geneid | 64793 |
---|---|
ensemblid | ENSG00000130695.16 |
hgncid | 25309 |
symbol | CEP85 |
name | centrosomal protein 85 |
refseq_nuc | NM_001319944.2 |
refseq_prot | NP_001306873.1 |
ensembl_nuc | ENST00000451429.8 |
ensembl_prot | ENSP00000417002.3 |
mane_status | MANE Select |
chr | chr1 |
start | 26234200 |
end | 26278808 |
strand | + |
ver | v1.2 |
region | chr1:26234200-26278808 |
region5000 | chr1:26229200-26283808 |
regionname0 | CEP85_chr1_26234200_26278808 |
regionname5000 | CEP85_chr1_26229200_26283808 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 761 | 226 | 56 | 42 | 95 | 6 | 25 | 78 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0002 | 0/0 | 761 | 73 | 4 | 17 | 43 | 4 | 5 | 31 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0003 | 0/0 | 761 | 28 | 12 | 4 | 1 | 6 | 5 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0004 | 0/0 | 761 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0005 | 0/0 | 761 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0006 | 0/0 | 761 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0007 | 0/0 | 761 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0008 | 0/0 | 761 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0009 | 0/0 | 761 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0010 | 0/0 | 761 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2286 | 223 | 55 | 40 | 95 | 6 | 25 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
c0002 | 0/0 | 2286 | 72 | 4 | 16 | 43 | 4 | 5 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
c0003 | 0/0 | 2286 | 21 | 7 | 4 | 1 | 6 | 3 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
c0004 | 0/0 | 2286 | 5 | 5 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
c0005 | 0/0 | 2286 | 3 | 3 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
c0006 | 0/0 | 2286 | 3 | 3 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
c0007 | 0/0 | 2286 | 2 | 2 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
c0008 | 0/0 | 2286 | 2 | 0 | 0 | 0 | 0 | 2 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
c0009 | 0/0 | 2286 | 2 | 0 | 2 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
c0010 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
c0011 | 0/0 | 2286 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
c0012 | 0/0 | 2286 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
c0013 | 0/0 | 2286 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
c0014 | 0/0 | 2286 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
c0015 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
c0016 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
c0017 | 0/0 | 2286 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
c0018 | 0/0 | 2286 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1649 | 119 | 27 | 29 | 43 | 9 | 11 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
t0002 | 1/0 | 1649 | 85 | 10 | 4 | 60 | 0 | 10 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
t0003 | 0/1 | 1649 | 79 | 29 | 13 | 27 | 1 | 8 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
t0004 | 0/0 | 1651 | 25 | 12 | 2 | 1 | 4 | 6 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
t0005 | 0/0 | 1649 | 19 | 0 | 15 | 4 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
t0006 | 0/0 | 1651 | 4 | 0 | 2 | 0 | 2 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
t0007 | 0/0 | 1649 | 4 | 0 | 0 | 4 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
t0008 | 0/0 | 1649 | 3 | 2 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
t0009 | 0/0 | 1649 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
t0010 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
t0011 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
t0012 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 2 | 4 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0003 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0007 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2286 | 223 | 55 | 40 | 95 | 6 | 25 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0001c0009 | 0/0 | 2286 | 2 | 0 | 2 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0001c0016 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0002c0002 | 0/0 | 2286 | 72 | 4 | 16 | 43 | 4 | 5 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0002c0012 | 0/0 | 2286 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0003c0003 | 0/0 | 2286 | 21 | 7 | 4 | 1 | 6 | 3 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0003c0005 | 0/0 | 2286 | 3 | 3 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0003c0007 | 0/0 | 2286 | 2 | 2 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0003c0008 | 0/0 | 2286 | 2 | 0 | 0 | 0 | 0 | 2 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0004c0004 | 0/0 | 2286 | 5 | 5 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0004c0010 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0004c0011 | 0/0 | 2286 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0005c0006 | 0/0 | 2286 | 3 | 3 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0006c0018 | 0/0 | 2286 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0007c0013 | 0/0 | 2286 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0008c0015 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0009c0014 | 0/0 | 2286 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0010c0017 | 0/0 | 2286 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3934 | 48 | 20 | 12 | 5 | 5 | 6 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0001c0001t0002 | 1/0 | 3934 | 84 | 10 | 4 | 59 | 0 | 10 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0001c0001t0003 | 0/1 | 3934 | 71 | 24 | 10 | 27 | 1 | 8 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0001c0001t0005 | 0/0 | 3934 | 18 | 0 | 14 | 4 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0001c0001t0009 | 0/0 | 3934 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0001c0001t0012 | 0/0 | 3934 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0001c0009t0003 | 0/0 | 3934 | 2 | 0 | 2 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0001c0016t0011 | 0/0 | 3934 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0002c0002t0001 | 0/0 | 3934 | 67 | 4 | 16 | 38 | 4 | 5 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0002c0002t0007 | 0/0 | 3934 | 4 | 0 | 0 | 4 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0002c0002t0010 | 0/0 | 3934 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0002c0012t0001 | 0/0 | 3934 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0003c0003t0004 | 0/0 | 3936 | 17 | 7 | 2 | 1 | 4 | 3 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0003c0003t0006 | 0/0 | 3936 | 4 | 0 | 2 | 0 | 2 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0003c0005t0004 | 0/0 | 3936 | 3 | 3 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0003c0007t0004 | 0/0 | 3936 | 2 | 2 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0003c0008t0004 | 0/0 | 3936 | 2 | 0 | 0 | 0 | 0 | 2 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0004c0004t0003 | 0/0 | 3934 | 3 | 3 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0004c0004t0008 | 0/0 | 3934 | 2 | 2 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0004c0010t0003 | 0/0 | 3934 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0004c0011t0008 | 0/0 | 3934 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0005c0006t0001 | 0/0 | 3934 | 3 | 3 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0006c0018t0003 | 0/0 | 3934 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0007c0013t0005 | 0/0 | 3934 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0008c0015t0003 | 0/0 | 3934 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0009c0014t0002 | 0/0 | 3934 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
a0010c0017t0004 | 0/0 | 3936 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | copy fasta | chr1 | 26229200 | 26283808 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0007 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0003 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0005g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0005g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0005g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0005g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0005g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0005g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0005g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0009g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0001t0012g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0009t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0009t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0001c0016t0011g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0007g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0007g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0007g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0007g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0002t0010g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0002c0012t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0004g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0004g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0004g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0004g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0004g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0004g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0004g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0004g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0004g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0004g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0006g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0006g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0006g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0003t0006g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0005t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0005t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0005t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0007t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0007t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0008t0004g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0003c0008t0004g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0004c0004t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0004c0004t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0004c0004t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0004c0004t0008g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0004c0004t0008g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0004c0010t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0004c0011t0008g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0005c0006t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0005c0006t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0005c0006t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0006c0018t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0007c0013t0005g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0008c0015t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0009c0014t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
a0010c0017t0004g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0233 | EUR | GBR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | GBR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | GBR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00140 | hp2 | a0003 | c0003 | t0004 | g0311 | EUR | GBR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0226 | EUR | FIN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00280 | hp2 | a0003 | c0003 | t0006 | g0094 | EUR | FIN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00323 | hp1 | a0003 | c0003 | t0004 | g0302 | EUR | FIN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0107 | EUR | FIN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00558 | hp1 | a0009 | c0014 | t0002 | g0063 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00621 | hp2 | a0002 | c0002 | t0010 | g0283 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00639 | hp1 | a0004 | c0011 | t0008 | g0291 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0100 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0019 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00733 | hp1 | a0003 | c0003 | t0006 | g0095 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00741 | hp1 | a0003 | c0003 | t0004 | g0312 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0241 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01069 | hp2 | a0001 | c0009 | t0003 | g0108 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01071 | hp2 | a0001 | c0009 | t0003 | g0111 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0274 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01081 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01099 | hp1 | a0001 | c0001 | t0005 | g0018 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01106 | hp1 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0121 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01192 | hp2 | a0006 | c0018 | t0003 | g0123 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0221 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0227 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0254 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01361 | hp1 | a0003 | c0003 | t0006 | g0096 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0240 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0215 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0027 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01496 | hp2 | a0001 | c0001 | t0005 | g0023 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01515 | hp1 | a0003 | c0003 | t0006 | g0093 | EUR | IBS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | IBS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0217 | EUR | IBS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01516 | hp2 | a0003 | c0003 | t0004 | g0317 | EUR | IBS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01517 | hp1 | a0003 | c0003 | t0004 | g0310 | EUR | IBS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | IBS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01934 | hp1 | a0007 | c0013 | t0005 | g0028 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0015 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0126 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01952 | hp2 | a0001 | c0001 | t0005 | g0024 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0242 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01975 | hp2 | a0001 | c0001 | t0005 | g0026 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0263 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01993 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0235 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0016 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02004 | hp2 | a0003 | c0003 | t0004 | g0305 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02056 | hp1 | a0002 | c0002 | t0007 | g0280 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02080 | hp2 | a0001 | c0001 | t0005 | g0022 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0276 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0265 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02148 | hp2 | a0001 | c0001 | t0005 | g0084 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0247 | EAS | CDX | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02257 | hp2 | a0004 | c0004 | t0003 | g0292 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0273 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0275 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0239 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0132 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02300 | hp2 | a0001 | c0001 | t0005 | g0083 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02572 | hp1 | a0003 | c0003 | t0004 | g0318 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0143 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02615 | hp1 | a0004 | c0004 | t0003 | g0296 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0218 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02622 | hp2 | a0003 | c0005 | t0004 | g0322 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02630 | hp2 | a0005 | c0006 | t0001 | g0261 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02647 | hp1 | a0003 | c0007 | t0004 | g0320 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02647 | hp2 | a0005 | c0006 | t0001 | g0278 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02683 | hp2 | a0003 | c0003 | t0004 | g0319 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02723 | hp1 | a0004 | c0010 | t0003 | g0290 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02809 | hp1 | a0001 | c0016 | t0011 | g0324 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02895 | hp2 | a0005 | c0006 | t0001 | g0260 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02896 | hp1 | a0003 | c0003 | t0004 | g0301 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02896 | hp2 | a0003 | c0005 | t0004 | g0323 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02897 | hp2 | a0003 | c0003 | t0004 | g0300 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0271 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02976 | hp2 | a0008 | c0015 | t0003 | g0163 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03017 | hp1 | a0001 | c0001 | t0009 | g0001 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03041 | hp1 | a0003 | c0003 | t0004 | g0303 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | MSL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | MSL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03195 | hp1 | a0003 | c0005 | t0004 | g0297 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0137 | AFR | MSL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0145 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | MSL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03486 | hp2 | a0003 | c0003 | t0004 | g0316 | AFR | MSL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03491 | hp1 | a0003 | c0008 | t0004 | g0309 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03492 | hp2 | a0003 | c0008 | t0004 | g0308 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03516 | hp1 | a0004 | c0004 | t0008 | g0294 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | MSL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0232 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03710 | hp2 | a0003 | c0003 | t0004 | g0304 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | BEB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0105 | SAS | BEB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0281 | SAS | BEB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0122 | SAS | BEB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | BEB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0151 | SAS | BEB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | BEB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG04115 | hp1 | a0010 | c0017 | t0004 | g0306 | SAS | STU | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | STU | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG04199 | hp1 | a0003 | c0003 | t0004 | g0314 | SAS | STU | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0152 | SAS | STU | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | STU | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | STU | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0246 | SAS | STU | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | YRI | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18522 | hp2 | a0003 | c0003 | t0004 | g0325 | AFR | YRI | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | CHB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18612 | hp2 | a0002 | c0002 | t0007 | g0004 | EAS | CHB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | YRI | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18906 | hp2 | a0004 | c0004 | t0008 | g0293 | AFR | YRI | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18960 | hp2 | a0002 | c0002 | t0007 | g0238 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18962 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18980 | hp2 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA18997 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | LWK | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19030 | hp2 | a0003 | c0003 | t0004 | g0313 | AFR | LWK | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19043 | hp1 | a0004 | c0004 | t0003 | g0295 | AFR | LWK | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | LWK | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19067 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19080 | hp1 | a0003 | c0003 | t0004 | g0307 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19083 | hp2 | a0002 | c0002 | t0007 | g0213 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | YRI | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | YRI | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ASW | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ASW | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0212 | EUR | TSI | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | TSI | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG01123 | hp2 | a0002 | c0012 | t0001 | g0187 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02486 | hp1 | a0001 | c0001 | t0012 | g0168 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG02486 | hp2 | a0003 | c0007 | t0004 | g0321 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | USA | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | USA | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | LWK | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0141 | REF | REF | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0007 | REF | REF | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:26244166
|
G | T | 1 | a0006 | 1 | HG01192.hp2 | missense_variant&splice_region_variant | MODERATE | c.56G>T | p.Ser19Ile | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/14 | 189/3934 | 56/2286 | 19/761 | chr1 | 26244166 | ||
chr1:26244205
|
A | G | 1 | a0010 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.95A>G | p.Glu32Gly | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/14 | 228/3934 | 95/2286 | 32/761 | chr1 | 26244205 | ||
chr1:26244253
|
G | A | 1 | a0004 | 7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
missense_variant | MODERATE | c.143G>A | p.Arg48His | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/14 | 276/3934 | 143/2286 | 48/761 | chr1 | 26244253 | ||
chr1:26255600
|
G | A | 1 | a0002 | 73 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(70): Show |
missense_variant | MODERATE | c.638G>A | p.Ser213Asn | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/14 | 771/3934 | 638/2286 | 213/761 | chr1 | 26255600 | ||
chr1:26255849
|
A | G | 1 | a0005 | 3 | HG02630.hp2 HG02647.hp2 HG02895.hp2 |
missense_variant | MODERATE | c.887A>G | p.Gln296Arg | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/14 | 1020/3934 | 887/2286 | 296/761 | chr1 | 26255849 | ||
chr1:26258178
|
T | C | 1 | a0007 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.1073T>C | p.Val358Ala | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/14 | 1206/3934 | 1073/2286 | 358/761 | chr1 | 26258178 | ||
chr1:26259676
|
G | T | 1 | a0008 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.1215G>T | p.Leu405Phe | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/14 | 1348/3934 | 1215/2286 | 405/761 | chr1 | 26259676 | ||
chr1:26269589
|
G | A | 2 | a0003a0010 | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
missense_variant | MODERATE | c.1624G>A | p.Ala542Thr | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/14 | 1757/3934 | 1624/2286 | 542/761 | chr1 | 26269589 | ||
chr1:26269604
|
G | A | 1 | a0009 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.1639G>A | p.Ala547Thr | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/14 | 1772/3934 | 1639/2286 | 547/761 | chr1 | 26269604 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:26244269
|
C | A | 1 | a0004c0010 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.159C>A | p.Ala53Ala | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/14 | 292/3934 | 159/2286 | 53/761 | chr1 | 26244269 | ||
chr1:26255490
|
G | A | 2 | a0003c0005a0003c0007 | 5 | HG02486.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
synonymous_variant | LOW | c.528G>A | p.Ala176Ala | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/14 | 661/3934 | 528/2286 | 176/761 | chr1 | 26255490 | ||
chr1:26255769
|
G | A | 1 | a0003c0008 | 2 | HG03491.hp1 HG03492.hp2 |
synonymous_variant | LOW | c.807G>A | p.Pro269Pro | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/14 | 940/3934 | 807/2286 | 269/761 | chr1 | 26255769 | ||
chr1:26257653
|
C | A | 1 | a0003c0007 | 2 | HG02486.hp2 HG02647.hp1 |
synonymous_variant | LOW | c.960C>A | p.Ile320Ile | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 5/14 | 1093/3934 | 960/2286 | 320/761 | chr1 | 26257653 | ||
chr1:26257680
|
C | T | 1 | a0001c0009 | 2 | HG01069.hp2 HG01071.hp2 |
synonymous_variant | LOW | c.987C>T | p.Ile329Ile | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 5/14 | 1120/3934 | 987/2286 | 329/761 | chr1 | 26257680 | ||
chr1:26259619
|
A | G | 1 | a0001c0016 | 1 | HG02809.hp1 | splice_region_variant&synonymous_variant | LOW | c.1158A>G | p.Glu386Glu | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/14 | 1291/3934 | 1158/2286 | 386/761 | chr1 | 26259619 | ||
chr1:26259652
|
G | A | 1 | a0002c0012 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.1191G>A | p.Gln397Gln | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/14 | 1324/3934 | 1191/2286 | 397/761 | chr1 | 26259652 | ||
chr1:26271047
|
T | C | 1 | a0004c0011 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.1683T>C | p.Ser561Ser | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/14 | 1816/3934 | 1683/2286 | 561/761 | chr1 | 26271047 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:26234243
|
A | G | 1 | a0001c0001t0012 | 1 | HG02486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-90A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/14 | 5541 | chr1 | 26234243 | |||||
chr1:26234254
|
G | A | 10 | a0001c0001t0003a0001c0001t0012a0001c0009t0003others(7): Show | 87 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(84): Show |
5_prime_UTR_variant | MODIFIER | c.-79G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/14 | 5530 | chr1 | 26234254 | |||||
chr1:26277392
|
G | GAA | 6 | a0003c0003t0004a0003c0003t0006a0003c0005t0004others(3): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*99_*100insAA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 100 | chr1 | 26277392 | |||||
chr1:26277502
|
A | C | 22 | a0001c0001t0001a0001c0001t0003a0001c0001t0012others(19): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*209A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 209 | chr1 | 26277502 | |||||
chr1:26277580
|
T | G | 6 | a0003c0003t0004a0003c0003t0006a0003c0005t0004others(3): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*287T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 287 | chr1 | 26277580 | |||||
chr1:26277865
|
G | A | 1 | a0002c0002t0010 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*572G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 572 | chr1 | 26277865 | |||||
chr1:26277880
|
G | A | 1 | a0001c0001t0009 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*587G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 587 | chr1 | 26277880 | |||||
chr1:26277900
|
C | A | 2 | a0004c0004t0008a0004c0011t0008 | 3 | HG00639.hp1 HG03516.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*607C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 607 | chr1 | 26277900 | |||||
chr1:26278031
|
C | A | 2 | a0001c0001t0005a0007c0013t0005 | 19 | HG00642.hp2 HG00738.hp2 HG01081.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*738C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 738 | chr1 | 26278031 | |||||
chr1:26278450
|
G | A | 1 | a0002c0002t0007 | 4 | HG02056.hp1 NA18612.hp2 NA18960.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1157G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 1157 | chr1 | 26278450 | |||||
chr1:26278578
|
T | C | 6 | a0003c0003t0004a0003c0003t0006a0003c0005t0004others(3): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1285T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 1285 | chr1 | 26278578 | |||||
chr1:26278650
|
C | T | 1 | a0001c0016t0011 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1357C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 1357 | chr1 | 26278650 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:26234454
|
C | G | 239 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(236): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.-23+144C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26234454 | ||||||
chr1:26234471
|
C | T | 26 | a0001c0001t0001g0315a0001c0016t0011g0324a0003c0003t0004g0300others(23): Show | 26 | HG00140.hp2 HG00323.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.-23+161C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26234471 | ||||||
chr1:26234596
|
C | T | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG01167.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-23+286C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26234596 | ||||||
chr1:26234705
|
A | G | 1 | a0003c0003t0004g0325 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-23+395A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26234705 | ||||||
chr1:26234729
|
G | C | 78 | a0001c0001t0003g0003a0001c0001t0003g0092a0001c0001t0003g0097others(75): Show | 80 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-23+419G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26234729 | ||||||
chr1:26234749
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-23+439G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26234749 | ||||||
chr1:26234952
|
G | A | 1 | a0001c0001t0003g0092 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-23+642G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26234952 | ||||||
chr1:26234970
|
A | G | 1 | a0003c0005t0004g0297 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-23+660A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26234970 | ||||||
chr1:26235268
|
C | T | 7 | a0004c0004t0003g0292a0004c0004t0003g0295a0004c0004t0003g0296others(4): Show | 7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23+958C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26235268 | ||||||
chr1:26235310
|
A | G | 3 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289 | 3 | HG01081.hp1 HG01346.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-23+1000A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26235310 | ||||||
chr1:26235326
|
T | C | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012 | 3 | HG00597.hp1 NA18960.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-23+1016T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26235326 | ||||||
chr1:26235365
|
T | C | 29 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.-23+1055T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26235365 | ||||||
chr1:26235393
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-23+1083G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26235393 | ||||||
chr1:26235540
|
A | G | 232 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.-23+1230A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26235540 | ||||||
chr1:26235564
|
A | ATTTTTTT others(3): Show |
1 | a0003c0005t0004g0323 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-23+1256_-23+1257i others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235564 | |||||
chr1:26235567
|
C | CT | 45 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(42): Show | 45 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-23+1277dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | |||||
chr1:26235567
|
C | CTT | 139 | a0001c0001t0001g0214a0001c0001t0001g0248a0001c0001t0001g0266others(136): Show | 144 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.-23+1276_-23+1277d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | |||||
chr1:26235567
|
C | CTTT | 12 | a0001c0001t0003g0161a0001c0001t0003g0162a0001c0001t0003g0164others(9): Show | 12 | HG00621.hp2 HG02056.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-23+1275_-23+1277d others(5): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | |||||
chr1:26235567
|
C | CTTTTTTT others(3): Show |
10 | a0003c0003t0004g0301a0003c0003t0004g0302a0003c0003t0004g0303others(7): Show | 10 | HG00323.hp1 HG01515.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.-23+1268_-23+1277d others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | |||||
chr1:26235567
|
C | CTTTTTTT others(4): Show |
9 | a0001c0001t0001g0315a0003c0003t0004g0310a0003c0003t0004g0311others(6): Show | 9 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.-23+1267_-23+1277d others(13): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | |||||
chr1:26235567
|
C | CTTTTTTT others(5): Show |
2 | a0003c0003t0004g0317a0003c0003t0006g0096 | 2 | HG01361.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-23+1266_-23+1277d others(14): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | |||||
chr1:26235567
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0012g0168a0003c0003t0004g0318a0003c0003t0004g0319 | 3 | HG02486.hp1 HG02572.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-23+1265_-23+1277d others(15): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | |||||
chr1:26235567
|
C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0284a0004c0011t0008g0291 | 2 | HG00639.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-23+1261_-23+1277d others(19): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | |||||
chr1:26235567
|
C | CTTTTTTT others(11): Show |
5 | a0001c0001t0001g0285a0004c0004t0003g0292a0004c0004t0003g0295others(2): Show | 5 | HG01891.hp2 HG02257.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+1260_-23+1277d others(20): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | |||||
chr1:26235567
|
C | CTTTTTTT others(14): Show |
1 | a0004c0004t0003g0296 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-23+1277_-23+1278i others(23): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | |||||
chr1:26235567
|
C | T | 5 | a0002c0002t0001g0286a0003c0005t0004g0322a0003c0005t0004g0323others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+1257C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26235567 | ||||||
chr1:26235813
|
C | A | 119 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(116): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-23+1503C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26235813 | ||||||
chr1:26236023
|
G | A | 1 | a0001c0001t0002g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-23+1713G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26236023 | ||||||
chr1:26236152
|
C | T | 2 | a0003c0008t0004g0308a0003c0008t0004g0309 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-23+1842C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26236152 | ||||||
chr1:26236240
|
G | T | 1 | a0001c0001t0005g0083 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-23+1930G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26236240 | ||||||
chr1:26236270
|
T | C | 324 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(321): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.-23+1960T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26236270 | ||||||
chr1:26236394
|
C | CT | 21 | a0001c0001t0001g0211a0001c0001t0001g0284a0001c0001t0001g0285others(18): Show | 21 | HG00639.hp1 HG01099.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-23+2097dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26236394 | |||||
chr1:26236407
|
T | C | 17 | a0001c0001t0005g0002a0001c0001t0005g0015a0001c0001t0005g0016others(14): Show | 19 | HG00642.hp2 HG00738.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+2097T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26236407 | ||||||
chr1:26236408
|
C | T | 227 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(224): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.-23+2098C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26236408 | ||||||
chr1:26236614
|
G | A | 119 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(116): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-23+2304G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26236614 | ||||||
chr1:26236923
|
G | A | 1 | a0001c0001t0003g0098 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-23+2613G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26236923 | ||||||
chr1:26237174
|
G | A | 3 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289 | 3 | HG01081.hp1 HG01346.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-22-2588G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237174 | ||||||
chr1:26237205
|
T | G | 1 | a0002c0002t0001g0286 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-22-2557T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237205 | ||||||
chr1:26237252
|
C | A | 1 | a0001c0001t0001g0214 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-22-2510C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237252 | ||||||
chr1:26237359
|
T | G | 84 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0003g0003others(81): Show | 86 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.-22-2403T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237359 | ||||||
chr1:26237416
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-22-2346A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237416 | ||||||
chr1:26237441
|
A | G | 1 | a0001c0001t0002g0080 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-22-2321A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237441 | ||||||
chr1:26237621
|
T | C | 3 | a0001c0001t0003g0099a0001c0001t0003g0100a0001c0001t0003g0101 | 3 | HG00639.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-22-2141T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237621 | ||||||
chr1:26237739
|
C | A | 29 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.-22-2023C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237739 | ||||||
chr1:26237755
|
T | C | 1 | a0001c0001t0005g0015 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-22-2007T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237755 | ||||||
chr1:26237805
|
C | T | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG01167.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-22-1957C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237805 | ||||||
chr1:26238067
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-22-1695T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26238067 | ||||||
chr1:26238202
|
C | CTTTTTT | 28 | a0001c0001t0001g0178a0001c0001t0001g0299a0001c0001t0003g0103others(25): Show | 28 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.-22-1549_-22-1544d others(8): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26238202 | |||||
chr1:26238202
|
C | CTTTTTTT | 167 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0179others(164): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.-22-1550_-22-1544d others(9): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26238202 | |||||
chr1:26238202
|
C | CTTTTTTT others(1): Show |
33 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(30): Show | 33 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.-22-1551_-22-1544d others(10): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26238202 | |||||
chr1:26238344
|
G | A | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-22-1418G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26238344 | ||||||
chr1:26238347
|
C | T | 29 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.-22-1415C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26238347 | ||||||
chr1:26238389
|
C | T | 2 | a0001c0001t0003g0100a0001c0001t0003g0101 | 2 | HG00639.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-22-1373C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26238389 | ||||||
chr1:26238415
|
C | T | 6 | a0001c0001t0003g0099a0001c0001t0003g0100a0001c0001t0003g0101others(3): Show | 6 | HG00639.hp2 HG01099.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22-1347C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26238415 | ||||||
chr1:26238447
|
C | T | 1 | a0001c0016t0011g0324 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-22-1315C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26238447 | ||||||
chr1:26238478
|
G | A | 1 | a0001c0001t0003g0104 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-22-1284G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26238478 | ||||||
chr1:26238492
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-22-1270G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26238492 | ||||||
chr1:26239174
|
G | A | 232 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.-22-588G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26239174 | ||||||
chr1:26239355
|
T | A | 10 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0016t0011g0324others(7): Show | 10 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-22-407T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26239355 | ||||||
chr1:26239534
|
T | C | 1 | a0002c0002t0001g0215 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-22-228T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26239534 | ||||||
chr1:26239551
|
CATGTTGG others(56): Show |
C | 9 | a0001c0001t0001g0284a0001c0001t0001g0285a0004c0004t0003g0292others(6): Show | 9 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-22-210_-22-148del others(63): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26239551 | ||||||
chr1:26239599
|
G | A | 1 | a0001c0001t0002g0029 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-22-163G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26239599 | ||||||
chr1:26239696
|
G | A | 6 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(3): Show | 6 | HG00140.hp1 HG01496.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-66G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26239696 | ||||||
chr1:26240126
|
A | G | 1 | a0002c0002t0001g0272 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.55+288A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240126 | ||||||
chr1:26240194
|
A | G | 232 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.55+356A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240194 | ||||||
chr1:26240275
|
C | T | 2 | a0002c0002t0001g0271a0002c0002t0001g0276 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.55+437C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240275 | ||||||
chr1:26240378
|
C | T | 3 | a0001c0001t0002g0077a0001c0001t0002g0078a0001c0001t0002g0079 | 3 | HG02129.hp2 NA18954.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.55+540C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240378 | ||||||
chr1:26240422
|
G | A | 1 | a0001c0001t0003g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.55+584G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240422 | ||||||
chr1:26240553
|
A | G | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.55+715A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240553 | ||||||
chr1:26240751
|
C | T | 118 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(115): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.55+913C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240751 | ||||||
chr1:26240774
|
A | T | 1 | a0004c0004t0003g0295 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.55+936A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240774 | ||||||
chr1:26240869
|
G | A | 1 | a0001c0001t0005g0016 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.55+1031G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240869 | ||||||
chr1:26240894
|
T | C | 1 | a0002c0002t0001g0216 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.55+1056T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240894 | ||||||
chr1:26240913
|
A | G | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG01167.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.55+1075A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240913 | ||||||
chr1:26241163
|
A | G | 1 | a0003c0003t0004g0314 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.55+1325A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241163 | ||||||
chr1:26241243
|
A | ATTTTTTT others(5): Show |
24 | a0001c0001t0001g0315a0003c0003t0004g0302a0003c0003t0004g0303others(21): Show | 24 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.55+1405_55+1406ins others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241243 | ||||||
chr1:26241243
|
A | ATTTTTTT others(6): Show |
6 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0003t0004g0313others(3): Show | 6 | HG01361.hp1 HG01515.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+1405_55+1406ins others(13): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241243 | ||||||
chr1:26241244
|
A | ATTTTTTT others(2): Show |
6 | a0001c0001t0003g0106a0001c0001t0003g0107a0002c0002t0001g0217others(3): Show | 6 | HG00323.hp2 HG01516.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.55+1414_55+1422dup others(9): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26241244 | |||||
chr1:26241244
|
A | ATTTTTTT others(3): Show |
149 | a0001c0001t0001g0169a0001c0001t0001g0179a0001c0001t0001g0186others(146): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.55+1413_55+1422dup others(10): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26241244 | |||||
chr1:26241244
|
A | ATTTTTTT others(4): Show |
40 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0001t0001g0181others(37): Show | 40 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.55+1412_55+1422dup others(11): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26241244 | |||||
chr1:26241244
|
A | ATTTTTTT others(5): Show |
6 | a0001c0001t0001g0177a0001c0001t0001g0269a0001c0001t0001g0284others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.55+1411_55+1422dup others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26241244 | |||||
chr1:26241244
|
A | T | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.55+1406A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241244 | ||||||
chr1:26241318
|
C | T | 1 | a0001c0001t0003g0157 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.55+1480C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241318 | ||||||
chr1:26241389
|
C | G | 118 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(115): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.55+1551C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241389 | ||||||
chr1:26241392
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.55+1554G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241392 | ||||||
chr1:26241411
|
T | A | 2 | a0003c0003t0004g0310a0003c0003t0004g0317 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.55+1573T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241411 | ||||||
chr1:26241446
|
A | G | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.55+1608A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241446 | ||||||
chr1:26241502
|
G | A | 5 | a0001c0001t0003g0106a0001c0001t0003g0109a0001c0001t0003g0110others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+1664G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241502 | ||||||
chr1:26241674
|
A | G | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.55+1836A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241674 | ||||||
chr1:26241839
|
G | C | 1 | a0002c0002t0001g0221 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.55+2001G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241839 | ||||||
chr1:26241971
|
A | C | 1 | a0001c0001t0002g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.55+2133A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241971 | ||||||
chr1:26242032
|
G | A | 1 | a0002c0002t0001g0273 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.56-2134G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242032 | ||||||
chr1:26242051
|
T | C | 118 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(115): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.56-2115T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242051 | ||||||
chr1:26242207
|
A | G | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.56-1959A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242207 | ||||||
chr1:26242224
|
G | A | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.56-1942G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242224 | ||||||
chr1:26242421
|
G | A | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.56-1745G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242421 | ||||||
chr1:26242435
|
G | A | 23 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(20): Show | 23 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.56-1731G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242435 | ||||||
chr1:26242539
|
G | A | 1 | a0001c0001t0002g0031 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.56-1627G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242539 | ||||||
chr1:26242637
|
G | A | 1 | a0001c0001t0003g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.56-1529G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242637 | ||||||
chr1:26242794
|
T | TTTTG | 223 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(220): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.56-1360_56-1357dup others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26242794 | |||||
chr1:26242976
|
T | C | 5 | a0001c0001t0001g0179a0001c0001t0001g0186a0001c0001t0001g0195others(2): Show | 5 | HG01255.hp1 HG02280.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-1190T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242976 | ||||||
chr1:26242988
|
C | T | 7 | a0004c0004t0003g0292a0004c0004t0003g0295a0004c0004t0003g0296others(4): Show | 7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.56-1178C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242988 | ||||||
chr1:26243020
|
G | T | 7 | a0004c0004t0003g0292a0004c0004t0003g0295a0004c0004t0003g0296others(4): Show | 7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.56-1146G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243020 | ||||||
chr1:26243025
|
C | A | 2 | a0003c0008t0004g0308a0003c0008t0004g0309 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.56-1141C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243025 | ||||||
chr1:26243120
|
G | A | 239 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(236): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.56-1046G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243120 | ||||||
chr1:26243128
|
CTT | C | 224 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(221): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.56-1020_56-1019del others(2): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26243128 | |||||
chr1:26243131
|
T | C | 2 | a0003c0007t0004g0320a0003c0007t0004g0321 | 2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.56-1035T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243131 | ||||||
chr1:26243132
|
T | C | 1 | a0001c0001t0002g0170 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.56-1034T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243132 | ||||||
chr1:26243194
|
G | A | 10 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0016t0011g0324others(7): Show | 10 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.56-972G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243194 | ||||||
chr1:26243208
|
C | A | 1 | a0001c0001t0003g0161 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.56-958C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243208 | ||||||
chr1:26243293
|
G | A | 1 | a0002c0002t0001g0222 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.56-873G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243293 | ||||||
chr1:26243311
|
GTCTTGGT others(3): Show |
G | 72 | a0001c0001t0003g0003a0001c0001t0003g0092a0001c0001t0003g0098others(69): Show | 74 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.56-854_56-845delTC others(8): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243311 | ||||||
chr1:26243312
|
T | G | 160 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(157): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.56-854T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243312 | ||||||
chr1:26243330
|
G | A | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.56-836G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243330 | ||||||
chr1:26243476
|
A | G | 11 | a0001c0001t0005g0002a0001c0001t0005g0015a0001c0001t0005g0016others(8): Show | 13 | HG00738.hp2 HG01081.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.56-690A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243476 | ||||||
chr1:26243499
|
C | A | 118 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(115): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.56-667C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243499 | ||||||
chr1:26243518
|
G | A | 23 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(20): Show | 23 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.56-648G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243518 | ||||||
chr1:26243770
|
C | T | 8 | a0001c0001t0003g0098a0001c0001t0003g0136a0001c0001t0003g0137others(5): Show | 8 | HG02258.hp2 HG02622.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.56-396C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243770 | ||||||
chr1:26243825
|
G | C | 232 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.56-341G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243825 | ||||||
chr1:26243927
|
G | A | 3 | a0001c0001t0003g0146a0001c0001t0003g0147a0001c0001t0003g0159 | 3 | HG01099.hp2 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.56-239G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243927 | ||||||
chr1:26243969
|
G | T | 1 | a0002c0002t0001g0262 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.56-197G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243969 | ||||||
chr1:26243991
|
C | CA | 41 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0002g0031others(38): Show | 41 | HG00639.hp2 HG01099.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.56-149dupA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26243991 | |||||
chr1:26243991
|
C | CAA | 27 | a0001c0001t0001g0315a0001c0001t0003g0109a0001c0001t0003g0110others(24): Show | 27 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.56-150_56-149dupAA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26243991 | |||||
chr1:26243991
|
C | CAAA | 9 | a0001c0009t0003g0108a0003c0003t0004g0300a0003c0003t0004g0301others(6): Show | 9 | HG00323.hp1 HG01069.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.56-151_56-149dupAA others(1): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26243991 | |||||
chr1:26243991
|
C | CAAAA | 9 | a0001c0001t0001g0284a0001c0001t0003g0106a0004c0004t0003g0292others(6): Show | 9 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.56-152_56-149dupAA others(2): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26243991 | |||||
chr1:26243991
|
CA | C | 9 | a0001c0001t0002g0070a0001c0001t0002g0071a0001c0001t0002g0072others(6): Show | 9 | HG00544.hp2 HG02040.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.56-149delA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26243991 | |||||
chr1:26243991
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0214a0002c0002t0001g0216 | 2 | NA18961.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.56-158_56-149delAA others(8): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26243991 | |||||
chr1:26243991
|
CAAAAAAA others(4): Show |
C | 115 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(112): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.56-159_56-149delAA others(9): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26243991 | |||||
chr1:26244465
|
C | G | 11 | a0001c0001t0005g0002a0001c0001t0005g0015a0001c0001t0005g0016others(8): Show | 13 | HG00738.hp2 HG01081.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.208+147C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26244465 | ||||||
chr1:26244502
|
T | A | 114 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(111): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.208+184T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26244502 | ||||||
chr1:26244601
|
G | A | 84 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0003g0003others(81): Show | 86 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+283G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26244601 | ||||||
chr1:26244714
|
C | T | 1 | a0002c0002t0001g0286 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.208+396C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26244714 | ||||||
chr1:26244992
|
C | T | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.208+674C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26244992 | ||||||
chr1:26244999
|
A | G | 1 | a0002c0002t0010g0283 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.208+681A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26244999 | ||||||
chr1:26245187
|
A | AT | 193 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(190): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.208+883dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26245187 | |||||
chr1:26245187
|
A | ATT | 8 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0003g0097others(5): Show | 8 | HG01167.hp2 HG02723.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+882_208+883dup others(2): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26245187 | |||||
chr1:26245187
|
AT | A | 30 | a0001c0001t0001g0315a0001c0001t0002g0085a0003c0003t0004g0300others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.208+883delT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26245187 | |||||
chr1:26245202
|
C | T | 1 | a0001c0001t0003g0162 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.208+884C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245202 | ||||||
chr1:26245203
|
A | C | 1 | a0001c0001t0003g0162 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.208+885A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245203 | ||||||
chr1:26245204
|
T | A | 1 | a0001c0001t0003g0162 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.208+886T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245204 | ||||||
chr1:26245320
|
A | G | 232 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.208+1002A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245320 | ||||||
chr1:26245360
|
C | T | 1 | a0001c0001t0002g0013 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.208+1042C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245360 | ||||||
chr1:26245463
|
C | T | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.208+1145C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245463 | ||||||
chr1:26245484
|
A | G | 72 | a0001c0001t0003g0003a0001c0001t0003g0092a0001c0001t0003g0098others(69): Show | 74 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.208+1166A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245484 | ||||||
chr1:26245486
|
G | A | 232 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.208+1168G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245486 | ||||||
chr1:26245738
|
C | T | 9 | a0001c0001t0001g0284a0001c0001t0001g0285a0004c0004t0003g0292others(6): Show | 9 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.208+1420C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245738 | ||||||
chr1:26245910
|
C | A | 1 | a0002c0002t0001g0224 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.208+1592C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245910 | ||||||
chr1:26245979
|
C | CA | 119 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(116): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.208+1672dupA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26245979 | |||||
chr1:26246141
|
A | G | 10 | a0002c0002t0001g0219a0002c0002t0001g0220a0002c0002t0001g0255others(7): Show | 10 | NA18954.hp1 NA18968.hp2 NA18971.hp1 others(7): Show |
intron_variant | MODIFIER | c.208+1823A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26246141 | ||||||
chr1:26246220
|
C | T | 1 | a0002c0002t0001g0254 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.208+1902C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26246220 | ||||||
chr1:26246301
|
T | A | 1 | a0001c0001t0002g0039 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.208+1983T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26246301 | ||||||
chr1:26246477
|
T | C | 2 | a0003c0005t0004g0322a0003c0005t0004g0323 | 2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.208+2159T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26246477 | ||||||
chr1:26246532
|
G | A | 29 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.208+2214G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26246532 | ||||||
chr1:26246726
|
CT | C | 66 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.208+2411delT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26246726 | |||||
chr1:26246728
|
TTA | T | 6 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(3): Show | 6 | HG01071.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+2411_208+2412d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26246728 | ||||||
chr1:26246729
|
T | A | 76 | a0001c0001t0001g0248a0001c0001t0001g0266a0001c0001t0001g0269others(73): Show | 79 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.208+2411T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26246729 | ||||||
chr1:26247150
|
T | C | 9 | a0001c0001t0001g0284a0001c0001t0001g0285a0004c0004t0003g0292others(6): Show | 9 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.208+2832T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26247150 | ||||||
chr1:26247476
|
T | C | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.208+3158T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26247476 | ||||||
chr1:26247767
|
A | G | 232 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.208+3449A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26247767 | ||||||
chr1:26247786
|
C | T | 10 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0016t0011g0324others(7): Show | 10 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.208+3468C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26247786 | ||||||
chr1:26247839
|
G | A | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.208+3521G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26247839 | ||||||
chr1:26247941
|
G | T | 73 | a0001c0001t0003g0003a0001c0001t0003g0092a0001c0001t0003g0097others(70): Show | 75 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.208+3623G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26247941 | ||||||
chr1:26248067
|
A | G | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.208+3749A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248067 | ||||||
chr1:26248168
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.208+3850C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248168 | ||||||
chr1:26248175
|
T | C | 2 | a0003c0005t0004g0322a0003c0005t0004g0323 | 2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.208+3857T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248175 | ||||||
chr1:26248176
|
G | A | 2 | a0003c0005t0004g0322a0003c0005t0004g0323 | 2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.208+3858G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248176 | ||||||
chr1:26248177
|
T | G | 2 | a0003c0005t0004g0322a0003c0005t0004g0323 | 2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.208+3859T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248177 | ||||||
chr1:26248325
|
C | A | 1 | a0001c0001t0002g0086 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.208+4007C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248325 | ||||||
chr1:26248478
|
T | C | 1 | a0001c0001t0002g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.208+4160T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248478 | ||||||
chr1:26248549
|
G | A | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.208+4231G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248549 | ||||||
chr1:26248677
|
G | T | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.208+4359G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248677 | ||||||
chr1:26248722
|
C | CTT | 17 | a0001c0001t0001g0179a0001c0001t0001g0298a0001c0001t0001g0299others(14): Show | 17 | HG00544.hp1 HG01167.hp2 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.208+4425_208+4426d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTT | 104 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(101): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.208+4424_208+4426d others(5): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTT | 10 | a0001c0001t0001g0206a0001c0001t0001g0211a0002c0002t0001g0223others(7): Show | 10 | HG00438.hp1 HG00621.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.208+4423_208+4426d others(6): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTT | 22 | a0003c0003t0004g0300a0003c0003t0004g0302a0003c0003t0004g0303others(19): Show | 22 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.208+4422_208+4426d others(7): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTT | 8 | a0001c0001t0001g0315a0001c0001t0003g0107a0003c0003t0004g0307others(5): Show | 8 | HG00323.hp2 HG00741.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+4421_208+4426d others(8): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT | 9 | a0001c0001t0003g0098a0001c0001t0003g0104a0001c0001t0003g0109others(6): Show | 9 | HG02258.hp2 HG02486.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.208+4420_208+4426d others(9): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(1): Show |
7 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0003g0117others(4): Show | 7 | HG01891.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+4419_208+4426d others(10): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(2): Show |
6 | a0001c0001t0003g0097a0001c0001t0003g0113a0004c0004t0003g0292others(3): Show | 6 | HG01106.hp2 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+4418_208+4426d others(11): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(3): Show |
5 | a0001c0001t0003g0003a0001c0001t0003g0092a0001c0001t0003g0120others(2): Show | 7 | HG00639.hp1 HG00733.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+4417_208+4426d others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0003g0122a0001c0001t0003g0143 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.208+4416_208+4426d others(13): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0003g0099a0001c0001t0003g0151a0006c0018t0003g0123 | 3 | HG01192.hp2 HG03139.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.208+4414_208+4426d others(15): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(7): Show |
5 | a0001c0001t0003g0100a0001c0001t0003g0101a0001c0001t0003g0114others(2): Show | 5 | HG00639.hp2 HG01099.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+4413_208+4426d others(16): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0003g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.208+4412_208+4426d others(17): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(9): Show |
2 | a0001c0001t0003g0118a0001c0001t0003g0147 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.208+4411_208+4426d others(18): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0003g0124 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.208+4410_208+4426d others(19): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(11): Show |
2 | a0001c0001t0003g0125a0001c0001t0003g0135 | 2 | HG03017.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.208+4409_208+4426d others(20): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(12): Show |
2 | a0001c0001t0003g0106a0001c0001t0003g0110 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.208+4408_208+4426d others(21): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(13): Show |
3 | a0001c0001t0003g0126a0001c0001t0003g0141a0001c0001t0003g0152 | 3 | HG01952.hp1 HG04199.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.208+4407_208+4426d others(22): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(14): Show |
2 | a0001c0001t0003g0158a0001c0001t0003g0164 | 2 | NA19012.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.208+4406_208+4426d others(23): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(15): Show |
6 | a0001c0001t0003g0119a0001c0001t0003g0127a0001c0001t0003g0128others(3): Show | 6 | NA18943.hp2 NA18949.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+4405_208+4426d others(24): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0003g0132 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.208+4426_208+4427i others(28): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0003g0133 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.208+4426_208+4427i others(29): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(21): Show |
3 | a0001c0001t0003g0103a0001c0001t0003g0134a0001c0001t0003g0144 | 3 | HG01074.hp2 HG01358.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.208+4426_208+4427i others(30): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(23): Show |
1 | a0001c0001t0003g0145 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.208+4426_208+4427i others(32): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(27): Show |
1 | a0001c0001t0003g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.208+4426_208+4427i others(36): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(33): Show |
1 | a0001c0009t0003g0108 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.208+4426_208+4427i others(42): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248722
|
C | CTTTTTTT others(37): Show |
1 | a0001c0009t0003g0111 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.208+4426_208+4427i others(46): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | |||||
chr1:26248927
|
C | T | 5 | a0004c0004t0003g0292a0004c0004t0003g0295a0004c0004t0008g0293others(2): Show | 5 | HG00639.hp1 HG02257.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+4609C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248927 | ||||||
chr1:26248990
|
T | C | 1 | a0001c0001t0005g0017 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.208+4672T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248990 | ||||||
chr1:26249032
|
A | G | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.208+4714A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249032 | ||||||
chr1:26249087
|
G | A | 2 | a0001c0001t0005g0018a0001c0001t0005g0019 | 2 | HG00642.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.208+4769G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249087 | ||||||
chr1:26249167
|
C | T | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.208+4849C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249167 | ||||||
chr1:26249186
|
A | T | 1 | a0001c0001t0003g0131 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.208+4868A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249186 | ||||||
chr1:26249204
|
T | C | 232 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.208+4886T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249204 | ||||||
chr1:26249225
|
G | A | 1 | a0004c0010t0003g0290 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.208+4907G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249225 | ||||||
chr1:26249238
|
C | T | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG01167.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.208+4920C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249238 | ||||||
chr1:26249343
|
A | G | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.208+5025A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249343 | ||||||
chr1:26249386
|
A | G | 1 | a0001c0001t0003g0118 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.208+5068A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249386 | ||||||
chr1:26249448
|
G | A | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.208+5130G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249448 | ||||||
chr1:26249481
|
C | A | 1 | a0001c0001t0003g0098 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.208+5163C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249481 | ||||||
chr1:26249490
|
T | C | 2 | a0001c0001t0003g0158a0001c0001t0003g0164 | 2 | NA19012.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.208+5172T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249490 | ||||||
chr1:26249528
|
G | T | 1 | a0001c0001t0002g0069 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.208+5210G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249528 | ||||||
chr1:26249541
|
A | G | 232 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.208+5223A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249541 | ||||||
chr1:26249756
|
T | G | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.209-5415T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249756 | ||||||
chr1:26249953
|
A | G | 7 | a0004c0004t0003g0292a0004c0004t0003g0295a0004c0004t0003g0296others(4): Show | 7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-5218A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249953 | ||||||
chr1:26250165
|
CAG | C | 72 | a0001c0001t0003g0003a0001c0001t0003g0092a0001c0001t0003g0098others(69): Show | 74 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.209-5003_209-5002d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250165 | |||||
chr1:26250775
|
T | C | 1 | a0001c0001t0003g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.209-4396T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250775 | ||||||
chr1:26250847
|
C | T | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.209-4324C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250847 | ||||||
chr1:26250893
|
A | G | 2 | a0003c0003t0004g0310a0003c0003t0004g0317 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.209-4278A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250893 | ||||||
chr1:26250925
|
C | CCTTTTTT others(7): Show |
1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.209-4246_209-4245i others(16): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250925 | ||||||
chr1:26250925
|
C | CT | 6 | a0001c0001t0001g0285a0001c0001t0002g0061a0001c0001t0002g0062others(3): Show | 6 | HG00558.hp1 HG01891.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-4240dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | |||||
chr1:26250925
|
C | CTT | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(2): Show | 5 | HG00438.hp2 HG01192.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-4241_209-4240d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | |||||
chr1:26250925
|
C | CTTT | 5 | a0001c0001t0001g0284a0001c0001t0002g0038a0001c0001t0002g0068others(2): Show | 5 | HG02723.hp1 NA18906.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-4242_209-4240d others(5): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | |||||
chr1:26250925
|
CTTTTTTC others(1): Show |
C | 6 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(3): Show | 6 | HG00597.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-4239_209-4232d others(10): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | |||||
chr1:26250925
|
CTTTTTTC others(2): Show |
C | 6 | a0003c0003t0004g0316a0003c0003t0006g0093a0003c0003t0006g0094others(3): Show | 6 | HG00280.hp2 HG00733.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-4239_209-4231d others(11): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | |||||
chr1:26250925
|
CTTTTTTC others(3): Show |
C | 22 | a0001c0001t0001g0315a0001c0016t0011g0324a0003c0003t0004g0300others(19): Show | 22 | HG00140.hp2 HG00323.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.209-4239_209-4230d others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | |||||
chr1:26250925
|
CTTTTTTC others(4): Show |
C | 5 | a0001c0001t0003g0003a0001c0001t0003g0101a0001c0001t0003g0121others(2): Show | 7 | HG00733.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-4239_209-4229d others(13): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | |||||
chr1:26250925
|
CTTTTTTC others(5): Show |
C | 65 | a0001c0001t0003g0092a0001c0001t0003g0098a0001c0001t0003g0099others(62): Show | 65 | HG00544.hp1 HG00639.hp2 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.209-4239_209-4228d others(14): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | |||||
chr1:26250925
|
CTTTTTTC others(6): Show |
C | 2 | a0001c0001t0003g0107a0001c0001t0003g0153 | 2 | HG00323.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.209-4239_209-4227d others(15): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | |||||
chr1:26250925
|
CTTTTTTC others(9): Show |
C | 1 | a0001c0001t0002g0040 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.209-4239_209-4224d others(18): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | |||||
chr1:26250928
|
T | C | 1 | a0002c0002t0007g0213 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.209-4243T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250928 | ||||||
chr1:26250928
|
TTTTC | T | 10 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(7): Show | 10 | HG00639.hp1 HG01071.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.209-4239_209-4236d others(6): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250928 | |||||
chr1:26250929
|
TTTC | T | 109 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(106): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.209-4239_209-4237d others(5): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250929 | |||||
chr1:26250931
|
TC | T | 45 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(42): Show | 54 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.209-4239delC | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250931 | ||||||
chr1:26250932
|
C | T | 46 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0032others(43): Show | 46 | HG00438.hp2 HG00558.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.209-4239C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250932 | ||||||
chr1:26250936
|
T | C | 2 | a0001c0001t0002g0087a0001c0001t0002g0090 | 2 | HG00621.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.209-4235T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250936 | ||||||
chr1:26250940
|
T | C | 3 | a0001c0001t0001g0179a0002c0002t0001g0252a0002c0002t0001g0255 | 3 | HG02280.hp1 NA19067.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.209-4231T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250940 | ||||||
chr1:26250941
|
T | C | 114 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(111): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.209-4230T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250941 | ||||||
chr1:26250942
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.209-4229T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250942 | ||||||
chr1:26251028
|
G | A | 84 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0003g0003others(81): Show | 86 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.209-4143G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251028 | ||||||
chr1:26251091
|
C | T | 10 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0016t0011g0324others(7): Show | 10 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.209-4080C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251091 | ||||||
chr1:26251251
|
G | GT | 119 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(116): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.209-3903dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26251251 | |||||
chr1:26251251
|
G | GTT | 18 | a0001c0001t0001g0191a0001c0001t0001g0284a0001c0001t0001g0285others(15): Show | 18 | HG00639.hp1 HG01358.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.209-3904_209-3903d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26251251 | |||||
chr1:26251257
|
T | TG | 72 | a0001c0001t0003g0003a0001c0001t0003g0092a0001c0001t0003g0098others(69): Show | 74 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.209-3914_209-3913i others(3): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251257 | ||||||
chr1:26251300
|
G | A | 2 | a0002c0002t0001g0226a0002c0002t0001g0263 | 2 | HG00280.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.209-3871G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251300 | ||||||
chr1:26251321
|
G | A | 3 | a0005c0006t0001g0260a0005c0006t0001g0261a0005c0006t0001g0278 | 3 | HG02630.hp2 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.209-3850G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251321 | ||||||
chr1:26251494
|
G | A | 32 | a0001c0001t0001g0315a0001c0001t0002g0041a0001c0001t0002g0071others(29): Show | 32 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.209-3677G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251494 | ||||||
chr1:26251649
|
A | G | 1 | a0002c0002t0001g0219 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-3522A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251649 | ||||||
chr1:26251742
|
G | A | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.209-3429G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251742 | ||||||
chr1:26251852
|
A | T | 1 | a0002c0002t0001g0270 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.209-3319A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251852 | ||||||
chr1:26251943
|
T | C | 1 | a0003c0005t0004g0297 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.209-3228T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251943 | ||||||
chr1:26252036
|
C | T | 118 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(115): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.209-3135C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252036 | ||||||
chr1:26252123
|
C | T | 1 | a0001c0001t0003g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.209-3048C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252123 | ||||||
chr1:26252185
|
C | G | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.209-2986C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252185 | ||||||
chr1:26252251
|
G | T | 5 | a0003c0003t0004g0302a0003c0003t0004g0310a0003c0003t0004g0311others(2): Show | 5 | HG00140.hp2 HG00323.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-2920G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252251 | ||||||
chr1:26252258
|
G | C | 5 | a0004c0004t0003g0292a0004c0004t0003g0295a0004c0004t0008g0293others(2): Show | 5 | HG00639.hp1 HG02257.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-2913G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252258 | ||||||
chr1:26252307
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.209-2864C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252307 | ||||||
chr1:26252314
|
C | T | 113 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(110): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.209-2857C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252314 | ||||||
chr1:26252341
|
TGACCA | T | 2 | a0001c0001t0002g0006a0001c0001t0002g0052 | 3 | NA18968.hp1 NA19057.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.209-2828_209-2824d others(7): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26252341 | |||||
chr1:26252487
|
G | A | 1 | a0001c0001t0002g0042 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.209-2684G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252487 | ||||||
chr1:26252489
|
G | A | 84 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0003g0003others(81): Show | 86 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.209-2682G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252489 | ||||||
chr1:26252512
|
A | G | 1 | a0001c0001t0003g0130 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.209-2659A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252512 | ||||||
chr1:26252732
|
C | T | 232 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.209-2439C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252732 | ||||||
chr1:26252915
|
C | T | 10 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0016t0011g0324others(7): Show | 10 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.209-2256C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252915 | ||||||
chr1:26252929
|
A | G | 1 | a0001c0001t0002g0074 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.209-2242A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252929 | ||||||
chr1:26252995
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.209-2176G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252995 | ||||||
chr1:26253070
|
T | C | 84 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0003g0003others(81): Show | 86 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.209-2101T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253070 | ||||||
chr1:26253145
|
A | G | 10 | a0001c0001t0003g0119a0001c0001t0003g0126a0001c0001t0003g0127others(7): Show | 10 | HG01358.hp2 HG01952.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.209-2026A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253145 | ||||||
chr1:26253156
|
A | G | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.209-2015A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253156 | ||||||
chr1:26253390
|
C | CT | 10 | a0001c0001t0001g0179a0001c0001t0002g0059a0001c0001t0003g0156others(7): Show | 10 | HG00438.hp1 HG00544.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.209-1764dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26253390 | |||||
chr1:26253390
|
C | CTT | 25 | a0001c0001t0001g0315a0003c0003t0004g0301a0003c0003t0004g0302others(22): Show | 25 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.209-1765_209-1764d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26253390 | |||||
chr1:26253590
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.209-1581C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253590 | ||||||
chr1:26253683
|
C | T | 1 | a0002c0002t0001g0219 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1488C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253683 | ||||||
chr1:26253685
|
C | T | 1 | a0002c0002t0001g0219 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1486C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253685 | ||||||
chr1:26253688
|
C | T | 1 | a0002c0002t0001g0219 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1483C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253688 | ||||||
chr1:26253689
|
C | G | 1 | a0002c0002t0001g0219 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1482C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253689 | ||||||
chr1:26253690
|
T | C | 1 | a0002c0002t0001g0219 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1481T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253690 | ||||||
chr1:26253692
|
A | G | 1 | a0002c0002t0001g0219 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1479A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253692 | ||||||
chr1:26253694
|
C | G | 1 | a0002c0002t0001g0219 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1477C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253694 | ||||||
chr1:26253695
|
T | A | 1 | a0002c0002t0001g0219 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1476T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253695 | ||||||
chr1:26253697
|
T | A | 1 | a0002c0002t0001g0219 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1474T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253697 | ||||||
chr1:26253698
|
T | A | 1 | a0002c0002t0001g0219 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1473T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253698 | ||||||
chr1:26253699
|
T | A | 1 | a0002c0002t0001g0219 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1472T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253699 | ||||||
chr1:26253705
|
T | A | 1 | a0002c0002t0001g0219 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1466T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253705 | ||||||
chr1:26253839
|
C | T | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.209-1332C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253839 | ||||||
chr1:26253871
|
A | G | 1 | a0003c0003t0004g0314 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.209-1300A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253871 | ||||||
chr1:26253927
|
C | T | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.209-1244C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253927 | ||||||
chr1:26254299
|
C | T | 12 | a0001c0001t0001g0169a0001c0001t0001g0201a0001c0001t0001g0202others(9): Show | 12 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.209-872C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26254299 | ||||||
chr1:26254336
|
T | C | 2 | a0003c0005t0004g0322a0003c0005t0004g0323 | 2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.209-835T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26254336 | ||||||
chr1:26254393
|
C | T | 1 | a0002c0002t0001g0247 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.209-778C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26254393 | ||||||
chr1:26254427
|
T | TA | 31 | a0001c0001t0001g0315a0001c0001t0002g0032a0001c0001t0003g0158others(28): Show | 31 | HG00140.hp2 HG00323.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.209-731dupA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26254427 | |||||
chr1:26254439
|
A | C | 1 | a0001c0001t0002g0051 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.209-732A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26254439 | ||||||
chr1:26254446
|
T | G | 113 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(110): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.209-725T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26254446 | ||||||
chr1:26254667
|
G | A | 1 | a0002c0002t0001g0282 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.209-504G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26254667 | ||||||
chr1:26254864
|
T | A | 5 | a0003c0005t0004g0297a0003c0005t0004g0322a0003c0005t0004g0323others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-307T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26254864 | ||||||
chr1:26254920
|
A | G | 1 | a0002c0002t0001g0246 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.209-251A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26254920 | ||||||
chr1:26256073
|
A | G | 1 | a0003c0003t0004g0307 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.903+208A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256073 | ||||||
chr1:26256195
|
T | A | 84 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0003g0003others(81): Show | 86 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.903+330T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256195 | ||||||
chr1:26256204
|
A | G | 1 | a0001c0001t0002g0037 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.903+339A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256204 | ||||||
chr1:26256220
|
G | A | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.903+355G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256220 | ||||||
chr1:26256222
|
C | T | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.903+357C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256222 | ||||||
chr1:26256335
|
A | C | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG01167.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.903+470A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256335 | ||||||
chr1:26256596
|
T | TTTTC | 4 | a0003c0003t0004g0310a0003c0003t0004g0316a0003c0003t0004g0317others(1): Show | 4 | HG01516.hp2 HG01517.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.903+735_903+738dup others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256596 | |||||
chr1:26256600
|
C | CT | 6 | a0001c0001t0001g0190a0001c0001t0001g0205a0001c0001t0002g0037others(3): Show | 6 | HG00438.hp2 HG02056.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.903+751dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256600 | |||||
chr1:26256600
|
CTT | C | 80 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0003g0003others(77): Show | 82 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.903+750_903+751del others(2): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256600 | |||||
chr1:26256601
|
T | TTTC | 25 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(22): Show | 25 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.903+738_903+739ins others(3): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256601 | |||||
chr1:26256735
|
A | G | 7 | a0002c0002t0001g0224a0002c0002t0001g0243a0002c0002t0001g0244others(4): Show | 7 | HG00621.hp2 HG02132.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.904-862A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256735 | ||||||
chr1:26256746
|
G | A | 5 | a0001c0001t0001g0177a0001c0001t0001g0190a0001c0001t0001g0191others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.904-851G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256746 | ||||||
chr1:26256808
|
C | T | 1 | a0001c0001t0003g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.904-789C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256808 | ||||||
chr1:26256924
|
T | G | 118 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(115): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.904-673T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256924 | ||||||
chr1:26256926
|
T | G | 118 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(115): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.904-671T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256926 | ||||||
chr1:26256928
|
G | GGGGTGTG others(3): Show |
6 | a0004c0004t0003g0292a0004c0004t0003g0295a0004c0004t0008g0293others(3): Show | 6 | HG00639.hp1 HG02257.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.904-668_904-667ins others(10): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | |||||
chr1:26256928
|
G | GGGGTGTG others(7): Show |
2 | a0003c0005t0004g0322a0003c0005t0004g0323 | 2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.904-668_904-667ins others(14): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | |||||
chr1:26256928
|
G | GGGGTGTG others(9): Show |
3 | a0001c0001t0012g0168a0003c0005t0004g0297a0003c0007t0004g0321 | 3 | HG02486.hp1 HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.904-668_904-667ins others(16): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | |||||
chr1:26256928
|
G | GGGGTGTG others(11): Show |
1 | a0001c0001t0001g0284 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.904-668_904-667ins others(18): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | |||||
chr1:26256928
|
G | GGGGTGTG others(13): Show |
1 | a0001c0001t0001g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.904-668_904-667ins others(20): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | |||||
chr1:26256928
|
G | GGT | 80 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(77): Show | 89 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.904-642_904-641dup others(2): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | |||||
chr1:26256928
|
G | GGTGT | 5 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0059others(2): Show | 5 | HG01934.hp2 HG02071.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.904-644_904-641dup others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | |||||
chr1:26256928
|
G | GGTGTGTG others(5): Show |
1 | a0001c0001t0003g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.904-652_904-641dup others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | |||||
chr1:26256928
|
G | GGTGTGTG others(7): Show |
24 | a0001c0001t0001g0315a0001c0001t0003g0153a0001c0001t0003g0155others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.904-654_904-641dup others(14): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | |||||
chr1:26256928
|
G | GGTGTGTG others(9): Show |
36 | a0001c0001t0003g0100a0001c0001t0003g0101a0001c0001t0003g0102others(33): Show | 36 | HG00544.hp1 HG00639.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.904-656_904-641dup others(16): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | |||||
chr1:26256928
|
G | GGTGTGTG others(11): Show |
22 | a0001c0001t0003g0003a0001c0001t0003g0098a0001c0001t0003g0103others(19): Show | 24 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.904-658_904-641dup others(18): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | |||||
chr1:26256928
|
G | GGTGTGTG others(13): Show |
5 | a0001c0001t0003g0107a0001c0001t0003g0127a0001c0001t0003g0129others(2): Show | 5 | HG00323.hp2 HG02818.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.904-660_904-641dup others(20): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | |||||
chr1:26256928
|
G | GGTGTGTG others(15): Show |
3 | a0001c0001t0003g0097a0001c0016t0011g0324a0003c0003t0004g0319 | 3 | HG02683.hp2 HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.904-662_904-641dup others(22): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | |||||
chr1:26256928
|
G | GTGTGTGT | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG03491.hp2 HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.904-669_904-668ins others(7): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256928 | ||||||
chr1:26256928
|
G | GTGTGTGT others(4): Show |
28 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(25): Show | 28 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.904-669_904-668ins others(11): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256928 | ||||||
chr1:26256928
|
G | GTGTGTGT others(6): Show |
24 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0190others(21): Show | 24 | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.904-669_904-668ins others(13): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256928 | ||||||
chr1:26256928
|
G | GTGTGTGT others(8): Show |
40 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(37): Show | 41 | HG00140.hp1 HG00609.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.904-669_904-668ins others(15): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256928 | ||||||
chr1:26256928
|
G | GTGTGTGT others(10): Show |
16 | a0001c0001t0001g0180a0001c0001t0001g0299a0002c0002t0001g0009others(13): Show | 17 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.904-669_904-668ins others(17): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256928 | ||||||
chr1:26256928
|
G | GTGTGTGT others(12): Show |
2 | a0002c0002t0001g0215a0002c0002t0001g0229 | 2 | HG01433.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.904-669_904-668ins others(19): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256928 | ||||||
chr1:26256928
|
G | GTGTGTGT others(14): Show |
2 | a0001c0001t0001g0298a0002c0002t0001g0228 | 2 | NA19079.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.904-669_904-668ins others(21): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256928 | ||||||
chr1:26256928
|
G | GTGTGTGT others(16): Show |
1 | a0002c0002t0001g0252 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.904-669_904-668ins others(23): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256928 | ||||||
chr1:26256930
|
T | G | 1 | a0003c0007t0004g0320 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.904-667T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256930 | ||||||
chr1:26256955
|
G | GTGTGTGT others(6): Show |
1 | a0001c0001t0003g0145 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.904-641_904-640ins others(13): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256955 | |||||
chr1:26256956
|
T | TG | 4 | a0001c0001t0001g0203a0001c0001t0001g0207a0002c0002t0001g0243others(1): Show | 4 | HG00642.hp1 HG02647.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.904-641_904-640ins others(1): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256956 | ||||||
chr1:26256956
|
T | TGTGTGTG others(10): Show |
5 | a0001c0001t0003g0099a0001c0001t0003g0115a0001c0001t0003g0136others(2): Show | 5 | HG02647.hp1 HG03098.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.904-641_904-640ins others(17): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256956 | ||||||
chr1:26256981
|
C | T | 1 | a0001c0001t0005g0022 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.904-616C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256981 | ||||||
chr1:26257076
|
G | A | 1 | a0001c0001t0002g0005 | 2 | NA18970.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.904-521G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257076 | ||||||
chr1:26257087
|
C | T | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.904-510C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257087 | ||||||
chr1:26257122
|
G | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG00642.hp1 HG00738.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.904-475G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257122 | ||||||
chr1:26257169
|
G | A | 73 | a0001c0001t0003g0003a0001c0001t0003g0092a0001c0001t0003g0097others(70): Show | 75 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.904-428G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257169 | ||||||
chr1:26257190
|
T | C | 232 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.904-407T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257190 | ||||||
chr1:26257213
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.904-384G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257213 | ||||||
chr1:26257360
|
A | G | 7 | a0004c0004t0003g0292a0004c0004t0003g0295a0004c0004t0003g0296others(4): Show | 7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.904-237A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257360 | ||||||
chr1:26257377
|
A | C | 10 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0016t0011g0324others(7): Show | 10 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.904-220A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257377 | ||||||
chr1:26257507
|
T | C | 232 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.904-90T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257507 | ||||||
chr1:26257564
|
G | A | 5 | a0003c0005t0004g0297a0003c0005t0004g0322a0003c0005t0004g0323others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.904-33G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257564 | ||||||
chr1:26257840
|
G | A | 5 | a0003c0005t0004g0297a0003c0005t0004g0322a0003c0005t0004g0323others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037+110G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 5/13 | chr1 | 26257840 | ||||||
chr1:26257860
|
T | C | 7 | a0004c0004t0003g0292a0004c0004t0003g0295a0004c0004t0003g0296others(4): Show | 7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1037+130T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 5/13 | chr1 | 26257860 | ||||||
chr1:26257910
|
G | A | 5 | a0003c0005t0004g0297a0003c0005t0004g0322a0003c0005t0004g0323others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037+180G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 5/13 | chr1 | 26257910 | ||||||
chr1:26258011
|
C | G | 1 | a0001c0001t0001g0315 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1038-132C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 5/13 | chr1 | 26258011 | ||||||
chr1:26258019
|
T | C | 1 | a0002c0002t0001g0226 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1038-124T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 5/13 | chr1 | 26258019 | ||||||
chr1:26258303
|
C | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1155+43C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258303 | ||||||
chr1:26258542
|
TA | T | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1155+284delA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 26258542 | |||||
chr1:26258566
|
A | G | 9 | a0001c0001t0001g0284a0001c0001t0001g0285a0004c0004t0003g0292others(6): Show | 9 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1155+306A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258566 | ||||||
chr1:26258631
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1155+371C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258631 | ||||||
chr1:26258640
|
A | G | 84 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0003g0003others(81): Show | 86 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.1155+380A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258640 | ||||||
chr1:26258683
|
G | A | 3 | a0003c0003t0006g0094a0003c0003t0006g0095a0003c0003t0006g0096 | 3 | HG00280.hp2 HG00733.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1155+423G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258683 | ||||||
chr1:26258685
|
C | T | 15 | a0001c0001t0005g0002a0001c0001t0005g0015a0001c0001t0005g0016others(12): Show | 17 | HG00642.hp2 HG00738.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1155+425C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258685 | ||||||
chr1:26258752
|
A | T | 1 | a0001c0016t0011g0324 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1155+492A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258752 | ||||||
chr1:26258754
|
G | C | 2 | a0001c0001t0002g0039a0001c0001t0002g0089 | 2 | NA18940.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1155+494G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258754 | ||||||
chr1:26258799
|
G | T | 8 | a0001c0001t0003g0092a0001c0001t0003g0105a0001c0001t0003g0120others(5): Show | 8 | HG03831.hp2 HG03834.hp2 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.1155+539G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258799 | ||||||
chr1:26258891
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1155+631G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258891 | ||||||
chr1:26258892
|
G | C | 1 | a0001c0001t0003g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1155+632G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258892 | ||||||
chr1:26259166
|
G | T | 118 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(115): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.1156-451G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26259166 | ||||||
chr1:26259265
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1156-352C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26259265 | ||||||
chr1:26259283
|
A | G | 1 | a0002c0002t0001g0242 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1156-334A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26259283 | ||||||
chr1:26259351
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1156-266G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26259351 | ||||||
chr1:26259504
|
A | G | 1 | a0001c0001t0003g0120 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1156-113A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26259504 | ||||||
chr1:26259590
|
G | A | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1156-27G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26259590 | ||||||
chr1:26259869
|
T | A | 1 | a0001c0001t0001g0315 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1341+67T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26259869 | ||||||
chr1:26259894
|
G | C | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1341+92G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26259894 | ||||||
chr1:26259927
|
T | A | 1 | a0004c0004t0003g0292 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1341+125T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26259927 | ||||||
chr1:26260112
|
T | C | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1341+310T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26260112 | ||||||
chr1:26260320
|
G | A | 1 | a0001c0001t0003g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1341+518G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26260320 | ||||||
chr1:26260501
|
G | GA | 118 | a0001c0001t0001g0207a0001c0001t0001g0214a0001c0001t0001g0315others(115): Show | 127 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1341+713dupA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26260501 | |||||
chr1:26260520
|
A | T | 2 | a0003c0003t0004g0303a0003c0003t0004g0325 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1341+718A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26260520 | ||||||
chr1:26260547
|
A | T | 231 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(228): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1341+745A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26260547 | ||||||
chr1:26260664
|
A | G | 1 | a0001c0001t0001g0299 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1341+862A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26260664 | ||||||
chr1:26261416
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1341+1614G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261416 | ||||||
chr1:26261426
|
C | T | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1341+1624C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261426 | ||||||
chr1:26261427
|
G | A | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1341+1625G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261427 | ||||||
chr1:26261567
|
T | C | 1 | a0003c0003t0006g0094 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1341+1765T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261567 | ||||||
chr1:26261630
|
C | G | 2 | a0002c0002t0001g0233a0002c0002t0001g0274 | 2 | HG00099.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1341+1828C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261630 | ||||||
chr1:26261720
|
C | CTCTT | 147 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(144): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.1341+1921_1341+192 others(8): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26261720 | |||||
chr1:26261724
|
C | T | 1 | a0001c0001t0001g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1341+1922C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261724 | ||||||
chr1:26261726
|
TA | T | 6 | a0001c0001t0002g0037a0001c0001t0002g0052a0001c0001t0002g0058others(3): Show | 6 | HG01975.hp2 HG02723.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.1341+1939delA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26261726 | |||||
chr1:26261727
|
A | T | 1 | a0001c0001t0001g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1341+1925A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261727 | ||||||
chr1:26261741
|
AT | A | 188 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(185): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1341+1949delT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26261741 | |||||
chr1:26261742
|
T | A | 41 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0315others(38): Show | 41 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.1341+1940T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261742 | ||||||
chr1:26261743
|
T | A | 89 | a0001c0001t0001g0177a0001c0001t0001g0188a0001c0001t0001g0189others(86): Show | 91 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.1341+1941T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261743 | ||||||
chr1:26261773
|
T | C | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1341+1971T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261773 | ||||||
chr1:26261817
|
A | C | 1 | a0004c0010t0003g0290 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1341+2015A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261817 | ||||||
chr1:26262180
|
G | A | 72 | a0001c0001t0003g0003a0001c0001t0003g0092a0001c0001t0003g0098others(69): Show | 74 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1341+2378G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262180 | ||||||
chr1:26262239
|
G | A | 118 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(115): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.1341+2437G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262239 | ||||||
chr1:26262263
|
C | T | 1 | a0001c0001t0003g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1341+2461C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262263 | ||||||
chr1:26262300
|
C | G | 2 | a0002c0002t0001g0271a0002c0002t0001g0276 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1341+2498C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262300 | ||||||
chr1:26262306
|
C | CA | 35 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.1341+2513dupA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26262306 | |||||
chr1:26262335
|
G | A | 73 | a0001c0001t0003g0003a0001c0001t0003g0092a0001c0001t0003g0097others(70): Show | 75 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.1341+2533G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262335 | ||||||
chr1:26262407
|
G | A | 1 | a0001c0016t0011g0324 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1341+2605G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262407 | ||||||
chr1:26262417
|
G | A | 1 | a0001c0001t0005g0022 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1341+2615G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262417 | ||||||
chr1:26262419
|
A | C | 1 | a0001c0001t0001g0189 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1341+2617A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262419 | ||||||
chr1:26262510
|
C | T | 1 | a0001c0001t0005g0017 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1341+2708C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262510 | ||||||
chr1:26262535
|
G | A | 1 | a0006c0018t0003g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1341+2733G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262535 | ||||||
chr1:26262561
|
G | T | 73 | a0001c0001t0003g0003a0001c0001t0003g0092a0001c0001t0003g0097others(70): Show | 75 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.1341+2759G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262561 | ||||||
chr1:26262882
|
A | G | 232 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1341+3080A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262882 | ||||||
chr1:26262938
|
T | C | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1341+3136T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262938 | ||||||
chr1:26263145
|
A | G | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1341+3343A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263145 | ||||||
chr1:26263207
|
T | A | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1341+3405T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263207 | ||||||
chr1:26263459
|
A | T | 9 | a0001c0001t0001g0284a0001c0001t0001g0285a0004c0004t0003g0292others(6): Show | 9 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1341+3657A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263459 | ||||||
chr1:26263496
|
C | T | 1 | a0001c0001t0002g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1341+3694C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263496 | ||||||
chr1:26263617
|
G | A | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1341+3815G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263617 | ||||||
chr1:26263631
|
A | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG00642.hp1 HG00738.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1341+3829A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263631 | ||||||
chr1:26263691
|
G | A | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1341+3889G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263691 | ||||||
chr1:26263753
|
C | A | 1 | a0001c0001t0002g0060 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1341+3951C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263753 | ||||||
chr1:26263807
|
C | T | 5 | a0003c0005t0004g0297a0003c0005t0004g0322a0003c0005t0004g0323others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1341+4005C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263807 | ||||||
chr1:26263875
|
A | C | 2 | a0003c0003t0006g0094a0003c0003t0006g0095 | 2 | HG00280.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.1341+4073A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263875 | ||||||
chr1:26263941
|
G | A | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1341+4139G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263941 | ||||||
chr1:26263952
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1341+4150G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263952 | ||||||
chr1:26264110
|
A | G | 72 | a0001c0001t0003g0003a0001c0001t0003g0092a0001c0001t0003g0098others(69): Show | 74 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1341+4308A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26264110 | ||||||
chr1:26264685
|
C | A | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1342-3798C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26264685 | ||||||
chr1:26264764
|
A | G | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1342-3719A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26264764 | ||||||
chr1:26264809
|
T | A | 1 | a0001c0016t0011g0324 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1342-3674T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26264809 | ||||||
chr1:26264979
|
G | T | 1 | a0001c0001t0003g0098 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1342-3504G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26264979 | ||||||
chr1:26264980
|
C | CT | 79 | a0001c0001t0001g0177a0001c0001t0001g0186a0001c0001t0001g0188others(76): Show | 80 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.1342-3480dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26264980 | |||||
chr1:26264980
|
C | CTT | 6 | a0001c0001t0001g0179a0001c0001t0001g0189a0001c0001t0001g0191others(3): Show | 6 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1342-3481_1342-348 others(6): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26264980 | |||||
chr1:26264980
|
CT | C | 61 | a0001c0001t0002g0054a0001c0001t0003g0003a0001c0001t0003g0092others(58): Show | 63 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.1342-3480delT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26264980 | |||||
chr1:26265003
|
T | TA | 5 | a0004c0004t0003g0292a0004c0004t0003g0296a0004c0004t0008g0293others(2): Show | 5 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1342-3479dupA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26265003 | |||||
chr1:26265007
|
T | C | 232 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1342-3476T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265007 | ||||||
chr1:26265060
|
T | C | 10 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0016t0011g0324others(7): Show | 10 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1342-3423T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265060 | ||||||
chr1:26265076
|
C | T | 1 | a0004c0004t0003g0292 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1342-3407C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265076 | ||||||
chr1:26265145
|
G | A | 118 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(115): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.1342-3338G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265145 | ||||||
chr1:26265336
|
C | T | 3 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289 | 3 | HG01081.hp1 HG01346.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1342-3147C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265336 | ||||||
chr1:26265550
|
A | G | 1 | a0002c0002t0001g0242 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1342-2933A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265550 | ||||||
chr1:26265565
|
T | C | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1342-2918T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265565 | ||||||
chr1:26265701
|
T | C | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1342-2782T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265701 | ||||||
chr1:26265800
|
C | T | 1 | a0010c0017t0004g0306 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1342-2683C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265800 | ||||||
chr1:26265819
|
C | G | 1 | a0002c0002t0001g0233 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1342-2664C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265819 | ||||||
chr1:26265819
|
C | T | 117 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(114): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1342-2664C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265819 | ||||||
chr1:26265870
|
C | T | 1 | a0001c0016t0011g0324 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1342-2613C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265870 | ||||||
chr1:26266082
|
A | G | 232 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1342-2401A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266082 | ||||||
chr1:26266103
|
G | A | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1342-2380G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266103 | ||||||
chr1:26266143
|
A | G | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1342-2340A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266143 | ||||||
chr1:26266221
|
T | A | 1 | a0001c0001t0001g0199 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1342-2262T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266221 | ||||||
chr1:26266223
|
G | T | 30 | a0001c0001t0001g0315a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1342-2260G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266223 | ||||||
chr1:26266236
|
A | G | 113 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(110): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.1342-2247A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266236 | ||||||
chr1:26266259
|
A | C | 1 | a0004c0010t0003g0290 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1342-2224A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266259 | ||||||
chr1:26266380
|
C | T | 22 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0003t0004g0302others(19): Show | 22 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.1342-2103C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266380 | ||||||
chr1:26266548
|
G | A | 6 | a0001c0001t0003g0106a0001c0001t0003g0109a0001c0001t0003g0110others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1342-1935G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266548 | ||||||
chr1:26266587
|
T | G | 5 | a0001c0001t0001g0177a0001c0001t0001g0190a0001c0001t0001g0191others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1342-1896T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266587 | ||||||
chr1:26266591
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1342-1892A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266591 | ||||||
chr1:26267012
|
T | C | 73 | a0001c0001t0001g0315a0001c0001t0003g0003a0001c0001t0003g0092others(70): Show | 75 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.1342-1471T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26267012 | ||||||
chr1:26267169
|
G | C | 1 | a0003c0003t0004g0313 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1342-1314G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26267169 | ||||||
chr1:26267216
|
TACTC | T | 3 | a0003c0003t0004g0302a0003c0003t0004g0311a0003c0003t0004g0319 | 3 | HG00140.hp2 HG00323.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1342-1264_1342-126 others(8): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26267216 | |||||
chr1:26267273
|
A | G | 2 | a0001c0001t0002g0048a0001c0001t0002g0086 | 2 | NA18951.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1342-1210A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26267273 | ||||||
chr1:26267353
|
CAG | C | 29 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0003t0004g0302others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1342-1129_1342-112 others(6): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26267353 | ||||||
chr1:26267362
|
G | A | 1 | a0001c0016t0011g0324 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1342-1121G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26267362 | ||||||
chr1:26267433
|
G | A | 1 | a0002c0002t0010g0283 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1342-1050G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26267433 | ||||||
chr1:26267502
|
C | T | 1 | a0003c0003t0004g0325 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1342-981C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26267502 | ||||||
chr1:26267719
|
G | A | 3 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0001g0268 | 3 | NA18940.hp2 NA18966.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1342-764G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26267719 | ||||||
chr1:26268109
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1342-374C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26268109 | ||||||
chr1:26268213
|
TTTGGGAG others(3): Show |
T | 1 | a0002c0002t0001g0282 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1342-269_1342-260d others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26268213 | ||||||
chr1:26268445
|
G | A | 1 | a0001c0001t0001g0284 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1342-38G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26268445 | ||||||
chr1:26268773
|
T | C | 1 | a0002c0002t0001g0008 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1494+138T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26268773 | ||||||
chr1:26268777
|
C | T | 1 | a0002c0012t0001g0187 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1494+142C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26268777 | ||||||
chr1:26269015
|
C | T | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG01167.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+380C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26269015 | ||||||
chr1:26269109
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1495-351C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26269109 | ||||||
chr1:26269126
|
C | T | 13 | a0001c0001t0003g0102a0001c0001t0003g0148a0001c0001t0003g0149others(10): Show | 13 | HG00544.hp1 HG02056.hp2 NA18944.hp2 others(10): Show |
intron_variant | MODIFIER | c.1495-334C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26269126 | ||||||
chr1:26269156
|
C | G | 73 | a0001c0001t0001g0315a0001c0001t0003g0003a0001c0001t0003g0092others(70): Show | 75 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.1495-304C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26269156 | ||||||
chr1:26269194
|
T | C | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG03491.hp2 HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1495-266T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26269194 | ||||||
chr1:26269244
|
C | T | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1495-216C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26269244 | ||||||
chr1:26269342
|
C | T | 3 | a0005c0006t0001g0260a0005c0006t0001g0261a0005c0006t0001g0278 | 3 | HG02630.hp2 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1495-118C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26269342 | ||||||
chr1:26269398
|
C | G | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG01167.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1495-62C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26269398 | ||||||
chr1:26269782
|
C | CT | 25 | a0001c0001t0001g0284a0001c0001t0001g0299a0001c0001t0002g0011others(22): Show | 25 | HG00621.hp1 HG01167.hp2 HG01975.hp1 others(22): Show |
intron_variant | MODIFIER | c.1649+190dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 26269782 | |||||
chr1:26269782
|
C | CTT | 59 | a0001c0001t0001g0285a0001c0001t0001g0298a0001c0001t0002g0047others(56): Show | 62 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1649+189_1649+190d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 26269782 | |||||
chr1:26269782
|
C | CTTT | 66 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.1649+188_1649+190d others(5): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 26269782 | |||||
chr1:26269782
|
C | CTTTT | 17 | a0001c0001t0001g0179a0001c0001t0001g0186a0001c0001t0001g0189others(14): Show | 17 | HG00741.hp1 HG01255.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.1649+187_1649+190d others(6): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 26269782 | |||||
chr1:26269782
|
CT | C | 10 | a0001c0001t0003g0098a0001c0001t0003g0099a0001c0001t0003g0136others(7): Show | 10 | HG02258.hp2 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1649+190delT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 26269782 | |||||
chr1:26269849
|
C | G | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1649+235C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26269849 | ||||||
chr1:26269891
|
A | G | 1 | a0001c0016t0011g0324 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1649+277A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26269891 | ||||||
chr1:26269936
|
G | A | 1 | a0001c0001t0003g0145 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1649+322G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26269936 | ||||||
chr1:26269978
|
C | T | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1649+364C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26269978 | ||||||
chr1:26270001
|
C | T | 1 | a0002c0002t0001g0212 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1649+387C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270001 | ||||||
chr1:26270027
|
T | C | 232 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1649+413T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270027 | ||||||
chr1:26270065
|
C | T | 4 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289others(1): Show | 4 | HG01081.hp1 HG01192.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1649+451C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270065 | ||||||
chr1:26270072
|
G | C | 43 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(40): Show | 43 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1649+458G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270072 | ||||||
chr1:26270083
|
G | A | 5 | a0003c0005t0004g0297a0003c0005t0004g0322a0003c0005t0004g0323others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1649+469G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270083 | ||||||
chr1:26270108
|
A | G | 1 | a0001c0001t0002g0033 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1649+494A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270108 | ||||||
chr1:26270123
|
G | A | 22 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0003t0004g0302others(19): Show | 22 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.1649+509G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270123 | ||||||
chr1:26270218
|
G | A | 118 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(115): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.1649+604G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270218 | ||||||
chr1:26270258
|
G | C | 7 | a0004c0004t0003g0292a0004c0004t0003g0295a0004c0004t0003g0296others(4): Show | 7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1649+644G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270258 | ||||||
chr1:26270392
|
A | C | 2 | a0002c0002t0001g0279a0002c0002t0001g0281 | 2 | HG03834.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1650-622A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270392 | ||||||
chr1:26270489
|
T | C | 7 | a0004c0004t0003g0292a0004c0004t0003g0295a0004c0004t0003g0296others(4): Show | 7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1650-525T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270489 | ||||||
chr1:26270586
|
T | C | 5 | a0001c0001t0002g0171a0001c0001t0002g0173a0001c0001t0002g0174others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650-428T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270586 | ||||||
chr1:26270595
|
C | A | 28 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0003t0004g0302others(25): Show | 28 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.1650-419C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270595 | ||||||
chr1:26270653
|
G | A | 118 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(115): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.1650-361G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270653 | ||||||
chr1:26270698
|
G | A | 29 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0003t0004g0302others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1650-316G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270698 | ||||||
chr1:26270944
|
G | A | 232 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1650-70G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270944 | ||||||
chr1:26271182
|
G | A | 187 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0298others(184): Show | 192 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1743+75G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26271182 | ||||||
chr1:26271290
|
C | T | 29 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0003t0004g0302others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1743+183C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26271290 | ||||||
chr1:26271505
|
G | A | 1 | a0001c0016t0011g0324 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1743+398G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26271505 | ||||||
chr1:26271550
|
A | G | 79 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0315others(76): Show | 81 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.1743+443A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26271550 | ||||||
chr1:26271568
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1744-453C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26271568 | ||||||
chr1:26271616
|
G | A | 1 | a0004c0004t0003g0296 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1744-405G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26271616 | ||||||
chr1:26271624
|
C | T | 1 | a0001c0016t0011g0324 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1744-397C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26271624 | ||||||
chr1:26271790
|
T | C | 97 | a0001c0001t0001g0315a0001c0001t0003g0003a0001c0001t0003g0092others(94): Show | 99 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1744-231T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26271790 | ||||||
chr1:26271877
|
A | T | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1744-144A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26271877 | ||||||
chr1:26272017
|
T | G | 2 | a0003c0005t0004g0322a0003c0005t0004g0323 | 2 | HG02622.hp2 HG02896.hp2 |
splice_region_variant&intron_variant | LOW | c.1744-4T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26272017 | ||||||
chr1:26272136
|
A | G | 1 | a0001c0001t0002g0035 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1794+65A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272136 | ||||||
chr1:26272360
|
G | T | 1 | a0002c0002t0001g0236 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1794+289G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272360 | ||||||
chr1:26272541
|
C | G | 1 | a0001c0001t0003g0118 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1794+470C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272541 | ||||||
chr1:26272586
|
C | G | 84 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0315others(81): Show | 86 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.1794+515C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272586 | ||||||
chr1:26272617
|
A | AT | 50 | a0001c0001t0001g0179a0001c0001t0001g0186a0001c0001t0001g0189others(47): Show | 50 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1794+573dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | |||||
chr1:26272617
|
A | ATT | 14 | a0001c0001t0002g0034a0001c0001t0003g0099a0001c0001t0003g0101others(11): Show | 14 | HG01071.hp2 HG01099.hp2 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.1794+572_1794+573d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | |||||
chr1:26272617
|
A | ATTT | 28 | a0001c0001t0003g0003a0001c0001t0003g0092a0001c0001t0003g0097others(25): Show | 30 | HG00639.hp2 HG00733.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1794+571_1794+573d others(5): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | |||||
chr1:26272617
|
A | ATTTT | 19 | a0001c0001t0001g0315a0001c0001t0002g0172a0001c0001t0003g0098others(16): Show | 19 | HG00323.hp2 HG00544.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1794+570_1794+573d others(6): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | |||||
chr1:26272617
|
A | ATTTTT | 6 | a0001c0001t0003g0114a0001c0001t0003g0119a0001c0001t0003g0126others(3): Show | 6 | HG01358.hp2 HG01952.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1794+569_1794+573d others(7): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | |||||
chr1:26272617
|
A | ATTTTTT | 11 | a0001c0001t0003g0104a0001c0001t0003g0127a0001c0001t0003g0128others(8): Show | 11 | HG02293.hp2 HG03516.hp1 NA18906.hp2 others(8): Show |
intron_variant | MODIFIER | c.1794+568_1794+573d others(8): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | |||||
chr1:26272617
|
A | ATTTTTTT others(3): Show |
1 | a0004c0004t0003g0296 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1794+564_1794+573d others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | |||||
chr1:26272617
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0284 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1794+562_1794+573d others(14): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | |||||
chr1:26272617
|
A | ATTTTTTT others(29): Show |
1 | a0001c0001t0001g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1794+573_1794+574i others(38): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | |||||
chr1:26272617
|
AT | A | 11 | a0001c0001t0001g0181a0001c0001t0001g0298a0001c0001t0001g0299others(8): Show | 11 | HG01167.hp2 HG01515.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1794+573delT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | |||||
chr1:26272641
|
T | G | 2 | a0003c0007t0004g0320a0003c0007t0004g0321 | 2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1794+570T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272641 | ||||||
chr1:26272642
|
T | G | 24 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0003t0004g0302others(21): Show | 24 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.1794+571T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272642 | ||||||
chr1:26272642
|
T | TG | 3 | a0003c0003t0004g0318a0003c0003t0006g0096a0010c0017t0004g0306 | 3 | HG01361.hp1 HG02572.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1794+571_1794+572i others(3): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272642 | ||||||
chr1:26272645
|
G | T | 27 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0003t0004g0302others(24): Show | 27 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.1794+574G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272645 | ||||||
chr1:26272668
|
G | A | 2 | a0003c0008t0004g0308a0003c0008t0004g0309 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1794+597G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272668 | ||||||
chr1:26272697
|
C | T | 29 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0003t0004g0302others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1794+626C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272697 | ||||||
chr1:26272769
|
C | T | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1794+698C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272769 | ||||||
chr1:26272778
|
A | G | 232 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1794+707A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272778 | ||||||
chr1:26272790
|
G | A | 1 | a0001c0001t0003g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1794+719G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272790 | ||||||
chr1:26272817
|
C | T | 1 | a0001c0001t0002g0080 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1794+746C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272817 | ||||||
chr1:26272881
|
G | A | 1 | a0003c0003t0004g0319 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1794+810G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272881 | ||||||
chr1:26272998
|
A | G | 72 | a0001c0001t0001g0315a0001c0001t0003g0003a0001c0001t0003g0092others(69): Show | 74 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1794+927A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272998 | ||||||
chr1:26273044
|
G | A | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG01167.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1794+973G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273044 | ||||||
chr1:26273051
|
G | A | 29 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0003t0004g0302others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1794+980G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273051 | ||||||
chr1:26273097
|
G | C | 1 | a0002c0002t0007g0213 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1794+1026G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273097 | ||||||
chr1:26273098
|
A | G | 1 | a0002c0002t0007g0213 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1794+1027A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273098 | ||||||
chr1:26273099
|
G | A | 1 | a0002c0002t0007g0213 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1794+1028G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273099 | ||||||
chr1:26273105
|
A | G | 2 | a0002c0002t0001g0271a0002c0002t0001g0276 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1794+1034A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273105 | ||||||
chr1:26273258
|
G | A | 3 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0003t0004g0313 | 3 | HG02896.hp1 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1794+1187G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273258 | ||||||
chr1:26273317
|
G | T | 1 | a0001c0001t0001g0183 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1794+1246G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273317 | ||||||
chr1:26273350
|
C | T | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1794+1279C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273350 | ||||||
chr1:26273724
|
G | A | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1795-1240G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273724 | ||||||
chr1:26273813
|
T | C | 232 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1795-1151T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273813 | ||||||
chr1:26273846
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1795-1118G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273846 | ||||||
chr1:26273900
|
C | CTAAA | 69 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(66): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.1795-1064_1795-106 others(8): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273900 | ||||||
chr1:26273900
|
C | CTAAATAA others(1): Show |
44 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(41): Show | 45 | HG00140.hp1 HG00609.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.1795-1064_1795-106 others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273900 | ||||||
chr1:26273900
|
C | CTAAATAA others(5): Show |
3 | a0001c0001t0001g0285a0005c0006t0001g0261a0005c0006t0001g0278 | 3 | HG01891.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1795-1064_1795-106 others(16): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273900 | ||||||
chr1:26273900
|
C | CTAAATAA others(9): Show |
1 | a0002c0002t0001g0225 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1795-1064_1795-106 others(20): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273900 | ||||||
chr1:26273901
|
A | AAAAT | 9 | a0001c0001t0002g0033a0001c0001t0002g0041a0004c0004t0003g0292others(6): Show | 9 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1795-1035_1795-103 others(8): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26273901 | |||||
chr1:26273901
|
A | AAAATAAA others(1): Show |
55 | a0001c0001t0003g0003a0001c0001t0003g0099a0001c0001t0003g0100others(52): Show | 57 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1795-1039_1795-103 others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26273901 | |||||
chr1:26273901
|
A | AAAATAAA others(5): Show |
11 | a0001c0001t0001g0315a0001c0001t0003g0098a0001c0001t0003g0136others(8): Show | 11 | HG01358.hp2 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1795-1043_1795-103 others(16): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26273901 | |||||
chr1:26273901
|
A | AAAATAAA others(9): Show |
1 | a0001c0001t0003g0155 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1795-1047_1795-103 others(20): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26273901 | |||||
chr1:26273901
|
A | T | 119 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(116): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.1795-1063A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273901 | ||||||
chr1:26273931
|
A | AATAAAT | 5 | a0003c0003t0004g0312a0003c0003t0004g0316a0003c0005t0004g0297others(2): Show | 5 | HG00741.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795-1032_1795-103 others(10): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26273931 | |||||
chr1:26273931
|
A | AATAAATA others(3): Show |
22 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0003t0004g0302others(19): Show | 22 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.1795-1032_1795-103 others(14): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26273931 | |||||
chr1:26273932
|
A | ATAAATAA others(3): Show |
5 | a0001c0001t0003g0092a0001c0001t0003g0120a0001c0001t0003g0124others(2): Show | 5 | NA18952.hp2 NA18970.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795-1032_1795-103 others(14): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273932 | ||||||
chr1:26273934
|
T | A | 30 | a0001c0001t0003g0097a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1795-1030T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273934 | ||||||
chr1:26273992
|
A | G | 29 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0003t0004g0302others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1795-972A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273992 | ||||||
chr1:26274023
|
GT | G | 227 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(224): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1795-930delT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26274023 | |||||
chr1:26274192
|
CACTT | C | 22 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0003t0004g0302others(19): Show | 22 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.1795-769_1795-766d others(6): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26274192 | |||||
chr1:26274200
|
C | T | 1 | a0002c0002t0001g0286 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1795-764C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26274200 | ||||||
chr1:26274250
|
A | AT | 3 | a0001c0001t0002g0070a0001c0001t0002g0072a0001c0001t0002g0073 | 3 | NA18986.hp2 NA19068.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1795-713dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26274250 | |||||
chr1:26274302
|
A | G | 114 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(111): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.1795-662A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26274302 | ||||||
chr1:26274667
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1795-297G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26274667 | ||||||
chr1:26274882
|
T | C | 4 | a0004c0004t0003g0292a0004c0004t0008g0293a0004c0004t0008g0294others(1): Show | 4 | HG00639.hp1 HG02257.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795-82T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26274882 | ||||||
chr1:26274892
|
C | T | 3 | a0001c0001t0003g0127a0001c0001t0003g0158a0001c0001t0003g0164 | 3 | NA18986.hp1 NA19012.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1795-72C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26274892 | ||||||
chr1:26274894
|
G | A | 119 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(116): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.1795-70G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26274894 | ||||||
chr1:26275079
|
A | G | 30 | a0001c0001t0002g0033a0003c0003t0004g0300a0003c0003t0004g0301others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
splice_region_variant&intron_variant | LOW | c.1902+8A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275079 | ||||||
chr1:26275186
|
A | G | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1902+115A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275186 | ||||||
chr1:26275264
|
A | G | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1902+193A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275264 | ||||||
chr1:26275283
|
G | GT | 73 | a0001c0001t0001g0214a0001c0001t0001g0315a0001c0001t0002g0039others(70): Show | 75 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.1902+228dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 26275283 | |||||
chr1:26275283
|
GT | G | 6 | a0001c0001t0001g0181a0001c0001t0002g0044a0001c0001t0002g0077others(3): Show | 6 | HG01515.hp2 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1902+228delT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 26275283 | |||||
chr1:26275404
|
C | CTG | 9 | a0001c0001t0001g0284a0001c0001t0001g0285a0004c0004t0003g0292others(6): Show | 9 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1902+337_1902+338d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 26275404 | |||||
chr1:26275467
|
G | A | 7 | a0004c0004t0003g0292a0004c0004t0003g0295a0004c0004t0003g0296others(4): Show | 7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1902+396G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275467 | ||||||
chr1:26275760
|
C | T | 119 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(116): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.1902+689C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275760 | ||||||
chr1:26275765
|
T | G | 29 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0003t0004g0302others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1902+694T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275765 | ||||||
chr1:26275805
|
C | G | 1 | a0002c0002t0001g0232 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1903-730C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275805 | ||||||
chr1:26275816
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1903-719G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275816 | ||||||
chr1:26275820
|
G | T | 1 | a0001c0001t0002g0039 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-715G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275820 | ||||||
chr1:26275821
|
G | A | 1 | a0001c0001t0002g0039 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-714G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275821 | ||||||
chr1:26275822
|
A | T | 1 | a0001c0001t0002g0039 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-713A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275822 | ||||||
chr1:26275823
|
C | A | 1 | a0001c0001t0002g0039 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-712C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275823 | ||||||
chr1:26275824
|
T | C | 1 | a0001c0001t0002g0039 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-711T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275824 | ||||||
chr1:26275825
|
C | A | 1 | a0001c0001t0002g0039 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-710C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275825 | ||||||
chr1:26275828
|
T | G | 1 | a0001c0001t0002g0039 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-707T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275828 | ||||||
chr1:26275830
|
C | G | 1 | a0001c0001t0002g0039 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-705C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275830 | ||||||
chr1:26275832
|
G | T | 1 | a0001c0001t0002g0039 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-703G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275832 | ||||||
chr1:26275833
|
A | G | 1 | a0001c0001t0002g0039 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-702A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275833 | ||||||
chr1:26275834
|
C | T | 1 | a0001c0001t0002g0039 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-701C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275834 | ||||||
chr1:26275867
|
G | A | 1 | a0003c0003t0004g0318 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1903-668G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275867 | ||||||
chr1:26276019
|
C | T | 2 | a0001c0001t0003g0150a0001c0001t0003g0156 | 2 | HG00544.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.1903-516C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26276019 | ||||||
chr1:26276023
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1903-512C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26276023 | ||||||
chr1:26276034
|
C | T | 29 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0003t0004g0302others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1903-501C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26276034 | ||||||
chr1:26276037
|
C | A | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1903-498C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26276037 | ||||||
chr1:26276059
|
T | C | 33 | a0001c0001t0001g0266a0001c0001t0001g0269a0002c0002t0001g0004others(30): Show | 34 | HG00621.hp2 HG01261.hp2 HG01975.hp1 others(31): Show |
intron_variant | MODIFIER | c.1903-476T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26276059 | ||||||
chr1:26276065
|
C | G | 41 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0178others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1903-470C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26276065 | ||||||
chr1:26276076
|
TGA | T | 29 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0003t0004g0302others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1903-458_1903-457d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26276076 | ||||||
chr1:26276328
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1903-207C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26276328 | ||||||
chr1:26276494
|
C | G | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1903-41C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26276494 | ||||||
chr1:26276800
|
CCTT | C | 5 | a0003c0003t0004g0302a0003c0003t0004g0310a0003c0003t0004g0311others(2): Show | 5 | HG00140.hp2 HG00323.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2128+44_2128+46del others(3): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 26276800 | |||||
chr1:26276957
|
C | A | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2129-179C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 13/13 | chr1 | 26276957 |