 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(83): Show | 92 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.828+556A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 7/25 | chr4 | 55964958 | ||||||
chr4:55965167
|
C | T | 7 | a0001c0001t0007g0004a0001c0001t0007g0027a0001c0001t0011g0025others(4): Show | 9 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.829-477C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 7/25 | chr4 | 55965167 | ||||||
chr4:55965280
|
G | A | 188 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(185): Show | 209 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.829-364G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 7/25 | chr4 | 55965280 | ||||||
chr4:55965423
|
T | C | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.829-221T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 7/25 | chr4 | 55965423 | ||||||
chr4:55965881
|
T | A | 1 | a0001c0001t0016g0177 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1044+22T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55965881 | ||||||
chr4:55965938
|
C | G | 2 | a0001c0001t0014g0032a0001c0001t0014g0033 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1044+79C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55965938 | ||||||
chr4:55966007
|
C | T | 38 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(35): Show | 41 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.1044+148C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55966007 | ||||||
chr4:55966163
|
G | A | 1 | a0001c0001t0021g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1044+304G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55966163 | ||||||
chr4:55966205
|
C | CT | 33 | a0001c0001t0001g0296a0001c0001t0004g0007a0001c0001t0004g0020others(30): Show | 36 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.1044+355dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr4 | 55966205 | |||||
chr4:55966318
|
A | G | 9 | a0001c0001t0013g0269a0001c0001t0013g0270a0001c0001t0020g0268others(6): Show | 14 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1044+459A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55966318 | ||||||
chr4:55966328
|
A | C | 9 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(6): Show | 9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1044+469A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55966328 | ||||||
chr4:55966371
|
T | C | 86 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(83): Show | 92 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.1044+512T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55966371 | ||||||
chr4:55966501
|
T | C | 1 | a0002c0002t0003g0014 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1044+642T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55966501 | ||||||
chr4:55966555
|
C | G | 129 | a0001c0001t0001g0296a0001c0001t0002g0005a0001c0001t0002g0008others(126): Show | 140 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1044+696C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55966555 | ||||||
chr4:55966739
|
T | C | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1044+880T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55966739 | ||||||
chr4:55966959
|
C | A | 2 | a0001c0001t0014g0032a0001c0001t0014g0033 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1044+1100C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55966959 | ||||||
chr4:55967097
|
G | A | 86 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(83): Show | 92 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.1044+1238G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55967097 | ||||||
chr4:55967601
|
T | G | 1 | a0013c0011t0005g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1045-1462T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55967601 | ||||||
chr4:55967719
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1045-1344C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55967719 | ||||||
chr4:55967950
|
A | G | 2 | a0001c0001t0002g0070a0001c0001t0002g0072 | 2 | NA18952.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1045-1113A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55967950 | ||||||
chr4:55968204
|
A | T | 1 | a0002c0002t0003g0134 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1045-859A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968204 | ||||||
chr4:55968220
|
T | G | 189 | a0001c0001t0001g0296a0001c0001t0002g0005a0001c0001t0002g0008others(186): Show | 210 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.1045-843T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968220 | ||||||
chr4:55968235
|
T | C | 5 | a0001c0001t0004g0020a0001c0001t0004g0298a0001c0001t0004g0299others(2): Show | 6 | NA18961.hp1 NA18977.hp2 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-828T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968235 | ||||||
chr4:55968347
|
C | T | 1 | a0001c0001t0002g0038 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1045-716C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968347 | ||||||
chr4:55968368
|
A | G | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1045-695A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968368 | ||||||
chr4:55968374
|
G | GT | 10 | a0001c0001t0001g0036a0001c0001t0001g0232a0001c0001t0002g0082others(7): Show | 10 | HG01167.hp2 HG01981.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1045-673dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr4 | 55968374 | |||||
chr4:55968374
|
GT | G | 96 | a0001c0001t0001g0208a0001c0001t0002g0009a0001c0001t0002g0010others(93): Show | 107 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.1045-673delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr4 | 55968374 | |||||
chr4:55968374
|
GTT | G | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1045-674_1045-673d others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr4 | 55968374 | |||||
chr4:55968651
|
T | C | 9 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(6): Show | 9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1045-412T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968651 | ||||||
chr4:55968671
|
A | G | 1 | a0002c0002t0003g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1045-392A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968671 | ||||||
chr4:55968689
|
T | C | 1 | a0001c0001t0001g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1045-374T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968689 | ||||||
chr4:55968832
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1045-231C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968832 | ||||||
chr4:55968844
|
T | C | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1045-219T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968844 | ||||||
chr4:55968877
|
C | T | 3 | a0001c0001t0002g0122a0001c0001t0014g0032a0001c0001t0014g0033 | 3 | HG02717.hp1 HG02976.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1045-186C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968877 | ||||||
chr4:55968878
|
G | A | 1 | a0001c0001t0005g0024 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1045-185G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968878 | ||||||
chr4:55968938
|
T | A | 6 | a0001c0001t0007g0004a0001c0001t0007g0027a0001c0001t0011g0025others(3): Show | 8 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1045-125T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968938 | ||||||
chr4:55968948
|
G | T | 124 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(121): Show | 134 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1045-115G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968948 | ||||||
chr4:55969143
|
T | C | 32 | a0001c0001t0004g0007a0001c0001t0004g0020a0001c0001t0004g0021others(29): Show | 35 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1110+15T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55969143 | ||||||
chr4:55969247
|
C | T | 199 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(196): Show | 220 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1110+119C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55969247 | ||||||
chr4:55969277
|
A | G | 1 | a0013c0011t0005g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1110+149A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55969277 | ||||||
chr4:55969428
|
TA | T | 190 | a0001c0001t0001g0176a0001c0001t0001g0190a0001c0001t0001g0192others(187): Show | 211 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.1110+320delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr4 | 55969428 | |||||
chr4:55969428
|
TAA | T | 11 | a0001c0001t0002g0060a0001c0001t0002g0066a0001c0001t0002g0091others(8): Show | 11 | HG01099.hp2 HG01517.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1110+319_1110+320d others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr4 | 55969428 | |||||
chr4:55969444
|
A | G | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+316A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55969444 | ||||||
chr4:55969445
|
A | G | 2 | a0001c0001t0019g0280a0002c0002t0004g0145 | 2 | HG02647.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1110+317A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55969445 | ||||||
chr4:55969741
|
A | G | 7 | a0001c0001t0001g0041a0001c0001t0001g0123a0001c0001t0001g0204others(4): Show | 7 | HG02080.hp1 HG02523.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.1110+613A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55969741 | ||||||
chr4:55969904
|
G | A | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1110+776G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55969904 | ||||||
chr4:55969909
|
G | C | 3 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0232 | 3 | HG02615.hp1 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1110+781G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55969909 | ||||||
chr4:55969953
|
G | A | 1 | a0001c0016t0027g0278 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1110+825G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55969953 | ||||||
chr4:55970037
|
C | CT | 187 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(184): Show | 208 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.1110+923dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr4 | 55970037 | |||||
chr4:55970077
|
A | G | 199 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(196): Show | 220 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1110+949A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55970077 | ||||||
chr4:55970123
|
C | T | 1 | a0001c0001t0021g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1110+995C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55970123 | ||||||
chr4:55970585
|
C | T | 2 | a0001c0001t0014g0032a0001c0001t0014g0033 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1111-685C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55970585 | ||||||
chr4:55970668
|
G | A | 2 | a0001c0001t0011g0025a0011c0012t0008g0181 | 2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1111-602G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55970668 | ||||||
chr4:55970701
|
G | T | 2 | a0004c0005t0001g0180a0011c0012t0008g0181 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1111-569G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55970701 | ||||||
chr4:55970828
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1111-442C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55970828 | ||||||
chr4:55971205
|
ATCTT | A | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1111-64_1111-61del others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55971205 | ||||||
chr4:55971454
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1249+46C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55971454 | ||||||
chr4:55971926
|
G | A | 33 | a0001c0001t0004g0007a0001c0001t0004g0020a0001c0001t0004g0021others(30): Show | 36 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.1249+518G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55971926 | ||||||
chr4:55972292
|
G | A | 9 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(6): Show | 9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1249+884G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972292 | ||||||
chr4:55972358
|
G | A | 1 | a0001c0001t0002g0105 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1249+950G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972358 | ||||||
chr4:55972365
|
TA | T | 3 | a0001c0001t0013g0269a0001c0001t0013g0270a0001c0001t0020g0268 | 3 | HG02258.hp2 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1249+960delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr4 | 55972365 | |||||
chr4:55972390
|
G | C | 1 | a0001c0001t0029g0193 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1249+982G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972390 | ||||||
chr4:55972486
|
T | C | 1 | a0001c0001t0002g0089 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1249+1078T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972486 | ||||||
chr4:55972487
|
A | G | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1249+1079A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972487 | ||||||
chr4:55972629
|
C | G | 6 | a0001c0001t0002g0008a0001c0001t0002g0081a0001c0001t0002g0087others(3): Show | 6 | HG01346.hp2 HG01433.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1249+1221C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972629 | ||||||
chr4:55972749
|
A | T | 1 | a0002c0002t0003g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1249+1341A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972749 | ||||||
chr4:55972759
|
C | T | 4 | a0001c0001t0001g0179a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | NA18970.hp1 NA18979.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1249+1351C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972759 | ||||||
chr4:55972905
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1249+1497G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972905 | ||||||
chr4:55972985
|
C | T | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | NA18954.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1249+1577C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972985 | ||||||
chr4:55973206
|
C | T | 1 | a0001c0001t0031g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250-1540C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55973206 | ||||||
chr4:55973280
|
G | A | 9 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(6): Show | 9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1250-1466G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55973280 | ||||||
chr4:55973539
|
G | A | 1 | a0001c0001t0021g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1250-1207G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55973539 | ||||||
chr4:55973642
|
G | A | 1 | a0013c0011t0005g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1250-1104G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55973642 | ||||||
chr4:55973700
|
A | C | 127 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(124): Show | 138 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.1250-1046A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55973700 | ||||||
chr4:55973874
|
G | A | 188 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(185): Show | 209 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.1250-872G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55973874 | ||||||
chr4:55974061
|
A | G | 1 | a0001c0001t0005g0254 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1250-685A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55974061 | ||||||
chr4:55974135
|
A | G | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1250-611A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55974135 | ||||||
chr4:55974146
|
G | A | 1 | a0001c0001t0005g0239 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1250-600G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55974146 | ||||||
chr4:55974509
|
C | T | 9 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(6): Show | 9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1250-237C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55974509 | ||||||
chr4:55974584
|
T | C | 7 | a0001c0001t0007g0004a0001c0001t0007g0027a0001c0001t0011g0025others(4): Show | 9 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1250-162T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55974584 | ||||||
chr4:55974664
|
A | G | 4 | a0002c0002t0003g0034a0002c0002t0003g0162a0002c0002t0003g0163others(1): Show | 4 | HG01099.hp2 HG01192.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250-82A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55974664 | ||||||
chr4:55974680
|
A | G | 50 | a0001c0001t0013g0269a0001c0001t0013g0270a0001c0001t0019g0280others(47): Show | 56 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1250-66A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55974680 | ||||||
chr4:55975049
|
C | T | 6 | a0001c0001t0007g0004a0001c0001t0007g0027a0001c0001t0011g0025others(3): Show | 8 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1473+80C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55975049 | ||||||
chr4:55975157
|
A | G | 1 | a0002c0002t0003g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1473+188A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55975157 | ||||||
chr4:55975901
|
G | T | 1 | a0001c0001t0014g0032 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1473+932G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55975901 | ||||||
chr4:55975940
|
G | A | 6 | a0001c0001t0007g0004a0001c0001t0007g0027a0001c0001t0011g0025others(3): Show | 8 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1473+971G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55975940 | ||||||
chr4:55976048
|
G | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0211 | 2 | HG01069.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1473+1079G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55976048 | ||||||
chr4:55976131
|
C | T | 1 | a0001c0001t0002g0080 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1473+1162C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55976131 | ||||||
chr4:55976235
|
CA | C | 27 | a0001c0001t0007g0004a0001c0001t0007g0027a0001c0001t0011g0025others(24): Show | 34 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1473+1280delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr4 | 55976235 | |||||
chr4:55976246
|
A | G | 1 | a0001c0001t0020g0268 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1473+1277A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55976246 | ||||||
chr4:55976593
|
T | C | 3 | a0001c0001t0013g0269a0001c0001t0013g0270a0001c0001t0020g0268 | 3 | HG02258.hp2 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1473+1624T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55976593 | ||||||
chr4:55976708
|
A | T | 199 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(196): Show | 220 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1473+1739A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55976708 | ||||||
chr4:55976973
|
C | CT | 8 | a0001c0001t0001g0018a0001c0001t0001g0170a0001c0001t0001g0221others(5): Show | 9 | HG00280.hp1 HG00733.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1473+2017dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr4 | 55976973 | |||||
chr4:55976973
|
CT | C | 9 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(6): Show | 9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1473+2017delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr4 | 55976973 | |||||
chr4:55976979
|
T | G | 2 | a0001c0001t0014g0032a0001c0001t0014g0033 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1473+2010T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55976979 | ||||||
chr4:55976982
|
T | G | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1473+2013T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55976982 | ||||||
chr4:55976983
|
T | G | 161 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(158): Show | 175 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.1473+2014T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55976983 | ||||||
chr4:55976987
|
G | T | 4 | a0001c0001t0001g0207a0001c0001t0001g0222a0008c0010t0001g0231others(1): Show | 4 | NA18955.hp2 NA18989.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1473+2018G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55976987 | ||||||
chr4:55977005
|
A | G | 8 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0190others(5): Show | 8 | HG01884.hp1 HG02132.hp2 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.1473+2036A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55977005 | ||||||
chr4:55977191
|
A | G | 2 | a0002c0002t0003g0144a0002c0002t0003g0146 | 2 | NA19007.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1473+2222A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55977191 | ||||||
chr4:55977601
|
T | G | 12 | a0001c0001t0004g0007a0001c0001t0004g0021a0001c0001t0004g0022others(9): Show | 14 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1474-2542T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55977601 | ||||||
chr4:55977760
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1474-2383A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55977760 | ||||||
chr4:55977783
|
A | T | 189 | a0001c0001t0001g0296a0001c0001t0002g0005a0001c0001t0002g0008others(186): Show | 210 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.1474-2360A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55977783 | ||||||
chr4:55977883
|
G | C | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1474-2260G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55977883 | ||||||
chr4:55978167
|
A | AGGGAACT others(13): Show |
1 | a0001c0013t0005g0189 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1474-1974_1474-195 others(24): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr4 | 55978167 | |||||
chr4:55978320
|
T | C | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1474-1823T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55978320 | ||||||
chr4:55978534
|
C | G | 3 | a0001c0001t0013g0269a0001c0001t0013g0270a0001c0001t0020g0268 | 3 | HG02258.hp2 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1474-1609C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55978534 | ||||||
chr4:55978996
|
C | T | 9 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(6): Show | 9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1474-1147C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55978996 | ||||||
chr4:55979039
|
A | G | 1 | a0001c0001t0002g0111 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1474-1104A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55979039 | ||||||
chr4:55979120
|
A | G | 50 | a0001c0001t0013g0269a0001c0001t0013g0270a0001c0001t0019g0280others(47): Show | 56 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1474-1023A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55979120 | ||||||
chr4:55979122
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1474-1021A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55979122 | ||||||
chr4:55979149
|
A | G | 7 | a0001c0001t0007g0004a0001c0001t0007g0027a0001c0001t0011g0025others(4): Show | 9 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1474-994A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55979149 | ||||||
chr4:55979238
|
CT | C | 9 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(6): Show | 9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1474-896delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr4 | 55979238 | |||||
chr4:55979604
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1474-539G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55979604 | ||||||
chr4:55979605
|
C | T | 34 | a0001c0001t0001g0296a0001c0001t0004g0007a0001c0001t0004g0020others(31): Show | 37 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1474-538C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55979605 | ||||||
chr4:55980401
|
T | A | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1626+106T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 12/25 | chr4 | 55980401 | ||||||
chr4:55980585
|
A | C | 59 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(56): Show | 65 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.1626+290A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 12/25 | chr4 | 55980585 | ||||||
chr4:55980859
|
G | A | 1 | a0001c0001t0002g0083 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1627-368G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 12/25 | chr4 | 55980859 | ||||||
chr4:55981575
|
G | T | 1 | a0002c0002t0003g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1779+196G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55981575 | ||||||
chr4:55981802
|
T | G | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1779+423T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55981802 | ||||||
chr4:55982023
|
T | C | 1 | a0001c0001t0021g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1779+644T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55982023 | ||||||
chr4:55982147
|
C | G | 2 | a0001c0001t0004g0287a0001c0015t0004g0286 | 2 | HG00408.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1779+768C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55982147 | ||||||
chr4:55982203
|
A | G | 1 | a0001c0001t0005g0249 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1779+824A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55982203 | ||||||
chr4:55982313
|
A | G | 1 | a0001c0001t0001g0253 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1779+934A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55982313 | ||||||
chr4:55982340
|
A | G | 3 | a0001c0001t0002g0105a0007c0009t0002g0095a0007c0009t0002g0115 | 3 | HG00140.hp1 HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1779+961A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55982340 | ||||||
chr4:55982426
|
A | G | 1 | a0001c0001t0005g0248 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1779+1047A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55982426 | ||||||
chr4:55982510
|
G | A | 1 | a0001c0001t0022g0116 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1779+1131G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55982510 | ||||||
chr4:55982847
|
C | A | 1 | a0009c0018t0018g0271 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1779+1468C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55982847 | ||||||
chr4:55983149
|
T | C | 1 | a0002c0002t0017g0308 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1779+1770T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983149 | ||||||
chr4:55983218
|
A | G | 1 | a0001c0001t0004g0300 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1779+1839A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983218 | ||||||
chr4:55983324
|
C | T | 9 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(6): Show | 9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1779+1945C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983324 | ||||||
chr4:55983453
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1780-1828C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983453 | ||||||
chr4:55983628
|
A | G | 1 | a0001c0001t0002g0030 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1780-1653A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983628 | ||||||
chr4:55983638
|
CT | C | 141 | a0001c0001t0001g0176a0001c0001t0002g0005a0001c0001t0002g0008others(138): Show | 151 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1780-1630delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr4 | 55983638 | |||||
chr4:55983651
|
T | G | 50 | a0001c0001t0013g0269a0001c0001t0013g0270a0001c0001t0019g0280others(47): Show | 56 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1780-1630T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983651 | ||||||
chr4:55983666
|
C | T | 2 | a0001c0001t0014g0032a0001c0001t0014g0033 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1780-1615C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983666 | ||||||
chr4:55983706
|
A | G | 6 | a0001c0001t0007g0004a0001c0001t0007g0027a0001c0001t0011g0025others(3): Show | 8 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1780-1575A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983706 | ||||||
chr4:55983734
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0211 | 2 | HG01069.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1780-1547C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983734 | ||||||
chr4:55983807
|
A | G | 1 | a0001c0001t0013g0270 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1780-1474A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983807 | ||||||
chr4:55983811
|
T | C | 45 | a0001c0001t0031g0131a0002c0002t0003g0002a0002c0002t0003g0012others(42): Show | 51 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1780-1470T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983811 | ||||||
chr4:55983826
|
A | T | 1 | a0002c0002t0003g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1780-1455A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983826 | ||||||
chr4:55984032
|
A | G | 45 | a0001c0001t0031g0131a0002c0002t0003g0002a0002c0002t0003g0012others(42): Show | 51 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1780-1249A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984032 | ||||||
chr4:55984153
|
G | A | 9 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(6): Show | 9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1780-1128G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984153 | ||||||
chr4:55984246
|
A | T | 43 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0030others(40): Show | 45 | HG00423.hp2 HG00609.hp2 HG01346.hp2 others(42): Show |
intron_variant | MODIFIER | c.1780-1035A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984246 | ||||||
chr4:55984546
|
G | T | 191 | a0001c0001t0001g0296a0001c0001t0002g0005a0001c0001t0002g0008others(188): Show | 212 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1780-735G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984546 | ||||||
chr4:55984680
|
A | G | 9 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(6): Show | 9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1780-601A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984680 | ||||||
chr4:55984730
|
A | G | 3 | a0001c0001t0002g0066a0001c0001t0002g0110a0001c0001t0002g0114 | 3 | HG00642.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1780-551A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984730 | ||||||
chr4:55984786
|
C | G | 1 | a0003c0004t0003g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1780-495C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984786 | ||||||
chr4:55984837
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1780-444C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984837 | ||||||
chr4:55984857
|
G | T | 45 | a0001c0001t0031g0131a0002c0002t0003g0002a0002c0002t0003g0012others(42): Show | 51 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1780-424G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984857 | ||||||
chr4:55984872
|
C | T | 1 | a0001c0001t0005g0024 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1780-409C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984872 | ||||||
chr4:55984982
|
G | C | 6 | a0001c0001t0007g0004a0001c0001t0007g0027a0001c0001t0011g0025others(3): Show | 8 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1780-299G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984982 | ||||||
chr4:55984993
|
A | G | 40 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0030others(37): Show | 42 | HG00423.hp2 HG00609.hp2 HG01346.hp2 others(39): Show |
intron_variant | MODIFIER | c.1780-288A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984993 | ||||||
chr4:55985061
|
A | T | 45 | a0001c0001t0031g0131a0002c0002t0003g0002a0002c0002t0003g0012others(42): Show | 51 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1780-220A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55985061 | ||||||
chr4:55985241
|
T | C | 1 | a0001c0001t0014g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1780-40T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55985241 | ||||||
chr4:55985425
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1857+67A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55985425 | ||||||
chr4:55985430
|
CTA | C | 3 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0232 | 3 | HG02615.hp1 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1857+74_1857+75del others(2): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr4 | 55985430 | |||||
chr4:55985558
|
G | A | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1857+200G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55985558 | ||||||
chr4:55985700
|
A | G | 1 | a0001c0001t0002g0081 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1857+342A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55985700 | ||||||
chr4:55986020
|
G | A | 1 | a0001c0001t0002g0105 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1857+662G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55986020 | ||||||
chr4:55986124
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1857+766C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55986124 | ||||||
chr4:55986130
|
G | A | 1 | a0001c0001t0020g0268 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1857+772G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55986130 | ||||||
chr4:55986174
|
A | G | 44 | a0002c0002t0003g0002a0002c0002t0003g0012a0002c0002t0003g0013others(41): Show | 50 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1857+816A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55986174 | ||||||
chr4:55986181
|
C | T | 4 | a0001c0001t0005g0220a0001c0001t0005g0246a0001c0001t0005g0248others(1): Show | 4 | HG00738.hp1 HG01993.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1857+823C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55986181 | ||||||
chr4:55986302
|
C | T | 1 | a0002c0002t0003g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1857+944C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55986302 | ||||||
chr4:55986334
|
G | C | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1857+976G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55986334 | ||||||
chr4:55987043
|
A | G | 83 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(80): Show | 88 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.1857+1685A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55987043 | ||||||
chr4:55987096
|
G | A | 1 | a0001c0001t0004g0301 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1857+1738G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55987096 | ||||||
chr4:55987325
|
G | A | 3 | a0002c0002t0003g0013a0002c0002t0003g0149a0002c0002t0015g0013 | 3 | HG03098.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1857+1967G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55987325 | ||||||
chr4:55987472
|
A | G | 1 | a0001c0001t0002g0086 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1857+2114A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55987472 | ||||||
chr4:55987474
|
A | G | 1 | a0013c0011t0005g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1857+2116A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55987474 | ||||||
chr4:55987591
|
G | A | 189 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(186): Show | 210 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.1857+2233G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55987591 | ||||||
chr4:55987805
|
G | C | 7 | a0001c0001t0007g0004a0001c0001t0007g0027a0001c0001t0011g0025others(4): Show | 9 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1857+2447G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55987805 | ||||||
chr4:55987810
|
G | A | 1 | a0001c0001t0014g0032 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1857+2452G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55987810 | ||||||
chr4:55987919
|
A | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0219 | 2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1857+2561A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55987919 | ||||||
chr4:55988003
|
A | G | 1 | a0001c0001t0007g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1857+2645A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988003 | ||||||
chr4:55988084
|
T | C | 1 | a0002c0002t0017g0308 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1857+2726T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988084 | ||||||
chr4:55988145
|
G | GT | 190 | a0001c0001t0001g0296a0001c0001t0002g0005a0001c0001t0002g0008others(187): Show | 211 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.1857+2788dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr4 | 55988145 | |||||
chr4:55988165
|
T | G | 1 | a0001c0001t0001g0169 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1857+2807T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988165 | ||||||
chr4:55988228
|
G | A | 44 | a0001c0001t0002g0110a0002c0002t0003g0002a0002c0002t0003g0012others(41): Show | 50 | HG00408.hp2 HG00639.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1857+2870G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988228 | ||||||
chr4:55988261
|
C | T | 1 | a0002c0002t0003g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1857+2903C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988261 | ||||||
chr4:55988402
|
G | A | 1 | a0001c0001t0001g0223 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1857+3044G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988402 | ||||||
chr4:55988661
|
G | GA | 120 | a0001c0001t0001g0296a0001c0001t0002g0005a0001c0001t0002g0008others(117): Show | 130 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.1858-3260dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr4 | 55988661 | |||||
chr4:55988661
|
GA | G | 6 | a0001c0001t0001g0179a0001c0001t0001g0191a0001c0001t0001g0202others(3): Show | 6 | HG00741.hp2 HG01516.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1858-3260delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr4 | 55988661 | |||||
chr4:55988687
|
G | T | 1 | a0001c0001t0004g0297 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1858-3247G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988687 | ||||||
chr4:55988753
|
C | T | 1 | a0001c0001t0004g0300 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1858-3181C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988753 | ||||||
chr4:55988773
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1858-3161C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988773 | ||||||
chr4:55988817
|
C | T | 3 | a0001c0001t0007g0004a0001c0001t0007g0027a0001c0016t0027g0278 | 5 | HG02258.hp1 HG02280.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1858-3117C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988817 | ||||||
chr4:55988818
|
G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0211 | 2 | HG01069.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1858-3116G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988818 | ||||||
chr4:55988831
|
G | C | 1 | a0001c0001t0005g0212 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1858-3103G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988831 | ||||||
chr4:55988853
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1858-3081C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988853 | ||||||
chr4:55988894
|
G | A | 1 | a0001c0001t0031g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1858-3040G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988894 | ||||||
chr4:55988935
|
C | T | 1 | a0001c0001t0002g0091 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1858-2999C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988935 | ||||||
chr4:55988966
|
G | GA | 17 | a0001c0001t0002g0096a0001c0001t0002g0111a0001c0001t0002g0188others(14): Show | 17 | HG01243.hp2 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1858-2954dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr4 | 55988966 | |||||
chr4:55988989
|
A | G | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1858-2945A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988989 | ||||||
chr4:55989021
|
C | T | 2 | a0001c0001t0007g0004a0001c0001t0007g0027 | 4 | HG02258.hp1 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1858-2913C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55989021 | ||||||
chr4:55989044
|
G | A | 9 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(6): Show | 9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1858-2890G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55989044 | ||||||
chr4:55989076
|
A | G | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1858-2858A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55989076 | ||||||
chr4:55989349
|
T | G | 4 | a0001c0001t0001g0015a0001c0001t0001g0195a0001c0001t0001g0266others(1): Show | 5 | HG00558.hp1 HG00609.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.1858-2585T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55989349 | ||||||
chr4:55989354
|
T | C | 8 | a0001c0001t0005g0182a0001c0001t0005g0212a0001c0001t0005g0220others(5): Show | 8 | HG00738.hp1 HG01515.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.1858-2580T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55989354 | ||||||
chr4:55989366
|
A | G | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1858-2568A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55989366 | ||||||
chr4:55989447
|
G | A | 5 | a0001c0001t0004g0007a0001c0001t0004g0281a0001c0001t0004g0282others(2): Show | 5 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.1858-2487G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55989447 | ||||||
chr4:55989501
|
A | G | 190 | a0001c0001t0001g0296a0001c0001t0002g0005a0001c0001t0002g0008others(187): Show | 211 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.1858-2433A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55989501 | ||||||
chr4:55989651
|
A | G | 44 | a0002c0002t0003g0002a0002c0002t0003g0012a0002c0002t0003g0013others(41): Show | 50 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1858-2283A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55989651 | ||||||
chr4:55990004
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1858-1930T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990004 | ||||||
chr4:55990053
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1858-1881T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990053 | ||||||
chr4:55990208
|
T | C | 1 | a0001c0001t0020g0268 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1858-1726T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990208 | ||||||
chr4:55990543
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1858-1391C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990543 | ||||||
chr4:55990544
|
G | A | 81 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(78): Show | 86 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.1858-1390G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990544 | ||||||
chr4:55990609
|
C | G | 3 | a0001c0001t0013g0269a0001c0001t0013g0270a0001c0001t0020g0268 | 3 | HG02258.hp2 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1858-1325C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990609 | ||||||
chr4:55990677
|
T | A | 5 | a0001c0001t0001g0123a0001c0001t0001g0179a0001c0001t0001g0255others(2): Show | 5 | NA18970.hp1 NA18977.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.1858-1257T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990677 | ||||||
chr4:55990701
|
C | G | 1 | a0001c0001t0001g0168 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1858-1233C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990701 | ||||||
chr4:55990703
|
G | A | 189 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(186): Show | 210 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.1858-1231G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990703 | ||||||
chr4:55990849
|
G | C | 190 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(187): Show | 211 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.1858-1085G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990849 | ||||||
chr4:55990943
|
T | A | 1 | a0001c0001t0005g0024 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1858-991T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990943 | ||||||
chr4:55990973
|
A | G | 1 | a0001c0001t0004g0285 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1858-961A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990973 | ||||||
chr4:55990980
|
CT | C | 43 | a0001c0001t0001g0226a0001c0001t0004g0007a0001c0001t0004g0020others(40): Show | 46 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1858-941delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr4 | 55990980 | |||||
chr4:55991109
|
A | G | 2 | a0006c0008t0011g0028a0006c0008t0011g0029 | 2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1858-825A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55991109 | ||||||
chr4:55991177
|
C | T | 3 | a0001c0001t0014g0032a0001c0001t0014g0033a0001c0001t0019g0280 | 3 | HG02647.hp2 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1858-757C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55991177 | ||||||
chr4:55991178
|
G | A | 1 | a0001c0001t0004g0287 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1858-756G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55991178 | ||||||
chr4:55991190
|
A | G | 1 | a0001c0001t0004g0295 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1858-744A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55991190 | ||||||
chr4:55991318
|
CT | C | 35 | a0001c0001t0002g0082a0001c0001t0004g0007a0001c0001t0004g0020others(32): Show | 38 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1858-601delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr4 | 55991318 | |||||
chr4:55991324
|
T | C | 1 | a0009c0018t0018g0271 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1858-610T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55991324 | ||||||
chr4:55991409
|
T | A | 1 | a0001c0001t0012g0160 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1858-525T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55991409 | ||||||
chr4:55991436
|
T | C | 1 | a0002c0002t0003g0135 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1858-498T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55991436 | ||||||
chr4:55991841
|
G | C | 82 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(79): Show | 88 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.1858-93G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55991841 | ||||||
chr4:55991921
|
A | G | 1 | a0001c0001t0002g0279 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1858-13A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55991921 | ||||||
chr4:55992169
|
T | G | 6 | a0001c0001t0002g0008a0001c0001t0002g0081a0001c0001t0002g0087others(3): Show | 6 | HG01346.hp2 HG01433.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.2009+84T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992169 | ||||||
chr4:55992284
|
A | G | 47 | a0002c0002t0003g0002a0002c0002t0003g0012a0002c0002t0003g0013others(44): Show | 53 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.2009+199A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992284 | ||||||
chr4:55992448
|
A | G | 1 | a0001c0001t0002g0058 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2009+363A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992448 | ||||||
chr4:55992455
|
T | A | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2009+370T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992455 | ||||||
chr4:55992460
|
T | G | 2 | a0001c0001t0013g0269a0001c0001t0013g0270 | 2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2009+375T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992460 | ||||||
chr4:55992471
|
G | T | 2 | a0001c0001t0013g0269a0001c0001t0013g0270 | 2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2009+386G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992471 | ||||||
chr4:55992535
|
A | G | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2009+450A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992535 | ||||||
chr4:55992658
|
C | T | 2 | a0001c0001t0010g0056a0001c0001t0010g0057 | 2 | HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2009+573C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992658 | ||||||
chr4:55992772
|
C | T | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2009+687C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992772 | ||||||
chr4:55992889
|
G | A | 1 | a0012c0014t0002g0097 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2009+804G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992889 | ||||||
chr4:55992916
|
G | A | 1 | a0001c0001t0004g0303 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2009+831G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992916 | ||||||
chr4:55992932
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0202 | 2 | HG00741.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2009+847C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992932 | ||||||
chr4:55993080
|
A | T | 2 | a0001c0001t0002g0074a0001c0001t0002g0083 | 2 | NA18950.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.2009+995A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55993080 | ||||||
chr4:55993244
|
C | T | 1 | a0001c0001t0022g0116 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2009+1159C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55993244 | ||||||
chr4:55993335
|
T | C | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2009+1250T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55993335 | ||||||
chr4:55993385
|
C | G | 2 | a0001c0001t0013g0269a0001c0001t0013g0270 | 2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2009+1300C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55993385 | ||||||
chr4:55993634
|
A | G | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2009+1549A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55993634 | ||||||
chr4:55993641
|
C | T | 1 | a0002c0002t0003g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2009+1556C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55993641 | ||||||
chr4:55993811
|
G | A | 1 | a0001c0001t0020g0268 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2009+1726G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55993811 | ||||||
chr4:55994135
|
T | C | 10 | a0001c0001t0006g0031a0001c0001t0006g0043a0001c0001t0006g0044others(7): Show | 10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.2009+2050T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994135 | ||||||
chr4:55994587
|
C | T | 10 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(7): Show | 10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2009+2502C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994587 | ||||||
chr4:55994656
|
A | G | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2009+2571A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994656 | ||||||
chr4:55994672
|
A | G | 8 | a0001c0001t0006g0031a0001c0001t0006g0045a0001c0001t0006g0046others(5): Show | 8 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.2009+2587A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994672 | ||||||
chr4:55994686
|
CT | C | 8 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0208others(5): Show | 8 | HG01168.hp1 HG01934.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.2009+2618delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr4 | 55994686 | |||||
chr4:55994718
|
C | T | 81 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(78): Show | 86 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.2009+2633C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994718 | ||||||
chr4:55994846
|
C | T | 1 | a0001c0001t0031g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2009+2761C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994846 | ||||||
chr4:55994849
|
A | G | 6 | a0002c0002t0003g0012a0002c0002t0003g0090a0002c0002t0003g0118others(3): Show | 7 | NA18961.hp2 NA18979.hp1 NA18995.hp1 others(4): Show |
intron_variant | MODIFIER | c.2009+2764A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994849 | ||||||
chr4:55994878
|
G | A | 1 | a0002c0002t0003g0014 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2009+2793G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994878 | ||||||
chr4:55994907
|
A | G | 1 | a0001c0001t0031g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2009+2822A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994907 | ||||||
chr4:55994980
|
T | C | 205 | a0001c0001t0001g0296a0001c0001t0002g0005a0001c0001t0002g0008others(202): Show | 226 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.2009+2895T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994980 | ||||||
chr4:55995142
|
T | A | 1 | a0002c0002t0003g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2009+3057T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55995142 | ||||||
chr4:55995144
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2009+3059C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55995144 | ||||||
chr4:55995307
|
C | T | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2009+3222C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55995307 | ||||||
chr4:55995392
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2009+3307G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55995392 | ||||||
chr4:55995493
|
C | T | 1 | a0001c0001t0031g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2009+3408C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55995493 | ||||||
chr4:55995641
|
A | G | 1 | a0001c0001t0020g0268 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2009+3556A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55995641 | ||||||
chr4:55995706
|
C | T | 1 | a0005c0006t0008g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2010-3596C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55995706 | ||||||
chr4:55995719
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2010-3583C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55995719 | ||||||
chr4:55996714
|
C | CT | 6 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0219others(3): Show | 7 | HG01975.hp2 HG01981.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.2010-2574dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr4 | 55996714 | |||||
chr4:55996922
|
A | G | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2010-2380A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55996922 | ||||||
chr4:55996952
|
A | T | 2 | a0001c0001t0007g0004a0001c0001t0007g0027 | 4 | HG02258.hp1 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2010-2350A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55996952 | ||||||
chr4:55997045
|
C | G | 1 | a0008c0010t0001g0231 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2010-2257C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55997045 | ||||||
chr4:55997054
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2010-2248G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55997054 | ||||||
chr4:55997173
|
T | G | 1 | a0001c0001t0001g0226 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2010-2129T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55997173 | ||||||
chr4:55997696
|
G | GT | 203 | a0001c0001t0001g0296a0001c0001t0002g0005a0001c0001t0002g0008others(200): Show | 224 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.2010-1599dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr4 | 55997696 | |||||
chr4:55997747
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2010-1555G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55997747 | ||||||
chr4:55997775
|
A | C | 2 | a0001c0001t0019g0280a0001c0001t0031g0131 | 2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2010-1527A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55997775 | ||||||
chr4:55997848
|
A | G | 1 | a0002c0002t0003g0235 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2010-1454A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55997848 | ||||||
chr4:55997866
|
A | G | 57 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(54): Show | 63 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.2010-1436A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55997866 | ||||||
chr4:55997868
|
T | G | 10 | a0001c0001t0006g0031a0001c0001t0006g0043a0001c0001t0006g0044others(7): Show | 10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.2010-1434T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55997868 | ||||||
chr4:55998033
|
G | A | 1 | a0001c0001t0024g0307 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2010-1269G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55998033 | ||||||
chr4:55998115
|
G | A | 1 | a0001c0001t0012g0160 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2010-1187G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55998115 | ||||||
chr4:55998148
|
G | A | 1 | a0002c0002t0003g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2010-1154G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55998148 | ||||||
chr4:55998211
|
A | G | 1 | a0001c0001t0021g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2010-1091A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55998211 | ||||||
chr4:55998335
|
A | G | 115 | a0001c0001t0001g0296a0001c0001t0002g0005a0001c0001t0002g0008others(112): Show | 123 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.2010-967A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55998335 | ||||||
chr4:55998457
|
CT | C | 3 | a0001c0001t0014g0032a0001c0001t0014g0033a0001c0016t0027g0278 | 3 | HG02717.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2010-841delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr4 | 55998457 | |||||
chr4:55998597
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2010-705G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55998597 | ||||||
chr4:55998794
|
G | C | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2010-508G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55998794 | ||||||
chr4:55998880
|
A | G | 17 | a0001c0001t0002g0030a0001c0001t0002g0037a0001c0001t0002g0038others(14): Show | 17 | HG00423.hp2 HG03654.hp1 HG03704.hp1 others(14): Show |
intron_variant | MODIFIER | c.2010-422A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55998880 | ||||||
chr4:55998971
|
C | A | 38 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(35): Show | 41 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.2010-331C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55998971 | ||||||
chr4:55999139
|
A | G | 2 | a0001c0001t0002g0071a0001c0001t0002g0073 | 2 | HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2010-163A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55999139 | ||||||
chr4:55999146
|
T | C | 1 | a0002c0002t0003g0136 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2010-156T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55999146 | ||||||
chr4:55999157
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2010-145A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55999157 | ||||||
chr4:55999194
|
C | A | 10 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(7): Show | 10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2010-108C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55999194 | ||||||
chr4:55999855
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2280+210G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 55999855 | ||||||
chr4:55999897
|
T | A | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2280+252T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 55999897 | ||||||
chr4:55999997
|
C | T | 10 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(7): Show | 10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2280+352C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 55999997 | ||||||
chr4:56000132
|
C | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2280+487C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000132 | ||||||
chr4:56000316
|
C | T | 1 | a0001c0016t0027g0278 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2280+671C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000316 | ||||||
chr4:56000343
|
A | G | 2 | a0001c0001t0019g0280a0001c0001t0031g0131 | 2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2280+698A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000343 | ||||||
chr4:56000415
|
A | G | 1 | a0001c0001t0004g0303 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2280+770A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000415 | ||||||
chr4:56000664
|
G | A | 2 | a0001c0001t0010g0056a0001c0001t0010g0057 | 2 | HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2280+1019G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000664 | ||||||
chr4:56000704
|
T | C | 1 | a0001c0001t0021g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2280+1059T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000704 | ||||||
chr4:56000714
|
G | A | 1 | a0001c0001t0021g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2280+1069G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000714 | ||||||
chr4:56000804
|
T | C | 1 | a0013c0011t0005g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2280+1159T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000804 | ||||||
chr4:56000820
|
C | A | 1 | a0001c0001t0001g0172 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2280+1175C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000820 | ||||||
chr4:56000921
|
C | A | 8 | a0002c0002t0003g0034a0002c0002t0003g0132a0002c0002t0003g0148others(5): Show | 8 | HG01099.hp2 HG01106.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.2280+1276C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000921 | ||||||
chr4:56001040
|
T | C | 1 | a0001c0001t0002g0100 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2280+1395T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56001040 | ||||||
chr4:56001760
|
A | AT | 204 | a0001c0001t0001g0296a0001c0001t0002g0005a0001c0001t0002g0008others(201): Show | 225 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.2280+2124dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr4 | 56001760 | |||||
chr4:56001863
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2280+2218T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56001863 | ||||||
chr4:56002049
|
G | T | 1 | a0001c0001t0024g0307 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2280+2404G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56002049 | ||||||
chr4:56002053
|
G | C | 42 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0030others(39): Show | 44 | HG00423.hp2 HG00609.hp2 HG01346.hp2 others(41): Show |
intron_variant | MODIFIER | c.2280+2408G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56002053 | ||||||
chr4:56002176
|
A | G | 80 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(77): Show | 85 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.2280+2531A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56002176 | ||||||
chr4:56002386
|
C | T | 204 | a0001c0001t0001g0296a0001c0001t0002g0005a0001c0001t0002g0008others(201): Show | 225 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.2280+2741C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56002386 | ||||||
chr4:56002479
|
A | G | 1 | a0001c0001t0005g0218 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2280+2834A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56002479 | ||||||
chr4:56003051
|
T | C | 87 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(84): Show | 94 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.2280+3406T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003051 | ||||||
chr4:56003122
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2280+3477A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003122 | ||||||
chr4:56003123
|
C | T | 1 | a0013c0011t0005g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2280+3478C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003123 | ||||||
chr4:56003165
|
A | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0259 | 3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2280+3520A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003165 | ||||||
chr4:56003273
|
C | T | 4 | a0001c0001t0002g0061a0001c0001t0002g0078a0001c0001t0002g0080others(1): Show | 4 | NA18975.hp2 NA19062.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.2280+3628C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003273 | ||||||
chr4:56003320
|
C | T | 2 | a0001c0001t0010g0056a0001c0001t0010g0057 | 2 | HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2280+3675C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003320 | ||||||
chr4:56003353
|
C | G | 1 | a0001c0001t0006g0047 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2280+3708C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003353 | ||||||
chr4:56003459
|
C | T | 47 | a0002c0002t0003g0002a0002c0002t0003g0012a0002c0002t0003g0013others(44): Show | 53 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.2280+3814C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003459 | ||||||
chr4:56003460
|
G | A | 1 | a0001c0001t0004g0277 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2280+3815G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003460 | ||||||
chr4:56003468
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2280+3823A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003468 | ||||||
chr4:56003584
|
A | G | 254 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0166others(251): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.2280+3939A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003584 | ||||||
chr4:56003659
|
G | A | 1 | a0001c0001t0001g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2280+4014G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003659 | ||||||
chr4:56003670
|
A | G | 4 | a0002c0002t0003g0034a0002c0002t0003g0162a0002c0002t0003g0163others(1): Show | 4 | HG01099.hp2 HG01192.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.2280+4025A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003670 | ||||||
chr4:56003720
|
TG | T | 3 | a0001c0001t0004g0293a0001c0001t0004g0294a0001c0001t0004g0295 | 3 | HG02280.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2280+4076delG | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003720 | ||||||
chr4:56003726
|
T | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0195 | 3 | HG00558.hp1 HG00609.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.2280+4081T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003726 | ||||||
chr4:56003729
|
T | C | 1 | a0002c0002t0003g0034 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2280+4084T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003729 | ||||||
chr4:56003780
|
G | A | 1 | a0013c0011t0005g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2280+4135G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003780 | ||||||
chr4:56003909
|
C | T | 1 | a0002c0002t0003g0162 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2280+4264C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003909 | ||||||
chr4:56004179
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0202 | 2 | HG00741.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2281-4148G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56004179 | ||||||
chr4:56004289
|
A | G | 1 | a0001c0001t0002g0037 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2281-4038A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56004289 | ||||||
chr4:56004479
|
A | T | 36 | a0001c0001t0001g0296a0001c0001t0004g0007a0001c0001t0004g0020others(33): Show | 39 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.2281-3848A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56004479 | ||||||
chr4:56004625
|
C | A | 1 | a0002c0002t0003g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2281-3702C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56004625 | ||||||
chr4:56004678
|
A | G | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2281-3649A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56004678 | ||||||
chr4:56004926
|
A | AT | 98 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0186others(95): Show | 105 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2281-3383dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr4 | 56004926 | |||||
chr4:56004926
|
A | ATT | 16 | a0001c0001t0002g0005a0001c0001t0002g0061a0001c0001t0002g0068others(13): Show | 18 | HG01175.hp2 HG01928.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.2281-3384_2281-338 others(6): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr4 | 56004926 | |||||
chr4:56004926
|
A | T | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2281-3401A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56004926 | ||||||
chr4:56004926
|
AT | A | 14 | a0001c0001t0001g0195a0001c0001t0001g0259a0001c0001t0005g0254others(11): Show | 14 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(11): Show |
intron_variant | MODIFIER | c.2281-3383delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr4 | 56004926 | |||||
chr4:56004926
|
ATT | A | 11 | a0001c0001t0031g0131a0001c0003t0003g0003a0001c0003t0003g0019others(8): Show | 17 | HG00558.hp2 HG00639.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.2281-3384_2281-338 others(6): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr4 | 56004926 | |||||
chr4:56004926
|
ATTT | A | 53 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(50): Show | 58 | HG00408.hp2 HG00738.hp2 HG01099.hp2 others(55): Show |
intron_variant | MODIFIER | c.2281-3385_2281-338 others(7): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr4 | 56004926 | |||||
chr4:56005216
|
C | G | 203 | a0001c0001t0001g0296a0001c0001t0002g0005a0001c0001t0002g0008others(200): Show | 224 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.2281-3111C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56005216 | ||||||
chr4:56005391
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2281-2936C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56005391 | ||||||
chr4:56005397
|
G | A | 38 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(35): Show | 41 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.2281-2930G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56005397 | ||||||
chr4:56005514
|
G | T | 1 | a0001c0001t0002g0113 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2281-2813G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56005514 | ||||||
chr4:56005722
|
G | A | 76 | a0001c0001t0006g0031a0001c0001t0006g0043a0001c0001t0006g0044others(73): Show | 87 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.2281-2605G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56005722 | ||||||
chr4:56005739
|
A | G | 1 | a0001c0001t0004g0277 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2281-2588A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56005739 | ||||||
chr4:56005758
|
G | A | 1 | a0001c0001t0031g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2281-2569G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56005758 | ||||||
chr4:56005873
|
A | G | 1 | a0001c0001t0021g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2281-2454A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56005873 | ||||||
chr4:56005926
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2281-2401C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56005926 | ||||||
chr4:56006362
|
T | C | 7 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0208others(4): Show | 7 | HG02132.hp2 HG02735.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.2281-1965T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006362 | ||||||
chr4:56006450
|
T | C | 2 | a0001c0001t0004g0288a0001c0001t0004g0291 | 2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2281-1877T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006450 | ||||||
chr4:56006500
|
C | T | 3 | a0001c0001t0004g0293a0001c0001t0004g0294a0001c0001t0004g0295 | 3 | HG02280.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2281-1827C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006500 | ||||||
chr4:56006503
|
A | G | 88 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(85): Show | 95 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2281-1824A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006503 | ||||||
chr4:56006533
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2281-1794G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006533 | ||||||
chr4:56006629
|
T | A | 1 | a0001c0001t0002g0076 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2281-1698T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006629 | ||||||
chr4:56006718
|
G | A | 1 | a0001c0001t0031g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2281-1609G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006718 | ||||||
chr4:56006791
|
A | G | 47 | a0002c0002t0003g0002a0002c0002t0003g0012a0002c0002t0003g0013others(44): Show | 53 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.2281-1536A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006791 | ||||||
chr4:56006862
|
G | T | 1 | a0013c0011t0005g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2281-1465G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006862 | ||||||
chr4:56006926
|
C | T | 10 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(7): Show | 10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2281-1401C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006926 | ||||||
chr4:56006985
|
C | A | 1 | a0001c0001t0001g0260 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2281-1342C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006985 | ||||||
chr4:56007050
|
C | T | 1 | a0001c0001t0002g0103 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2281-1277C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007050 | ||||||
chr4:56007075
|
G | A | 1 | a0001c0001t0006g0047 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2281-1252G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007075 | ||||||
chr4:56007077
|
A | C | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2281-1250A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007077 | ||||||
chr4:56007124
|
TCTCAGGT others(11): Show |
T | 1 | a0002c0002t0003g0128 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2281-1197_2281-118 others(22): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr4 | 56007124 | |||||
chr4:56007292
|
T | C | 1 | a0001c0001t0001g0222 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2281-1035T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007292 | ||||||
chr4:56007446
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2281-881C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007446 | ||||||
chr4:56007528
|
G | A | 2 | a0001c0001t0004g0281a0001c0001t0004g0282 | 2 | HG00735.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.2281-799G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007528 | ||||||
chr4:56007678
|
A | G | 10 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(7): Show | 10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2281-649A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007678 | ||||||
chr4:56007748
|
G | C | 1 | a0001c0016t0027g0278 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2281-579G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007748 | ||||||
chr4:56007790
|
T | C | 204 | a0001c0001t0001g0296a0001c0001t0002g0005a0001c0001t0002g0008others(201): Show | 225 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.2281-537T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007790 | ||||||
chr4:56007808
|
T | C | 1 | a0002c0002t0003g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2281-519T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007808 | ||||||
chr4:56007888
|
T | C | 7 | a0001c0001t0007g0004a0001c0001t0007g0027a0001c0001t0007g0053others(4): Show | 9 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2281-439T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007888 | ||||||
chr4:56007907
|
T | C | 12 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0002g0023others(9): Show | 14 | HG02132.hp1 NA18956.hp2 NA18957.hp1 others(11): Show |
intron_variant | MODIFIER | c.2281-420T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007907 | ||||||
chr4:56007914
|
G | A | 1 | a0001c0001t0024g0307 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2281-413G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007914 | ||||||
chr4:56007941
|
C | T | 10 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(7): Show | 10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2281-386C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007941 | ||||||
chr4:56008076
|
G | A | 76 | a0001c0001t0006g0031a0001c0001t0006g0043a0001c0001t0006g0044others(73): Show | 87 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.2281-251G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56008076 | ||||||
chr4:56008115
|
G | C | 1 | a0001c0001t0001g0262 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2281-212G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56008115 | ||||||
chr4:56008435
|
C | T | 2 | a0001c0001t0020g0268a0001c0001t0031g0131 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2336+53C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56008435 | ||||||
chr4:56008485
|
A | G | 3 | a0001c0001t0014g0032a0001c0001t0014g0033a0001c0016t0027g0278 | 3 | HG02717.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2336+103A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56008485 | ||||||
chr4:56008612
|
A | G | 1 | a0001c0001t0005g0245 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2336+230A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56008612 | ||||||
chr4:56008767
|
T | C | 1 | a0002c0002t0003g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2336+385T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56008767 | ||||||
chr4:56008844
|
A | G | 1 | a0001c0001t0001g0221 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2336+462A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56008844 | ||||||
chr4:56009045
|
T | C | 42 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0030others(39): Show | 44 | HG00423.hp2 HG00609.hp2 HG01346.hp2 others(41): Show |
intron_variant | MODIFIER | c.2336+663T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009045 | ||||||
chr4:56009091
|
A | G | 203 | a0001c0001t0001g0296a0001c0001t0002g0005a0001c0001t0002g0008others(200): Show | 224 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.2337-644A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009091 | ||||||
chr4:56009155
|
G | T | 199 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(196): Show | 220 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.2337-580G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009155 | ||||||
chr4:56009158
|
G | T | 3 | a0001c0001t0002g0272a0001c0001t0004g0292a0001c0001t0006g0050 | 3 | HG03130.hp1 HG03710.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.2337-577G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009158 | ||||||
chr4:56009167
|
G | T | 255 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0166others(252): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.2337-568G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009167 | ||||||
chr4:56009198
|
G | A | 1 | a0001c0001t0021g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2337-537G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009198 | ||||||
chr4:56009223
|
G | A | 1 | a0001c0001t0006g0045 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2337-512G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009223 | ||||||
chr4:56009225
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0192 | 2 | NA19076.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2337-510G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009225 | ||||||
chr4:56009246
|
C | T | 1 | a0002c0002t0003g0139 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2337-489C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009246 | ||||||
chr4:56009303
|
C | G | 89 | a0001c0001t0006g0031a0001c0001t0006g0043a0001c0001t0006g0044others(86): Show | 102 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.2337-432C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009303 | ||||||
chr4:56009338
|
A | G | 1 | a0002c0002t0003g0130 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2337-397A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009338 | ||||||
chr4:56009641
|
G | A | 1 | a0001c0001t0021g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2337-94G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009641 | ||||||
chr4:56009663
|
A | G | 33 | a0001c0001t0001g0296a0001c0001t0004g0007a0001c0001t0004g0020others(30): Show | 36 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.2337-72A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009663 | ||||||
chr4:56010075
|
C | T | 16 | a0001c0001t0004g0300a0001c0001t0006g0031a0001c0001t0006g0043others(13): Show | 21 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.2505+172C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010075 | ||||||
chr4:56010175
|
AC | A | 58 | a0001c0001t0001g0201a0001c0001t0002g0009a0001c0001t0002g0010others(55): Show | 66 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.2505+282delC | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr4 | 56010175 | |||||
chr4:56010175
|
ACC | A | 149 | a0001c0001t0001g0173a0001c0001t0001g0197a0001c0001t0002g0005others(146): Show | 162 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.2505+281_2505+282d others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr4 | 56010175 | |||||
chr4:56010176
|
C | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0192 | 2 | NA19076.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2505+273C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010176 | ||||||
chr4:56010178
|
C | G | 1 | a0001c0001t0005g0218 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2505+275C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010178 | ||||||
chr4:56010179
|
C | G | 1 | a0001c0001t0005g0243 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2505+276C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010179 | ||||||
chr4:56010179
|
C | T | 1 | a0001c0001t0031g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2505+276C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010179 | ||||||
chr4:56010246
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2505+343C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010246 | ||||||
chr4:56010310
|
C | T | 2 | a0001c0001t0019g0280a0001c0001t0031g0131 | 2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2505+407C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010310 | ||||||
chr4:56010311
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0020g0268 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2505+408G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010311 | ||||||
chr4:56010360
|
CA | C | 192 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(189): Show | 208 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.2505+475delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr4 | 56010360 | |||||
chr4:56010362
|
A | C | 10 | a0001c0001t0002g0105a0001c0001t0006g0031a0001c0001t0006g0043others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(7): Show |
intron_variant | MODIFIER | c.2505+459A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010362 | ||||||
chr4:56010410
|
AAACACAT others(18): Show |
A | 1 | a0001c0001t0020g0268 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2505+509_2505+533d others(27): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr4 | 56010410 | |||||
chr4:56010495
|
A | G | 1 | a0001c0001t0005g0126 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2505+592A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010495 | ||||||
chr4:56010624
|
A | T | 1 | a0001c0001t0002g0083 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2505+721A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010624 | ||||||
chr4:56010697
|
T | C | 2 | a0001c0001t0004g0288a0001c0001t0004g0291 | 2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2506-715T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010697 | ||||||
chr4:56010712
|
C | T | 1 | a0001c0001t0004g0306 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2506-700C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010712 | ||||||
chr4:56011125
|
C | T | 1 | a0001c0001t0004g0288 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2506-287C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56011125 | ||||||
chr4:56011157
|
C | G | 4 | a0001c0001t0001g0179a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | NA18970.hp1 NA18979.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.2506-255C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56011157 | ||||||
chr4:56011300
|
C | G | 5 | a0001c0001t0004g0020a0001c0001t0004g0298a0001c0001t0004g0299others(2): Show | 6 | NA18961.hp1 NA18977.hp2 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.2506-112C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56011300 | ||||||
chr4:56011559
|
G | T | 10 | a0001c0001t0006g0031a0001c0001t0006g0043a0001c0001t0006g0044others(7): Show | 10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.2616+37G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 20/25 | chr4 | 56011559 | ||||||
chr4:56011559
|
GT | G | 31 | a0001c0001t0002g0081a0001c0001t0004g0007a0001c0001t0004g0020others(28): Show | 34 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.2616+51delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr4 | 56011559 | |||||
chr4:56011688
|
A | G | 1 | a0001c0016t0027g0278 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2617-112A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 20/25 | chr4 | 56011688 | ||||||
chr4:56012027
|
A | G | 48 | a0001c0001t0003g0187a0002c0002t0003g0002a0002c0002t0003g0012others(45): Show | 54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.2802+42A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012027 | ||||||
chr4:56012067
|
A | T | 3 | a0001c0001t0001g0258a0007c0009t0002g0095a0007c0009t0002g0115 | 3 | HG01358.hp2 HG01361.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2802+82A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012067 | ||||||
chr4:56012071
|
T | A | 1 | a0001c0001t0001g0253 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2802+86T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012071 | ||||||
chr4:56012088
|
G | T | 1 | a0013c0011t0005g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2802+103G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012088 | ||||||
chr4:56012275
|
C | T | 1 | a0001c0001t0021g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2802+290C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012275 | ||||||
chr4:56012298
|
C | T | 48 | a0001c0001t0003g0187a0002c0002t0003g0002a0002c0002t0003g0012others(45): Show | 54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.2802+313C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012298 | ||||||
chr4:56012424
|
A | G | 1 | a0002c0002t0003g0235 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2802+439A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012424 | ||||||
chr4:56012505
|
T | A | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2802+520T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012505 | ||||||
chr4:56012596
|
G | A | 1 | a0002c0002t0003g0134 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2802+611G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012596 | ||||||
chr4:56012634
|
GT | G | 10 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(7): Show | 10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2802+652delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr4 | 56012634 | |||||
chr4:56012758
|
G | A | 1 | a0001c0001t0005g0212 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2802+773G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012758 | ||||||
chr4:56012989
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2802+1004T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012989 | ||||||
chr4:56013039
|
A | G | 2 | a0001c0003t0003g0273a0001c0003t0003g0274 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2802+1054A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013039 | ||||||
chr4:56013047
|
G | T | 10 | a0001c0001t0006g0031a0001c0001t0006g0043a0001c0001t0006g0044others(7): Show | 10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.2802+1062G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013047 | ||||||
chr4:56013082
|
C | T | 3 | a0002c0002t0003g0013a0002c0002t0003g0149a0002c0002t0015g0013 | 3 | HG03098.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2802+1097C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013082 | ||||||
chr4:56013300
|
C | T | 204 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(201): Show | 225 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.2802+1315C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013300 | ||||||
chr4:56013383
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2802+1398G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013383 | ||||||
chr4:56013494
|
A | G | 48 | a0001c0001t0003g0187a0002c0002t0003g0002a0002c0002t0003g0012others(45): Show | 54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.2802+1509A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013494 | ||||||
chr4:56013543
|
T | G | 5 | a0001c0001t0002g0009a0001c0001t0002g0023a0001c0001t0002g0093others(2): Show | 6 | HG02132.hp1 NA18984.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.2802+1558T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013543 | ||||||
chr4:56013697
|
C | T | 1 | a0013c0011t0005g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2802+1712C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013697 | ||||||
chr4:56013965
|
A | G | 1 | a0009c0018t0018g0271 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2802+1980A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013965 | ||||||
chr4:56013966
|
C | T | 48 | a0001c0001t0003g0187a0002c0002t0003g0002a0002c0002t0003g0012others(45): Show | 54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.2802+1981C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013966 | ||||||
chr4:56014023
|
A | G | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2802+2038A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014023 | ||||||
chr4:56014100
|
T | C | 1 | a0001c0001t0004g0304 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2802+2115T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014100 | ||||||
chr4:56014133
|
C | T | 2 | a0001c0001t0001g0184a0001c0001t0001g0267 | 2 | HG01884.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.2802+2148C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014133 | ||||||
chr4:56014177
|
T | A | 33 | a0001c0001t0001g0296a0001c0001t0004g0007a0001c0001t0004g0020others(30): Show | 36 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.2802+2192T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014177 | ||||||
chr4:56014246
|
A | G | 1 | a0002c0002t0003g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2802+2261A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014246 | ||||||
chr4:56014250
|
CAAACACC others(3): Show |
C | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2802+2269_2802+227 others(14): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr4 | 56014250 | |||||
chr4:56014611
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2802+2626A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014611 | ||||||
chr4:56014646
|
A | G | 10 | a0001c0001t0006g0031a0001c0001t0006g0043a0001c0001t0006g0044others(7): Show | 10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.2802+2661A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014646 | ||||||
chr4:56014708
|
A | G | 1 | a0001c0001t0001g0256 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2802+2723A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014708 | ||||||
chr4:56014736
|
G | A | 5 | a0002c0002t0003g0042a0002c0002t0003g0130a0002c0002t0003g0135others(2): Show | 7 | HG00738.hp2 HG02055.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.2802+2751G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014736 | ||||||
chr4:56014822
|
A | C | 7 | a0001c0001t0007g0004a0001c0001t0007g0027a0001c0001t0007g0053others(4): Show | 9 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2803-2826A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014822 | ||||||
chr4:56014857
|
A | C | 87 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(84): Show | 94 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.2803-2791A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014857 | ||||||
chr4:56014878
|
G | T | 1 | a0001c0001t0005g0249 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2803-2770G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014878 | ||||||
chr4:56014986
|
G | A | 48 | a0001c0001t0003g0187a0002c0002t0003g0002a0002c0002t0003g0012others(45): Show | 54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.2803-2662G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014986 | ||||||
chr4:56015042
|
A | C | 10 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(7): Show | 10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2803-2606A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56015042 | ||||||
chr4:56015052
|
A | G | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2803-2596A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56015052 | ||||||
chr4:56015116
|
C | T | 204 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(201): Show | 225 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.2803-2532C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56015116 | ||||||
chr4:56015169
|
A | T | 1 | a0001c0001t0005g0248 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2803-2479A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56015169 | ||||||
chr4:56015185
|
C | T | 10 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(7): Show | 10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2803-2463C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56015185 | ||||||
chr4:56015459
|
G | A | 1 | a0002c0002t0006g0150 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2803-2189G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56015459 | ||||||
chr4:56015528
|
G | C | 5 | a0001c0001t0004g0007a0001c0001t0004g0281a0001c0001t0004g0282others(2): Show | 5 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.2803-2120G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56015528 | ||||||
chr4:56015558
|
A | G | 2 | a0001c0001t0013g0269a0001c0001t0013g0270 | 2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2803-2090A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56015558 | ||||||
chr4:56016151
|
G | C | 203 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(200): Show | 224 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.2803-1497G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56016151 | ||||||
chr4:56016514
|
G | A | 1 | a0002c0002t0003g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2803-1134G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56016514 | ||||||
chr4:56016577
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2803-1071G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56016577 | ||||||
chr4:56016666
|
A | G | 1 | a0003c0004t0003g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2803-982A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56016666 | ||||||
chr4:56016709
|
A | G | 4 | a0001c0001t0001g0172a0001c0001t0001g0201a0001c0001t0001g0215others(1): Show | 4 | NA19001.hp2 NA19009.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.2803-939A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56016709 | ||||||
chr4:56016888
|
G | A | 1 | a0001c0001t0011g0026 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2803-760G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56016888 | ||||||
chr4:56017094
|
G | T | 1 | a0001c0001t0002g0088 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2803-554G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56017094 | ||||||
chr4:56017204
|
G | A | 4 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(1): Show | 4 | HG01255.hp1 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.2803-444G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56017204 | ||||||
chr4:56017591
|
G | A | 4 | a0001c0001t0002g0069a0001c0001t0002g0077a0001c0001t0002g0089others(1): Show | 4 | HG00609.hp2 HG01934.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.2803-57G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56017591 | ||||||
chr4:56017913
|
T | C | 48 | a0001c0001t0003g0187a0002c0002t0003g0002a0002c0002t0003g0012others(45): Show | 54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.3012+56T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56017913 | ||||||
chr4:56017959
|
G | A | 1 | a0001c0001t0011g0025 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3012+102G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56017959 | ||||||
chr4:56018050
|
G | A | 1 | a0001c0001t0005g0248 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3012+193G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018050 | ||||||
chr4:56018068
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3012+211A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018068 | ||||||
chr4:56018166
|
G | A | 32 | a0001c0001t0004g0007a0001c0001t0004g0020a0001c0001t0004g0021others(29): Show | 35 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.3012+309G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018166 | ||||||
chr4:56018243
|
G | T | 4 | a0001c0001t0011g0025a0001c0001t0011g0026a0006c0008t0011g0028others(1): Show | 4 | HG01243.hp2 HG02300.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3012+386G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018243 | ||||||
chr4:56018249
|
G | A | 1 | a0001c0001t0011g0026 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3012+392G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018249 | ||||||
chr4:56018283
|
A | G | 204 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(201): Show | 225 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.3012+426A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018283 | ||||||
chr4:56018340
|
A | T | 14 | a0001c0001t0001g0018a0001c0001t0001g0040a0001c0001t0001g0171others(11): Show | 15 | HG00423.hp1 HG01069.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.3012+483A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018340 | ||||||
chr4:56018438
|
C | G | 2 | a0001c0001t0013g0269a0001c0001t0013g0270 | 2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3012+581C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018438 | ||||||
chr4:56018524
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3012+667G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018524 | ||||||
chr4:56018664
|
A | G | 203 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(200): Show | 224 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.3013-689A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018664 | ||||||
chr4:56018692
|
C | A | 1 | a0001c0001t0031g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3013-661C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018692 | ||||||
chr4:56018759
|
C | CA | 7 | a0001c0001t0007g0004a0001c0001t0007g0027a0001c0001t0007g0053others(4): Show | 9 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.3013-583dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr4 | 56018759 | |||||
chr4:56019082
|
C | A | 48 | a0001c0001t0003g0187a0002c0002t0003g0002a0002c0002t0003g0012others(45): Show | 54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.3013-271C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56019082 | ||||||
chr4:56019588
|
A | G | 3 | a0002c0002t0003g0013a0002c0002t0003g0149a0002c0002t0015g0013 | 3 | HG03098.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3215+33A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019588 | ||||||
chr4:56019720
|
G | C | 10 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(7): Show | 10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.3215+165G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019720 | ||||||
chr4:56019798
|
G | A | 1 | a0001c0001t0031g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3215+243G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019798 | ||||||
chr4:56019800
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3215+245G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019800 | ||||||
chr4:56019809
|
C | T | 1 | a0001c0001t0031g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3215+254C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019809 | ||||||
chr4:56019844
|
C | A | 2 | a0001c0001t0004g0288a0001c0001t0004g0291 | 2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3215+289C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019844 | ||||||
chr4:56019845
|
G | A | 11 | a0001c0001t0001g0203a0001c0001t0006g0031a0001c0001t0006g0043others(8): Show | 11 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.3215+290G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019845 | ||||||
chr4:56019909
|
A | T | 80 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(77): Show | 85 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.3215+354A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019909 | ||||||
chr4:56019931
|
G | A | 1 | a0001c0001t0009g0213 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3215+376G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019931 | ||||||
chr4:56019996
|
C | T | 17 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0186others(14): Show | 18 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.3215+441C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019996 | ||||||
chr4:56019997
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3215+442G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019997 | ||||||
chr4:56020142
|
G | A | 203 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(200): Show | 224 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.3216-534G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56020142 | ||||||
chr4:56020290
|
T | C | 1 | a0001c0001t0031g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3216-386T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56020290 | ||||||
chr4:56020530
|
A | G | 1 | a0003c0004t0003g0141 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3216-146A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56020530 | ||||||
chr4:56020614
|
C | T | 13 | a0001c0001t0002g0010a0001c0001t0002g0062a0001c0001t0002g0064others(10): Show | 14 | HG00673.hp2 HG02080.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.3216-62C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56020614 | ||||||
chr4:56020846
|
T | C | 4 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(1): Show | 4 | HG01255.hp1 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.3320+66T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56020846 | ||||||
chr4:56020976
|
G | A | 10 | a0001c0001t0006g0031a0001c0001t0006g0043a0001c0001t0006g0044others(7): Show | 10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.3320+196G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56020976 | ||||||
chr4:56021028
|
A | C | 48 | a0001c0001t0003g0187a0002c0002t0003g0002a0002c0002t0003g0012others(45): Show | 54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.3320+248A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56021028 | ||||||
chr4:56021088
|
G | A | 1 | a0001c0001t0004g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3320+308G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56021088 | ||||||
chr4:56021453
|
G | A | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3320+673G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56021453 | ||||||
chr4:56021534
|
C | T | 1 | a0001c0001t0010g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3320+754C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56021534 | ||||||
chr4:56021763
|
G | A | 2 | a0001c0001t0002g0066a0001c0001t0002g0114 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3320+983G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56021763 | ||||||
chr4:56022060
|
G | A | 32 | a0001c0001t0004g0007a0001c0001t0004g0020a0001c0001t0004g0021others(29): Show | 35 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.3320+1280G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56022060 | ||||||
chr4:56022272
|
G | A | 1 | a0001c0001t0004g0293 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3320+1492G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56022272 | ||||||
chr4:56022389
|
G | T | 1 | a0001c0001t0006g0049 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.3320+1609G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56022389 | ||||||
chr4:56022622
|
G | A | 3 | a0002c0002t0003g0014a0002c0002t0003g0140a0003c0004t0003g0141 | 4 | HG00639.hp2 HG00733.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3320+1842G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56022622 | ||||||
chr4:56022677
|
A | G | 10 | a0001c0001t0006g0031a0001c0001t0006g0043a0001c0001t0006g0044others(7): Show | 10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.3321-1824A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56022677 | ||||||
chr4:56022951
|
G | A | 1 | a0001c0001t0020g0268 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3321-1550G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56022951 | ||||||
chr4:56022992
|
G | A | 1 | a0002c0002t0003g0137 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3321-1509G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56022992 | ||||||
chr4:56023012
|
G | A | 1 | a0002c0002t0006g0150 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3321-1489G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023012 | ||||||
chr4:56023049
|
T | G | 1 | a0001c0001t0012g0160 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3321-1452T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023049 | ||||||
chr4:56023094
|
A | G | 5 | a0002c0002t0003g0042a0002c0002t0003g0130a0002c0002t0003g0135others(2): Show | 7 | HG00738.hp2 HG02055.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.3321-1407A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023094 | ||||||
chr4:56023119
|
G | C | 1 | a0001c0001t0005g0244 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3321-1382G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023119 | ||||||
chr4:56023139
|
G | A | 1 | a0002c0002t0006g0150 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3321-1362G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023139 | ||||||
chr4:56023208
|
C | CA | 4 | a0001c0001t0011g0025a0001c0001t0011g0026a0006c0008t0011g0028others(1): Show | 4 | HG01243.hp2 HG02300.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3321-1291dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr4 | 56023208 | |||||
chr4:56023221
|
C | CA | 59 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0030others(56): Show | 66 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.3321-1269dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr4 | 56023221 | |||||
chr4:56023272
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3321-1229A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023272 | ||||||
chr4:56023470
|
A | C | 3 | a0001c0001t0019g0280a0001c0001t0020g0268a0001c0001t0031g0131 | 3 | HG02109.hp1 HG02258.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3321-1031A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023470 | ||||||
chr4:56023507
|
C | A | 1 | a0001c0001t0002g0099 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3321-994C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023507 | ||||||
chr4:56023572
|
G | A | 1 | a0001c0001t0031g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3321-929G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023572 | ||||||
chr4:56023688
|
AAT | A | 80 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(77): Show | 85 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.3321-803_3321-802d others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr4 | 56023688 | |||||
chr4:56023688
|
AATAT | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0195a0001c0001t0001g0266others(1): Show | 5 | HG00558.hp1 HG00609.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.3321-805_3321-802d others(6): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr4 | 56023688 | |||||
chr4:56023707
|
G | A | 204 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(201): Show | 225 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.3321-794G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023707 | ||||||
chr4:56023752
|
T | C | 1 | a0001c0001t0011g0026 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3321-749T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023752 | ||||||
chr4:56024132
|
ATATAATT others(2): Show |
A | 4 | a0001c0001t0011g0025a0001c0001t0011g0026a0006c0008t0011g0028others(1): Show | 4 | HG01243.hp2 HG02300.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3321-355_3321-347d others(11): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr4 | 56024132 | |||||
chr4:56024368
|
A | G | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.3321-133A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56024368 | ||||||
chr4:56024660
|
A | G | 1 | a0001c0001t0001g0240 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.*11+46A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56024660 | ||||||
chr4:56024764
|
A | G | 9 | a0001c0001t0001g0186a0001c0001t0005g0017a0001c0001t0005g0024others(6): Show | 10 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.*11+150A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56024764 | ||||||
chr4:56024825
|
C | CT | 47 | a0001c0001t0003g0187a0002c0002t0003g0002a0002c0002t0003g0012others(44): Show | 53 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.*11+225dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr4 | 56024825 | |||||
chr4:56025094
|
G | A | 3 | a0001c0001t0007g0004a0001c0001t0007g0027a0001c0001t0007g0053 | 5 | HG02258.hp1 HG02280.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.*11+480G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56025094 | ||||||
chr4:56025101
|
T | C | 126 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(123): Show | 136 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.*11+487T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56025101 | ||||||
chr4:56025727
|
A | C | 1 | a0001c0001t0014g0032 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.*11+1113A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56025727 | ||||||
chr4:56025775
|
A | G | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.*11+1161A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56025775 | ||||||
chr4:56025876
|
T | G | 1 | a0002c0002t0003g0263 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.*11+1262T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56025876 | ||||||
chr4:56025907
|
C | A | 85 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(82): Show | 92 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.*11+1293C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56025907 | ||||||
chr4:56025907
|
C | CA | 45 | a0001c0001t0001g0223a0001c0001t0002g0093a0001c0001t0004g0007others(42): Show | 48 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.*11+1308dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr4 | 56025907 | |||||
chr4:56025946
|
C | A | 3 | a0002c0002t0003g0129a0002c0002t0003g0139a0002c0002t0003g0147 | 3 | HG02129.hp1 NA18952.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.*11+1332C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56025946 | ||||||
chr4:56025999
|
A | G | 10 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(7): Show | 10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.*11+1385A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56025999 | ||||||
chr4:56026163
|
C | T | 2 | a0001c0001t0004g0021a0001c0001t0004g0306 | 3 | HG01975.hp2 HG01981.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.*11+1549C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56026163 | ||||||
chr4:56026165
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.*11+1551C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56026165 | ||||||
chr4:56026183
|
T | A | 48 | a0001c0001t0003g0187a0002c0002t0003g0002a0002c0002t0003g0012others(45): Show | 54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.*11+1569T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56026183 | ||||||
chr4:56026317
|
A | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0219 | 2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.*11+1703A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56026317 | ||||||
chr4:56026529
|
T | C | 1 | a0001c0001t0002g0084 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.*11+1915T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56026529 | ||||||
chr4:56026558
|
C | T | 1 | a0001c0001t0031g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.*11+1944C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56026558 | ||||||
chr4:56026931
|
A | G | 1 | a0002c0002t0003g0152 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.*11+2317A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56026931 | ||||||
chr4:56027003
|
C | T | 47 | a0001c0001t0003g0187a0002c0002t0003g0002a0002c0002t0003g0012others(44): Show | 53 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.*11+2389C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56027003 | ||||||
chr4:56027201
|
T | C | 3 | a0001c0001t0019g0280a0001c0001t0020g0268a0001c0001t0031g0131 | 3 | HG02109.hp1 HG02258.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.*11+2587T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56027201 | ||||||
chr4:56027296
|
A | G | 2 | a0001c0001t0019g0280a0001c0001t0031g0131 | 2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.*11+2682A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56027296 | ||||||
chr4:56027356
|
C | G | 1 | a0001c0001t0005g0220 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.*11+2742C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56027356 | ||||||
chr4:56027520
|
A | G | 2 | a0005c0006t0008g0159a0011c0012t0008g0181 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.*11+2906A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56027520 | ||||||
chr4:56028073
|
C | G | 3 | a0005c0006t0008g0154a0005c0006t0008g0157a0005c0006t0008g0161 | 3 | HG02976.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.*12-3287C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028073 | ||||||
chr4:56028153
|
A | G | 10 | a0001c0001t0006g0031a0001c0001t0006g0043a0001c0001t0006g0044others(7): Show | 10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.*12-3207A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028153 | ||||||
chr4:56028252
|
G | T | 1 | a0004c0005t0001g0242 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.*12-3108G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028252 | ||||||
chr4:56028610
|
GA | G | 7 | a0001c0001t0001g0247a0001c0001t0002g0010a0001c0001t0002g0064others(4): Show | 9 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.*12-2737delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr4 | 56028610 | |||||
chr4:56028630
|
G | T | 1 | a0001c0001t0001g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.*12-2730G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028630 | ||||||
chr4:56028653
|
A | G | 10 | a0001c0001t0012g0155a0001c0001t0012g0156a0001c0001t0012g0158others(7): Show | 10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.*12-2707A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028653 | ||||||
chr4:56028704
|
T | C | 48 | a0001c0001t0003g0187a0002c0002t0003g0002a0002c0002t0003g0012others(45): Show | 54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.*12-2656T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028704 | ||||||
chr4:56028717
|
A | G | 1 | a0001c0001t0019g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.*12-2643A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028717 | ||||||
chr4:56028804
|
A | G | 3 | a0001c0001t0014g0032a0001c0001t0014g0033a0001c0016t0027g0278 | 3 | HG02717.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.*12-2556A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028804 | ||||||
chr4:56028865
|
T | C | 10 | a0001c0001t0006g0031a0001c0001t0006g0043a0001c0001t0006g0044others(7): Show | 10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.*12-2495T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028865 | ||||||
chr4:56028934
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.*12-2426T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028934 | ||||||
chr4:56029014
|
A | G | 2 | a0001c0001t0006g0046a0001c0001t0006g0051 | 2 | HG00280.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.*12-2346A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56029014 | ||||||
chr4:56029077
|
A | G | 3 | a0001c0001t0014g0032a0001c0001t0014g0033a0001c0016t0027g0278 | 3 | HG02717.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.*12-2283A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56029077 | ||||||
chr4:56029160
|
C | A | 4 | a0001c0001t0001g0171a0001c0001t0001g0211a0001c0001t0001g0229others(1): Show | 4 | HG01069.hp2 HG01109.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.*12-2200C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56029160 | ||||||
chr4:56029781
|
G | A | 203 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(200): Show | 224 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.*12-1579G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56029781 | ||||||
chr4:56029842
|
A | C | 8 | a0001c0001t0005g0182a0001c0001t0005g0212a0001c0001t0005g0220others(5): Show | 8 | HG00738.hp1 HG01515.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.*12-1518A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56029842 | ||||||
chr4:56029875
|
T | A | 2 | a0001c0001t0004g0021a0001c0001t0004g0306 | 3 | HG01975.hp2 HG01981.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.*12-1485T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56029875 | ||||||
chr4:56030253
|
A | G | 1 | a0001c0001t0004g0289 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.*12-1107A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56030253 | ||||||
chr4:56030413
|
G | A | 1 | a0001c0001t0006g0050 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.*12-947G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56030413 | ||||||
chr4:56030477
|
C | T | 2 | a0001c0001t0002g0077a0001c0001t0004g0295 | 2 | HG03471.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.*12-883C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56030477 | ||||||
chr4:56030782
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.*12-578C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56030782 | ||||||
chr4:56030961
|
C | T | 1 | a0001c0001t0020g0268 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.*12-399C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56030961 | ||||||
chr4:56031039
|
GAAGGATC others(18): Show |
G | 6 | a0001c0003t0003g0003a0001c0003t0003g0019a0001c0003t0003g0273others(3): Show | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.*12-317_*12-293del others(25): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr4 | 56031039 | |||||
chr4:56031088
|
C | T | 79 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(76): Show | 84 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.*12-272C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56031088 |