geneid | 9702 |
---|---|
ensemblid | ENSG00000166037.11 |
hgncid | 30794 |
symbol | CEP57 |
name | centrosomal protein 57 |
refseq_nuc | NM_014679.5 |
refseq_prot | NP_055494.2 |
ensembl_nuc | ENST00000325542.10 |
ensembl_prot | ENSP00000317902.5 |
mane_status | MANE Select |
chr | chr11 |
start | 95790498 |
end | 95832693 |
strand | + |
ver | v1.2 |
region | chr11:95790498-95832693 |
region5000 | chr11:95785498-95837693 |
regionname0 | CEP57_chr11_95790498_95832693 |
regionname5000 | CEP57_chr11_95785498_95837693 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 500 | 247 | 79 | 40 | 86 | 11 | 30 | 69 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0002 | 0/1 | 500 | 89 | 10 | 14 | 53 | 5 | 6 | 42 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0003 | 0/0 | 500 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0004 | 0/0 | 361 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0005 | 0/0 | 500 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0006 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1503 | 242 | 77 | 38 | 85 | 11 | 30 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
c0002 | 0/1 | 1503 | 87 | 10 | 13 | 52 | 5 | 6 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
c0003 | 0/0 | 1503 | 3 | 1 | 2 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
c0004 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
c0005 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
c0006 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
c0007 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
c0008 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
c0009 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
c0010 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
c0011 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 1639 | 127 | 12 | 26 | 64 | 10 | 14 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
t0002 | 0/0 | 1638 | 87 | 9 | 14 | 53 | 5 | 6 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
t0003 | 0/0 | 1639 | 61 | 38 | 11 | 8 | 1 | 3 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
t0004 | 0/0 | 1639 | 22 | 21 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
t0005 | 0/0 | 1639 | 21 | 3 | 3 | 14 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
t0006 | 0/0 | 1639 | 7 | 0 | 0 | 1 | 0 | 6 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
t0007 | 0/0 | 1639 | 6 | 0 | 1 | 0 | 0 | 5 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
t0008 | 0/0 | 1639 | 3 | 3 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
t0009 | 0/0 | 1639 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
t0010 | 0/1 | 1638 | 1 | 0 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
t0011 | 0/0 | 1639 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
t0012 | 0/0 | 1639 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
t0013 | 0/0 | 1639 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 18 | 10 | 3 | 3 | 1 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0002 | 0/0 | 9 | 0 | 2 | 5 | 0 | 2 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0004 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0015 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0016 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0021 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0022 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0045 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0052 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1503 | 242 | 77 | 38 | 85 | 11 | 30 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0001c0003 | 0/0 | 1503 | 3 | 1 | 2 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0001c0006 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0001c0011 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0002c0002 | 0/1 | 1503 | 87 | 10 | 13 | 52 | 5 | 6 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0002c0004 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0002c0007 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0003c0005 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0004c0009 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0005c0008 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0006c0010 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3141 | 124 | 12 | 25 | 62 | 10 | 14 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0001c0001t0003 | 0/0 | 3141 | 58 | 36 | 10 | 8 | 1 | 3 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0001c0001t0004 | 0/0 | 3141 | 21 | 20 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0001c0001t0005 | 0/0 | 3141 | 18 | 2 | 1 | 14 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0001c0001t0006 | 0/0 | 3141 | 7 | 0 | 0 | 1 | 0 | 6 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0001c0001t0007 | 0/0 | 3141 | 6 | 0 | 1 | 0 | 0 | 5 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0001c0001t0008 | 0/0 | 3141 | 3 | 3 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0001c0001t0009 | 0/0 | 3141 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0001c0001t0011 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0001c0001t0012 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0001c0001t0013 | 0/0 | 3141 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0001c0003t0005 | 0/0 | 3141 | 3 | 1 | 2 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0001c0006t0003 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0001c0011t0001 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0002c0002t0002 | 0/0 | 3140 | 85 | 9 | 13 | 52 | 5 | 6 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0002c0002t0004 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0002c0002t0010 | 0/1 | 3140 | 1 | 0 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0002c0004t0002 | 0/0 | 3140 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0002c0007t0002 | 0/0 | 3140 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0003c0005t0003 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0004c0009t0001 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0005c0008t0001 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
a0006c0010t0003 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | copy fasta | chr11 | 95785498 | 95837693 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 2 | 4 | 0 | 2 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0021 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0052 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0001 | 0/0 | 17 | 9 | 3 | 3 | 1 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0004g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0004g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0004g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0005g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0005g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0006g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0007g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0007g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0007g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0007g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0008g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0008g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0008g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0009g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0009g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0011g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0012g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0001t0013g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0003t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0003t0005g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0003t0005g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0006t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0001c0011t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0015 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0016 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0002t0010g0045 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0004t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0002c0007t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0003c0005t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0004c0009t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0005c0008t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
a0006c0010t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0032 | EUR | GBR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | FIN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0038 | EUR | FIN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | FIN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0197 | EUR | FIN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00544 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00597 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0207 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0219 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00639 | hp2 | a0002 | c0002 | t0002 | g0216 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0218 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01069 | hp2 | a0002 | c0002 | t0002 | g0221 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0195 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01081 | hp2 | a0001 | c0001 | t0005 | g0236 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01167 | hp1 | a0001 | c0003 | t0005 | g0251 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0033 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0162 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01169 | hp1 | a0001 | c0003 | t0005 | g0252 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01169 | hp2 | a0002 | c0002 | t0002 | g0033 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01175 | hp2 | a0002 | c0007 | t0002 | g0225 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0015 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0038 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0212 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01261 | hp2 | a0002 | c0002 | t0002 | g0183 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01361 | hp1 | a0003 | c0005 | t0003 | g0138 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0200 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0032 | EUR | IBS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01884 | hp1 | a0002 | c0002 | t0002 | g0016 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0158 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01891 | hp1 | a0002 | c0002 | t0002 | g0228 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0161 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01981 | hp2 | a0004 | c0009 | t0001 | g0088 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02056 | hp1 | a0001 | c0001 | t0005 | g0233 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0198 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0186 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02080 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02145 | hp2 | a0002 | c0002 | t0002 | g0220 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0224 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02280 | hp2 | a0001 | c0001 | t0008 | g0237 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02300 | hp2 | a0001 | c0001 | t0007 | g0129 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0234 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02622 | hp1 | a0001 | c0001 | t0009 | g0122 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02630 | hp2 | a0001 | c0001 | t0008 | g0238 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0239 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02647 | hp2 | a0001 | c0001 | t0012 | g0131 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0227 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0115 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02735 | hp1 | a0001 | c0001 | t0007 | g0025 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0217 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02738 | hp1 | a0001 | c0001 | t0013 | g0102 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0118 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02886 | hp2 | a0001 | c0006 | t0003 | g0148 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02895 | hp1 | a0002 | c0002 | t0002 | g0191 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02970 | hp1 | a0001 | c0001 | t0008 | g0235 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02976 | hp2 | a0002 | c0002 | t0002 | g0178 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03098 | hp1 | a0002 | c0002 | t0002 | g0034 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0041 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03139 | hp2 | a0006 | c0010 | t0003 | g0001 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03209 | hp1 | a0001 | c0001 | t0011 | g0135 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03209 | hp2 | a0002 | c0002 | t0002 | g0177 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03239 | hp1 | a0001 | c0001 | t0007 | g0127 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03239 | hp2 | a0001 | c0001 | t0006 | g0027 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03453 | hp1 | a0002 | c0002 | t0002 | g0223 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03491 | hp2 | a0001 | c0001 | t0006 | g0134 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0123 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0144 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0151 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03669 | hp1 | a0001 | c0001 | t0007 | g0049 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03688 | hp1 | a0001 | c0001 | t0006 | g0133 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0159 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0015 | SAS | BEB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0222 | SAS | BEB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03942 | hp1 | a0001 | c0001 | t0007 | g0025 | SAS | BEB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0181 | SAS | BEB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG04115 | hp1 | a0001 | c0001 | t0005 | g0241 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0152 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0044 | SAS | BEB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG04199 | hp1 | a0001 | c0001 | t0006 | g0137 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG04228 | hp1 | a0001 | c0001 | t0006 | g0132 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG04228 | hp2 | a0001 | c0001 | t0007 | g0130 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | YRI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | YRI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18747 | hp2 | a0002 | c0002 | t0002 | g0201 | EAS | CHB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18906 | hp1 | a0002 | c0002 | t0004 | g0232 | AFR | YRI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | YRI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18940 | hp1 | a0001 | c0001 | t0005 | g0246 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0206 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18945 | hp2 | a0001 | c0001 | t0005 | g0244 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18946 | hp2 | a0001 | c0001 | t0005 | g0247 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18947 | hp1 | a0001 | c0001 | t0005 | g0242 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18948 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18956 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18961 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18963 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18968 | hp1 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18969 | hp2 | a0001 | c0011 | t0001 | g0002 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18970 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18972 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18973 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18975 | hp2 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18979 | hp2 | a0001 | c0001 | t0005 | g0248 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18980 | hp1 | a0001 | c0001 | t0006 | g0027 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18982 | hp1 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18985 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18987 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18993 | hp2 | a0001 | c0001 | t0005 | g0243 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA18998 | hp2 | a0001 | c0001 | t0005 | g0249 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19000 | hp1 | a0001 | c0001 | t0005 | g0245 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19000 | hp2 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19001 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19007 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19009 | hp1 | a0005 | c0008 | t0001 | g0008 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19011 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | LWK | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | LWK | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0125 | AFR | LWK | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | LWK | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19063 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19072 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19074 | hp1 | a0002 | c0004 | t0002 | g0017 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19076 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19079 | hp2 | a0001 | c0001 | t0005 | g0240 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19082 | hp1 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19086 | hp1 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19091 | hp1 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0121 | AFR | YRI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | YRI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ASW | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA20129 | hp2 | a0001 | c0003 | t0005 | g0250 | AFR | ASW | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0192 | EUR | TSI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | TSI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | TSI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | TSI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA20905 | hp1 | a0001 | c0001 | t0006 | g0048 | SAS | GIH | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0116 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0117 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | USA | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | USA | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | USA | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0124 | AFR | USA | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0120 | AFR | LWK | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0226 | AFR | LWK | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0010 | g0045 | REF | REF | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0052 | REF | REF | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:95813062
|
G | C | 1 | a0003 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.333G>C | p.Gln111His | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 3/11 | 534/3141 | 333/1503 | 111/500 | chr11 | 95813062 | ||
chr11:95827879
|
A | G | 1 | a0006 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.979A>G | p.Ile327Val | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1180/3141 | 979/1503 | 327/500 | chr11 | 95827879 | ||
chr11:95827963
|
G | A | 1 | a0005 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.1063G>A | p.Gly355Ser | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1264/3141 | 1063/1503 | 355/500 | chr11 | 95827963 | ||
chr11:95827981
|
T | G | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1081T>G | p.Ser361Ala | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1282/3141 | 1081/1503 | 361/500 | chr11 | 95827981 | ||
chr11:95827982
|
C | A | 1 | a0004 | 1 | HG01981.hp2 | stop_gained | HIGH | c.1082C>A | p.Ser361* | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1283/3141 | 1082/1503 | 361/500 | chr11 | 95827982 | ||
chr11:95827984
|
G | T | 1 | a0004 | 1 | HG01981.hp2 | stop_gained | HIGH | c.1084G>T | p.Glu362* | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1285/3141 | 1084/1503 | 362/500 | chr11 | 95827984 | ||
chr11:95827987
|
G | C | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1087G>C | p.Val363Leu | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1288/3141 | 1087/1503 | 363/500 | chr11 | 95827987 | ||
chr11:95827991
|
T | C | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1091T>C | p.Leu364Ser | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1292/3141 | 1091/1503 | 364/500 | chr11 | 95827991 | ||
chr11:95827992
|
A | C | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1092A>C | p.Leu364Phe | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1293/3141 | 1092/1503 | 364/500 | chr11 | 95827992 | ||
chr11:95827994
|
A | T | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1094A>T | p.Gln365Leu | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1295/3141 | 1094/1503 | 365/500 | chr11 | 95827994 | ||
chr11:95828000
|
T | G | 1 | a0004 | 1 | HG01981.hp2 | stop_gained | HIGH | c.1100T>G | p.Leu367* | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1301/3141 | 1100/1503 | 367/500 | chr11 | 95828000 | ||
chr11:95828003
|
A | T | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1103A>T | p.Gln368Leu | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1304/3141 | 1103/1503 | 368/500 | chr11 | 95828003 | ||
chr11:95828004
|
G | C | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1104G>C | p.Gln368His | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1305/3141 | 1104/1503 | 368/500 | chr11 | 95828004 | ||
chr11:95828008
|
G | C | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1108G>C | p.Glu370Gln | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1309/3141 | 1108/1503 | 370/500 | chr11 | 95828008 | ||
chr11:95828015
|
G | C | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1115G>C | p.Gly372Ala | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1316/3141 | 1115/1503 | 372/500 | chr11 | 95828015 | ||
chr11:95828023
|
A | C | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1123A>C | p.Ser375Arg | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1324/3141 | 1123/1503 | 375/500 | chr11 | 95828023 | ||
chr11:95828024
|
G | T | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1124G>T | p.Ser375Ile | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1325/3141 | 1124/1503 | 375/500 | chr11 | 95828024 | ||
chr11:95831095
|
A | G | 1 | a0002 | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
missense_variant | MODERATE | c.1342A>G | p.Arg448Gly | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 11/11 | 1543/3141 | 1342/1503 | 448/500 | chr11 | 95831095 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:95799309
|
G | A | 1 | a0002c0004 | 1 | NA19074.hp1 | synonymous_variant | LOW | c.123G>A | p.Ser41Ser | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/11 | 324/3141 | 123/1503 | 41/500 | chr11 | 95799309 | ||
chr11:95818838
|
A | G | 1 | a0001c0011 | 1 | NA18969.hp2 | synonymous_variant | LOW | c.633A>G | p.Gln211Gln | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/11 | 834/3141 | 633/1503 | 211/500 | chr11 | 95818838 | ||
chr11:95821924
|
G | A | 2 | a0001c0006a0002c0007 | 2 | HG01175.hp2 HG02886.hp2 |
synonymous_variant | LOW | c.753G>A | p.Pro251Pro | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 7/11 | 954/3141 | 753/1503 | 251/500 | chr11 | 95821924 | ||
chr11:95821969
|
A | G | 1 | a0001c0003 | 3 | HG01167.hp1 HG01169.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.798A>G | p.Pro266Pro | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 7/11 | 999/3141 | 798/1503 | 266/500 | chr11 | 95821969 | ||
chr11:95828016
|
G | A | 1 | a0004c0009 | 1 | HG01981.hp2 | synonymous_variant | LOW | c.1116G>A | p.Gly372Gly | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1317/3141 | 1116/1503 | 372/500 | chr11 | 95828016 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:95790498
|
C | T | 1 | a0001c0001t0008 | 3 | HG02280.hp2 HG02630.hp2 HG02970.hp1 |
5_prime_UTR_variant | MODIFIER | c.-201C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/11 | 201 | chr11 | 95790498 | |||||
chr11:95790577
|
G | A | 2 | a0001c0001t0006a0002c0002t0010 | 8 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-122G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/11 | 122 | chr11 | 95790577 | |||||
chr11:95790646
|
A | G | 3 | a0001c0001t0005a0001c0001t0008a0001c0003t0005 | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-53A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/11 | 53 | chr11 | 95790646 | |||||
chr11:95790671
|
T | C | 1 | a0001c0001t0007 | 6 | HG02300.hp2 HG02735.hp1 HG03239.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-28T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/11 | 28 | chr11 | 95790671 | |||||
chr11:95790684
|
T | G | 1 | a0001c0001t0011 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-15T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/11 | 15 | chr11 | 95790684 | |||||
chr11:95831628
|
A | T | 1 | a0001c0001t0013 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*372A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 11/11 | 372 | chr11 | 95831628 | |||||
chr11:95832047
|
A | G | 1 | a0001c0001t0009 | 2 | HG02622.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*791A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 11/11 | 791 | chr11 | 95832047 | |||||
chr11:95832124
|
A | G | 14 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(11): Show | 197 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*868A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 11/11 | 868 | chr11 | 95832124 | |||||
chr11:95832444
|
TA | T | 4 | a0002c0002t0002a0002c0002t0010a0002c0004t0002others(1): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1190delA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 11/11 | 1190 | INFO_REALIGN_3_PRIME | chr11 | 95832444 | ||||
chr11:95832617
|
C | A | 1 | a0001c0001t0012 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1361C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 11/11 | 1361 | chr11 | 95832617 | |||||
chr11:95832625
|
G | A | 4 | a0002c0002t0002a0002c0002t0010a0002c0004t0002others(1): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1369G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 11/11 | 1369 | chr11 | 95832625 | |||||
chr11:95832676
|
G | A | 4 | a0001c0001t0003a0001c0006t0003a0003c0005t0003others(1): Show | 61 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1420G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 11/11 | 1420 | chr11 | 95832676 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:95790808
|
G | A | 1 | a0001c0001t0004g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.45+65G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95790808 | ||||||
chr11:95790818
|
G | A | 2 | a0002c0002t0002g0042a0002c0002t0002g0043 | 2 | HG00438.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.45+75G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95790818 | ||||||
chr11:95790863
|
G | A | 1 | a0002c0002t0002g0044 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.45+120G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95790863 | ||||||
chr11:95790903
|
G | T | 97 | a0001c0001t0001g0173a0001c0001t0005g0039a0001c0001t0005g0040others(94): Show | 113 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.45+160G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95790903 | ||||||
chr11:95790969
|
C | T | 24 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0005g0039others(21): Show | 26 | HG01081.hp2 HG01109.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.45+226C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95790969 | ||||||
chr11:95791221
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.45+478C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95791221 | ||||||
chr11:95791257
|
G | A | 98 | a0001c0001t0001g0173a0001c0001t0005g0039a0001c0001t0005g0040others(95): Show | 114 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.45+514G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95791257 | ||||||
chr11:95791432
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.45+689C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95791432 | ||||||
chr11:95791549
|
A | G | 7 | a0001c0001t0001g0031a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 8 | HG00609.hp2 HG00621.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+806A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95791549 | ||||||
chr11:95791555
|
C | T | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.45+812C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95791555 | ||||||
chr11:95791681
|
A | T | 1 | a0002c0002t0004g0232 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.45+938A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95791681 | ||||||
chr11:95791694
|
G | T | 33 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0007others(30): Show | 61 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.45+951G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95791694 | ||||||
chr11:95792228
|
GC | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0046a0001c0001t0001g0047 | 4 | HG01515.hp1 HG01517.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+1486delC | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792228 | ||||||
chr11:95792284
|
C | A | 1 | a0001c0001t0006g0048 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.45+1541C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792284 | ||||||
chr11:95792502
|
G | A | 1 | a0001c0001t0007g0049 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.45+1759G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792502 | ||||||
chr11:95792639
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.45+1896T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792639 | ||||||
chr11:95792689
|
C | G | 1 | a0001c0001t0006g0137 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.45+1946C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792689 | ||||||
chr11:95792708
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.45+1965A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792708 | ||||||
chr11:95792757
|
G | A | 1 | a0001c0001t0005g0233 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.45+2014G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792757 | ||||||
chr11:95792759
|
A | T | 3 | a0001c0003t0005g0250a0001c0003t0005g0251a0001c0003t0005g0252 | 3 | HG01167.hp1 HG01169.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.45+2016A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792759 | ||||||
chr11:95792792
|
T | C | 1 | a0003c0005t0003g0138 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.45+2049T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792792 | ||||||
chr11:95792922
|
T | TA | 94 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(91): Show | 110 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.45+2192dupA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 95792922 | |||||
chr11:95792953
|
A | G | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.45+2210A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792953 | ||||||
chr11:95793083
|
A | C | 1 | a0001c0001t0004g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.45+2340A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95793083 | ||||||
chr11:95793234
|
T | A | 1 | a0001c0001t0004g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.45+2491T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95793234 | ||||||
chr11:95793416
|
T | TTA | 235 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(232): Show | 316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.45+2673_45+2674ins others(2): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95793416 | ||||||
chr11:95793424
|
C | T | 5 | a0002c0002t0002g0224a0002c0002t0002g0226a0002c0002t0002g0227others(2): Show | 5 | HG01175.hp2 HG01891.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+2681C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95793424 | ||||||
chr11:95793551
|
C | CTT | 165 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(162): Show | 221 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.45+2809_45+2810ins others(2): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 95793551 | |||||
chr11:95793731
|
G | C | 1 | a0002c0002t0002g0174 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.45+2988G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95793731 | ||||||
chr11:95793761
|
A | C | 1 | a0001c0001t0001g0112 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.45+3018A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95793761 | ||||||
chr11:95793788
|
A | G | 1 | a0001c0001t0001g0068 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.45+3045A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95793788 | ||||||
chr11:95793795
|
T | C | 1 | a0001c0001t0003g0139 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.45+3052T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95793795 | ||||||
chr11:95793822
|
G | T | 1 | a0001c0001t0001g0068 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.45+3079G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95793822 | ||||||
chr11:95794046
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.45+3303A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95794046 | ||||||
chr11:95794097
|
G | A | 1 | a0001c0001t0007g0049 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.45+3354G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95794097 | ||||||
chr11:95794213
|
T | C | 3 | a0001c0001t0003g0007a0001c0001t0003g0140a0001c0001t0003g0141 | 6 | HG00738.hp2 HG00741.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+3470T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95794213 | ||||||
chr11:95794329
|
A | G | 1 | a0001c0001t0011g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.45+3586A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95794329 | ||||||
chr11:95794361
|
T | G | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.45+3618T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95794361 | ||||||
chr11:95794487
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+3744G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95794487 | ||||||
chr11:95794569
|
A | AGT | 3 | a0001c0001t0004g0114a0002c0002t0002g0175a0002c0002t0002g0176 | 3 | HG02040.hp2 HG02055.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.45+3841_45+3842dup others(2): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 95794569 | |||||
chr11:95794763
|
A | G | 1 | a0003c0005t0003g0138 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.45+4020A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95794763 | ||||||
chr11:95794881
|
G | A | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.45+4138G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95794881 | ||||||
chr11:95794980
|
G | T | 2 | a0001c0003t0005g0251a0001c0003t0005g0252 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.45+4237G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95794980 | ||||||
chr11:95795043
|
G | A | 1 | a0002c0002t0002g0175 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.46-4189G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795043 | ||||||
chr11:95795045
|
G | A | 73 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(70): Show | 87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.46-4187G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795045 | ||||||
chr11:95795060
|
C | T | 6 | a0001c0001t0006g0027a0001c0001t0006g0048a0001c0001t0006g0132others(3): Show | 7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-4172C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795060 | ||||||
chr11:95795346
|
T | A | 1 | a0001c0001t0003g0142 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.46-3886T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795346 | ||||||
chr11:95795369
|
ACT | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0108a0001c0001t0001g0109others(2): Show | 7 | HG00423.hp1 NA18940.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-3860_46-3859del others(2): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 95795369 | |||||
chr11:95795462
|
T | C | 13 | a0001c0001t0004g0006a0001c0001t0004g0012a0001c0001t0004g0023others(10): Show | 19 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.46-3770T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795462 | ||||||
chr11:95795484
|
T | G | 1 | a0001c0001t0001g0069 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.46-3748T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795484 | ||||||
chr11:95795499
|
C | CT | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.46-3722dupT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 95795499 | |||||
chr11:95795499
|
C | CTT | 6 | a0002c0002t0002g0038a0002c0002t0002g0219a0002c0002t0002g0220others(3): Show | 7 | HG00280.hp2 HG00639.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-3723_46-3722dup others(2): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 95795499 | |||||
chr11:95795550
|
C | T | 97 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(94): Show | 113 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.46-3682C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795550 | ||||||
chr11:95795578
|
C | T | 1 | a0001c0001t0004g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.46-3654C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795578 | ||||||
chr11:95795727
|
G | T | 20 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0028others(17): Show | 43 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.46-3505G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795727 | ||||||
chr11:95795842
|
CAT | C | 16 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(13): Show | 18 | HG01167.hp1 HG01169.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.46-3389_46-3388del others(2): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795842 | ||||||
chr11:95795858
|
C | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.46-3374C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795858 | ||||||
chr11:95795900
|
A | C | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.46-3332A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795900 | ||||||
chr11:95796048
|
C | G | 1 | a0001c0001t0001g0168 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.46-3184C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95796048 | ||||||
chr11:95796078
|
T | G | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.46-3154T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95796078 | ||||||
chr11:95796237
|
T | C | 1 | a0001c0001t0001g0024 | 2 | HG03490.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.46-2995T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95796237 | ||||||
chr11:95796427
|
C | T | 16 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0069others(13): Show | 18 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(15): Show |
intron_variant | MODIFIER | c.46-2805C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95796427 | ||||||
chr11:95796961
|
C | G | 73 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(70): Show | 87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.46-2271C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95796961 | ||||||
chr11:95796990
|
A | G | 1 | a0001c0001t0001g0026 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.46-2242A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95796990 | ||||||
chr11:95797101
|
C | T | 11 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(8): Show | 16 | HG02300.hp2 HG02630.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.46-2131C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797101 | ||||||
chr11:95797130
|
C | T | 1 | a0002c0002t0002g0218 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.46-2102C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797130 | ||||||
chr11:95797189
|
C | T | 1 | a0001c0001t0005g0249 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.46-2043C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797189 | ||||||
chr11:95797200
|
T | A | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.46-2032T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797200 | ||||||
chr11:95797272
|
T | G | 1 | a0001c0001t0003g0143 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.46-1960T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797272 | ||||||
chr11:95797365
|
A | T | 2 | a0002c0002t0002g0217a0002c0002t0002g0218 | 2 | HG00741.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.46-1867A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797365 | ||||||
chr11:95797703
|
A | G | 46 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0007others(43): Show | 80 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.46-1529A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797703 | ||||||
chr11:95797723
|
T | C | 7 | a0001c0001t0001g0008a0001c0001t0001g0053a0001c0001t0001g0054others(4): Show | 8 | HG00544.hp1 HG00621.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.46-1509T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797723 | ||||||
chr11:95797745
|
A | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.46-1487A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797745 | ||||||
chr11:95797901
|
A | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.46-1331A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797901 | ||||||
chr11:95798487
|
A | G | 1 | a0001c0001t0005g0249 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.46-745A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95798487 | ||||||
chr11:95798555
|
A | C | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.46-677A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95798555 | ||||||
chr11:95798584
|
G | A | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.46-648G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95798584 | ||||||
chr11:95799002
|
A | G | 74 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(71): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.46-230A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95799002 | ||||||
chr11:95799631
|
A | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202+243A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95799631 | ||||||
chr11:95799676
|
A | G | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.202+288A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95799676 | ||||||
chr11:95799753
|
A | G | 1 | a0002c0002t0002g0216 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.202+365A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95799753 | ||||||
chr11:95800028
|
G | A | 1 | a0002c0002t0004g0232 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.202+640G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95800028 | ||||||
chr11:95800038
|
C | T | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202+650C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95800038 | ||||||
chr11:95800136
|
G | C | 1 | a0001c0001t0001g0070 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.202+748G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95800136 | ||||||
chr11:95800383
|
C | CT | 10 | a0001c0001t0003g0007a0001c0001t0003g0140a0001c0001t0003g0141others(7): Show | 14 | HG00738.hp2 HG00741.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.202+1007dupT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95800383 | |||||
chr11:95800393
|
T | A | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.202+1005T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95800393 | ||||||
chr11:95800402
|
T | C | 1 | a0001c0003t0005g0250 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.202+1014T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95800402 | ||||||
chr11:95800463
|
C | T | 164 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(161): Show | 220 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.202+1075C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95800463 | ||||||
chr11:95800500
|
A | G | 3 | a0002c0002t0002g0213a0002c0002t0002g0214a0002c0002t0002g0215 | 3 | NA18969.hp1 NA19063.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.202+1112A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95800500 | ||||||
chr11:95800748
|
G | A | 6 | a0001c0001t0006g0027a0001c0001t0006g0048a0001c0001t0006g0132others(3): Show | 7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.202+1360G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95800748 | ||||||
chr11:95800763
|
GGTTAT | G | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.202+1381_202+1385d others(7): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95800763 | |||||
chr11:95800992
|
T | C | 3 | a0001c0001t0001g0051a0001c0001t0001g0058a0001c0001t0001g0059 | 3 | HG01167.hp2 HG01192.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.202+1604T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95800992 | ||||||
chr11:95801012
|
A | G | 11 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(8): Show | 16 | HG02300.hp2 HG02630.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.202+1624A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801012 | ||||||
chr11:95801080
|
G | T | 16 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0069others(13): Show | 18 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(15): Show |
intron_variant | MODIFIER | c.202+1692G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801080 | ||||||
chr11:95801248
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.202+1860G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801248 | ||||||
chr11:95801276
|
T | G | 2 | a0002c0002t0002g0177a0002c0002t0002g0178 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.202+1888T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801276 | ||||||
chr11:95801277
|
G | A | 165 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(162): Show | 221 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.202+1889G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801277 | ||||||
chr11:95801289
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.202+1901C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801289 | ||||||
chr11:95801297
|
C | T | 3 | a0001c0001t0005g0247a0001c0001t0005g0248a0001c0001t0005g0249 | 3 | NA18946.hp2 NA18979.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.202+1909C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801297 | ||||||
chr11:95801316
|
G | A | 1 | a0001c0001t0003g0140 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.202+1928G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801316 | ||||||
chr11:95801324
|
A | T | 1 | a0002c0002t0002g0212 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.202+1936A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801324 | ||||||
chr11:95801450
|
C | CA | 50 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0108others(47): Show | 62 | HG00423.hp2 HG00738.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.202+2081dupA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95801450 | |||||
chr11:95801450
|
C | CAA | 7 | a0001c0001t0005g0240a0001c0001t0006g0027a0001c0001t0006g0048others(4): Show | 8 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.202+2080_202+2081d others(4): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95801450 | |||||
chr11:95801450
|
CA | C | 8 | a0001c0001t0001g0021a0001c0001t0001g0101a0001c0001t0001g0107others(5): Show | 9 | HG01257.hp1 HG02257.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.202+2081delA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95801450 | |||||
chr11:95801495
|
A | C | 1 | a0001c0001t0005g0239 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.202+2107A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801495 | ||||||
chr11:95801763
|
G | A | 3 | a0002c0002t0002g0032a0002c0002t0002g0212a0002c0002t0002g0216 | 4 | HG00099.hp1 HG00639.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+2375G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801763 | ||||||
chr11:95801829
|
A | C | 1 | a0001c0001t0006g0134 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.202+2441A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801829 | ||||||
chr11:95801924
|
A | C | 3 | a0001c0001t0003g0143a0001c0001t0003g0150a0001c0001t0003g0151 | 3 | HG02922.hp2 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.202+2536A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801924 | ||||||
chr11:95802154
|
C | T | 1 | a0001c0001t0003g0028 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.202+2766C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95802154 | ||||||
chr11:95802251
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG00642.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.202+2863C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95802251 | ||||||
chr11:95802255
|
A | AT | 7 | a0001c0001t0001g0100a0001c0001t0001g0110a0001c0001t0004g0123others(4): Show | 7 | HG00423.hp1 HG01891.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.202+2886dupT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95802255 | |||||
chr11:95802255
|
AT | A | 13 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0003g0155others(10): Show | 14 | HG02976.hp1 HG03239.hp2 HG03453.hp1 others(11): Show |
intron_variant | MODIFIER | c.202+2886delT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95802255 | |||||
chr11:95802255
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0004g0124 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.202+2876_202+2886d others(13): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95802255 | |||||
chr11:95802346
|
C | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG00642.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.202+2958C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95802346 | ||||||
chr11:95802390
|
G | T | 1 | a0001c0001t0001g0073 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.202+3002G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95802390 | ||||||
chr11:95802886
|
A | C | 2 | a0001c0001t0004g0124a0001c0001t0004g0126 | 2 | HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.202+3498A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95802886 | ||||||
chr11:95802918
|
C | T | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.202+3530C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95802918 | ||||||
chr11:95802993
|
C | A | 3 | a0001c0001t0003g0029a0001c0001t0003g0156a0001c0001t0003g0157 | 4 | HG02818.hp1 HG02922.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+3605C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95802993 | ||||||
chr11:95803047
|
A | T | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 4 | HG02080.hp2 NA18950.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+3659A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803047 | ||||||
chr11:95803410
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0013g0102 | 2 | HG00280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.202+4022T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803410 | ||||||
chr11:95803500
|
G | T | 1 | a0001c0001t0003g0162 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.202+4112G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803500 | ||||||
chr11:95803519
|
A | G | 1 | a0001c0001t0012g0131 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.202+4131A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803519 | ||||||
chr11:95803530
|
A | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202+4142A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803530 | ||||||
chr11:95803560
|
T | C | 98 | a0001c0001t0004g0041a0001c0001t0005g0039a0001c0001t0005g0040others(95): Show | 114 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.202+4172T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803560 | ||||||
chr11:95803561
|
G | GC | 25 | a0001c0001t0001g0108a0001c0001t0005g0234a0001c0001t0005g0241others(22): Show | 28 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.202+4180dupC | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95803561 | |||||
chr11:95803568
|
C | T | 1 | a0001c0001t0003g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.202+4180C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803568 | ||||||
chr11:95803569
|
G | T | 1 | a0001c0001t0007g0130 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.202+4181G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803569 | ||||||
chr11:95803628
|
C | A | 1 | a0002c0002t0002g0189 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.202+4240C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803628 | ||||||
chr11:95803706
|
G | A | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.202+4318G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803706 | ||||||
chr11:95803745
|
C | CT | 59 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(56): Show | 71 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.202+4366dupT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95803745 | |||||
chr11:95803745
|
C | CTT | 16 | a0002c0002t0002g0018a0002c0002t0002g0185a0002c0002t0002g0186others(13): Show | 18 | HG00609.hp1 HG02071.hp1 HG03453.hp1 others(15): Show |
intron_variant | MODIFIER | c.202+4365_202+4366d others(4): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95803745 | |||||
chr11:95803751
|
T | A | 1 | a0001c0003t0005g0250 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.202+4363T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803751 | ||||||
chr11:95804194
|
G | A | 97 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(94): Show | 113 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.202+4806G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95804194 | ||||||
chr11:95804352
|
G | A | 3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0168 | 3 | HG00621.hp2 NA19001.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.202+4964G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95804352 | ||||||
chr11:95804422
|
C | T | 6 | a0001c0001t0006g0027a0001c0001t0006g0048a0001c0001t0006g0132others(3): Show | 7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.202+5034C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95804422 | ||||||
chr11:95804538
|
C | T | 1 | a0001c0001t0004g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.202+5150C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95804538 | ||||||
chr11:95804575
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.202+5187G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95804575 | ||||||
chr11:95804598
|
T | G | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.202+5210T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95804598 | ||||||
chr11:95804664
|
C | T | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.202+5276C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95804664 | ||||||
chr11:95804721
|
TATAA | T | 7 | a0002c0002t0002g0017a0002c0002t0002g0035a0002c0002t0002g0174others(4): Show | 9 | NA18945.hp1 NA18946.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+5336_202+5339d others(6): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95804721 | |||||
chr11:95804867
|
A | AT | 13 | a0001c0001t0004g0006a0001c0001t0004g0012a0001c0001t0004g0023others(10): Show | 19 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.202+5486dupT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95804867 | |||||
chr11:95805106
|
G | A | 97 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(94): Show | 113 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.202+5718G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805106 | ||||||
chr11:95805373
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.202+5985C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805373 | ||||||
chr11:95805378
|
T | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202+5990T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805378 | ||||||
chr11:95805440
|
A | C | 11 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(8): Show | 16 | HG02300.hp2 HG02630.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.202+6052A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805440 | ||||||
chr11:95805459
|
C | T | 61 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(58): Show | 100 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.202+6071C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805459 | ||||||
chr11:95805460
|
G | A | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.202+6072G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805460 | ||||||
chr11:95805593
|
C | A | 1 | a0002c0002t0002g0229 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.202+6205C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805593 | ||||||
chr11:95805614
|
G | A | 61 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(58): Show | 100 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.202+6226G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805614 | ||||||
chr11:95805855
|
T | G | 1 | a0002c0002t0002g0224 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.202+6467T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805855 | ||||||
chr11:95805958
|
T | A | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.202+6570T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805958 | ||||||
chr11:95806033
|
A | T | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.202+6645A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806033 | ||||||
chr11:95806110
|
A | G | 1 | a0001c0001t0011g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.202+6722A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806110 | ||||||
chr11:95806256
|
G | A | 1 | a0002c0002t0002g0044 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.203-6676G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806256 | ||||||
chr11:95806353
|
G | A | 1 | a0001c0001t0005g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.203-6579G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806353 | ||||||
chr11:95806354
|
G | C | 1 | a0001c0001t0004g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.203-6578G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806354 | ||||||
chr11:95806400
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0101 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.203-6532G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806400 | ||||||
chr11:95806427
|
G | T | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.203-6505G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806427 | ||||||
chr11:95806442
|
C | T | 13 | a0001c0001t0004g0006a0001c0001t0004g0012a0001c0001t0004g0023others(10): Show | 19 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.203-6490C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806442 | ||||||
chr11:95806443
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.203-6489G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806443 | ||||||
chr11:95806450
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.203-6482G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806450 | ||||||
chr11:95806590
|
TG | T | 11 | a0001c0001t0003g0007a0001c0001t0003g0014a0001c0001t0003g0140others(8): Show | 16 | HG00738.hp2 HG00741.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.203-6341delG | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806590 | ||||||
chr11:95806611
|
G | C | 2 | a0002c0002t0002g0219a0002c0002t0002g0221 | 2 | HG00639.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.203-6321G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806611 | ||||||
chr11:95806728
|
A | G | 165 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(162): Show | 221 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.203-6204A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806728 | ||||||
chr11:95806815
|
C | A | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.203-6117C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806815 | ||||||
chr11:95806876
|
T | C | 165 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(162): Show | 221 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.203-6056T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806876 | ||||||
chr11:95806905
|
C | G | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-6027C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806905 | ||||||
chr11:95806905
|
C | T | 13 | a0001c0001t0004g0006a0001c0001t0004g0012a0001c0001t0004g0023others(10): Show | 19 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.203-6027C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806905 | ||||||
chr11:95806998
|
C | T | 1 | a0001c0001t0004g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.203-5934C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806998 | ||||||
chr11:95807153
|
G | T | 3 | a0001c0001t0005g0040a0001c0001t0005g0242a0001c0001t0005g0243 | 4 | NA18947.hp1 NA18963.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-5779G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807153 | ||||||
chr11:95807206
|
A | T | 1 | a0001c0001t0003g0140 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.203-5726A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807206 | ||||||
chr11:95807212
|
A | C | 1 | a0001c0001t0005g0239 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.203-5720A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807212 | ||||||
chr11:95807246
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.203-5686G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807246 | ||||||
chr11:95807401
|
C | T | 61 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(58): Show | 100 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.203-5531C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807401 | ||||||
chr11:95807483
|
C | T | 1 | a0002c0002t0002g0044 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.203-5449C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807483 | ||||||
chr11:95807507
|
C | T | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-5425C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807507 | ||||||
chr11:95807539
|
T | C | 1 | a0001c0001t0005g0241 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.203-5393T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807539 | ||||||
chr11:95807703
|
G | C | 1 | a0001c0001t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.203-5229G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807703 | ||||||
chr11:95807763
|
G | A | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-5169G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807763 | ||||||
chr11:95807771
|
T | C | 1 | a0001c0001t0001g0019 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.203-5161T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807771 | ||||||
chr11:95808009
|
A | C | 1 | a0002c0002t0002g0210 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.203-4923A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808009 | ||||||
chr11:95808091
|
C | T | 36 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0007others(33): Show | 64 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.203-4841C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808091 | ||||||
chr11:95808123
|
T | C | 164 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(161): Show | 220 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.203-4809T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808123 | ||||||
chr11:95808308
|
A | T | 13 | a0001c0001t0004g0006a0001c0001t0004g0012a0001c0001t0004g0023others(10): Show | 19 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.203-4624A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808308 | ||||||
chr11:95808344
|
T | C | 71 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(68): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.203-4588T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808344 | ||||||
chr11:95808490
|
G | C | 1 | a0001c0001t0004g0126 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.203-4442G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808490 | ||||||
chr11:95808585
|
A | G | 61 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(58): Show | 100 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.203-4347A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808585 | ||||||
chr11:95808783
|
T | C | 1 | a0002c0002t0002g0185 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.203-4149T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808783 | ||||||
chr11:95808850
|
G | A | 1 | a0002c0002t0004g0232 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.203-4082G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808850 | ||||||
chr11:95808866
|
T | C | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-4066T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808866 | ||||||
chr11:95808932
|
A | G | 1 | a0001c0001t0004g0012 | 3 | HG02109.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.203-4000A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808932 | ||||||
chr11:95809154
|
C | T | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.203-3778C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809154 | ||||||
chr11:95809208
|
T | C | 1 | a0001c0001t0005g0247 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.203-3724T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809208 | ||||||
chr11:95809245
|
A | G | 11 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(8): Show | 16 | HG02300.hp2 HG02630.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.203-3687A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809245 | ||||||
chr11:95809382
|
A | G | 6 | a0001c0001t0006g0027a0001c0001t0006g0048a0001c0001t0006g0132others(3): Show | 7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-3550A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809382 | ||||||
chr11:95809577
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0171a0001c0001t0001g0172 | 5 | HG00642.hp1 HG01109.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.203-3355C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809577 | ||||||
chr11:95809581
|
A | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.203-3351A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809581 | ||||||
chr11:95809684
|
G | C | 1 | a0001c0001t0003g0158 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.203-3248G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809684 | ||||||
chr11:95809692
|
A | T | 1 | a0001c0001t0004g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.203-3240A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809692 | ||||||
chr11:95809718
|
A | T | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-3214A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809718 | ||||||
chr11:95809776
|
G | T | 1 | a0001c0001t0004g0123 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.203-3156G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809776 | ||||||
chr11:95810046
|
G | A | 4 | a0002c0002t0002g0186a0002c0002t0002g0187a0002c0002t0002g0189others(1): Show | 4 | HG02071.hp1 NA18942.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-2886G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810046 | ||||||
chr11:95810047
|
T | A | 74 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(71): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.203-2885T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810047 | ||||||
chr11:95810355
|
A | G | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-2577A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810355 | ||||||
chr11:95810427
|
T | A | 1 | a0002c0002t0002g0222 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.203-2505T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810427 | ||||||
chr11:95810456
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.203-2476C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810456 | ||||||
chr11:95810457
|
G | A | 13 | a0001c0001t0004g0006a0001c0001t0004g0012a0001c0001t0004g0023others(10): Show | 19 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.203-2475G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810457 | ||||||
chr11:95810470
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.203-2462A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810470 | ||||||
chr11:95810546
|
A | T | 1 | a0001c0001t0001g0093 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.203-2386A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810546 | ||||||
chr11:95810551
|
C | G | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.203-2381C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810551 | ||||||
chr11:95810752
|
C | T | 1 | a0001c0001t0005g0239 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.203-2180C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810752 | ||||||
chr11:95810816
|
C | A | 164 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(161): Show | 220 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.203-2116C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810816 | ||||||
chr11:95810825
|
G | A | 1 | a0001c0001t0003g0145 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.203-2107G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810825 | ||||||
chr11:95810851
|
A | G | 1 | a0002c0002t0002g0042 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.203-2081A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810851 | ||||||
chr11:95811028
|
G | A | 6 | a0001c0001t0006g0027a0001c0001t0006g0048a0001c0001t0006g0132others(3): Show | 7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-1904G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811028 | ||||||
chr11:95811118
|
A | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | NA18939.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.203-1814A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811118 | ||||||
chr11:95811149
|
G | A | 1 | a0002c0002t0002g0190 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.203-1783G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811149 | ||||||
chr11:95811153
|
C | T | 3 | a0001c0001t0008g0235a0001c0001t0008g0237a0001c0001t0008g0238 | 3 | HG02280.hp2 HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.203-1779C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811153 | ||||||
chr11:95811154
|
G | T | 3 | a0001c0001t0008g0235a0001c0001t0008g0237a0001c0001t0008g0238 | 3 | HG02280.hp2 HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.203-1778G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811154 | ||||||
chr11:95811155
|
G | A | 3 | a0001c0001t0008g0235a0001c0001t0008g0237a0001c0001t0008g0238 | 3 | HG02280.hp2 HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.203-1777G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811155 | ||||||
chr11:95811204
|
G | C | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-1728G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811204 | ||||||
chr11:95811227
|
A | G | 74 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(71): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.203-1705A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811227 | ||||||
chr11:95811252
|
A | G | 3 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126 | 3 | HG03041.hp2 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.203-1680A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811252 | ||||||
chr11:95811428
|
C | T | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.203-1504C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811428 | ||||||
chr11:95811437
|
G | C | 8 | a0002c0002t0002g0038a0002c0002t0002g0217a0002c0002t0002g0218others(5): Show | 9 | HG00280.hp2 HG00639.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.203-1495G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811437 | ||||||
chr11:95811442
|
A | G | 1 | a0001c0001t0001g0057 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.203-1490A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811442 | ||||||
chr11:95811442
|
A | T | 1 | a0001c0001t0006g0048 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.203-1490A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811442 | ||||||
chr11:95811444
|
G | C | 1 | a0001c0001t0007g0130 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.203-1488G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811444 | ||||||
chr11:95811517
|
C | T | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.203-1415C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811517 | ||||||
chr11:95811522
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.203-1410A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811522 | ||||||
chr11:95811580
|
T | TA | 6 | a0001c0001t0001g0058a0001c0001t0005g0245a0001c0001t0005g0249others(3): Show | 6 | HG01175.hp2 HG01192.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.203-1338dupA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95811580 | |||||
chr11:95811580
|
TA | T | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0003g0014others(4): Show | 9 | HG02258.hp1 HG02451.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.203-1338delA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95811580 | |||||
chr11:95811595
|
C | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0094 | 2 | HG00738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.203-1337C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811595 | ||||||
chr11:95811596
|
G | A | 1 | a0002c0002t0002g0215 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.203-1336G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811596 | ||||||
chr11:95811605
|
A | G | 4 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(1): Show | 4 | HG00621.hp1 NA18939.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.203-1327A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811605 | ||||||
chr11:95811619
|
C | A | 1 | a0001c0001t0004g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.203-1313C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811619 | ||||||
chr11:95811650
|
A | G | 11 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(8): Show | 16 | HG02300.hp2 HG02630.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.203-1282A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811650 | ||||||
chr11:95811741
|
C | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.203-1191C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811741 | ||||||
chr11:95811741
|
C | T | 1 | a0002c0002t0002g0215 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.203-1191C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811741 | ||||||
chr11:95811944
|
CAT | C | 164 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(161): Show | 220 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.203-985_203-984del others(2): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95811944 | |||||
chr11:95811949
|
T | G | 164 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(161): Show | 220 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.203-983T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811949 | ||||||
chr11:95812002
|
T | C | 1 | a0001c0001t0011g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.203-930T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812002 | ||||||
chr11:95812006
|
A | G | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.203-926A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812006 | ||||||
chr11:95812020
|
G | A | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.203-912G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812020 | ||||||
chr11:95812069
|
A | G | 1 | a0001c0001t0005g0239 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.203-863A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812069 | ||||||
chr11:95812160
|
T | C | 1 | a0001c0001t0004g0114 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.203-772T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812160 | ||||||
chr11:95812176
|
T | G | 13 | a0001c0001t0004g0006a0001c0001t0004g0012a0001c0001t0004g0023others(10): Show | 19 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.203-756T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812176 | ||||||
chr11:95812205
|
T | C | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.203-727T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812205 | ||||||
chr11:95812423
|
T | A | 74 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(71): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.203-509T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812423 | ||||||
chr11:95812587
|
C | T | 1 | a0001c0001t0003g0028 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.203-345C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812587 | ||||||
chr11:95812791
|
C | A | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-141C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812791 | ||||||
chr11:95812792
|
A | C | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-140A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812792 | ||||||
chr11:95813177
|
A | G | 74 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(71): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.382+66A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 3/10 | chr11 | 95813177 | ||||||
chr11:95813628
|
T | C | 3 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126 | 3 | HG03041.hp2 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.504+39T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95813628 | ||||||
chr11:95813763
|
T | C | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.504+174T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95813763 | ||||||
chr11:95813778
|
A | G | 2 | a0001c0001t0009g0118a0001c0001t0009g0122 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.504+189A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95813778 | ||||||
chr11:95813852
|
A | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.504+263A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95813852 | ||||||
chr11:95813857
|
G | T | 1 | a0002c0002t0002g0203 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.504+268G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95813857 | ||||||
chr11:95813922
|
G | A | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.504+333G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95813922 | ||||||
chr11:95814069
|
ATCT | A | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.504+481_504+483del others(3): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814069 | ||||||
chr11:95814073
|
C | A | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.504+484C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814073 | ||||||
chr11:95814075
|
C | T | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.504+486C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814075 | ||||||
chr11:95814076
|
T | A | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.504+487T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814076 | ||||||
chr11:95814077
|
C | G | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.504+488C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814077 | ||||||
chr11:95814078
|
T | G | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.504+489T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814078 | ||||||
chr11:95814166
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.504+577C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814166 | ||||||
chr11:95814197
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.504+608C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814197 | ||||||
chr11:95814206
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0009g0118 | 2 | HG02886.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.504+617C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814206 | ||||||
chr11:95814306
|
C | T | 7 | a0001c0001t0001g0031a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 8 | HG00609.hp2 HG00621.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.504+717C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814306 | ||||||
chr11:95814324
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.504+735C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814324 | ||||||
chr11:95814357
|
A | AT | 12 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0067others(9): Show | 12 | HG00621.hp2 HG02071.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.504+788dupT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 95814357 | |||||
chr11:95814357
|
A | ATTTT | 15 | a0001c0001t0005g0040a0001c0001t0005g0233a0001c0001t0005g0234others(12): Show | 16 | HG01081.hp2 HG01167.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.504+785_504+788dup others(4): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 95814357 | |||||
chr11:95814357
|
AT | A | 12 | a0001c0001t0001g0056a0001c0001t0001g0061a0001c0001t0001g0079others(9): Show | 13 | HG02698.hp2 HG02818.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.504+788delT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 95814357 | |||||
chr11:95814403
|
C | T | 74 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(71): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.504+814C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814403 | ||||||
chr11:95814422
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.504+833G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814422 | ||||||
chr11:95814441
|
A | G | 1 | a0002c0002t0002g0218 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.504+852A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814441 | ||||||
chr11:95814546
|
G | C | 1 | a0001c0001t0007g0127 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.504+957G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814546 | ||||||
chr11:95814651
|
C | T | 1 | a0001c0001t0007g0129 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.504+1062C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814651 | ||||||
chr11:95814670
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.504+1081A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814670 | ||||||
chr11:95814763
|
T | A | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.504+1174T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814763 | ||||||
chr11:95814970
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.504+1381T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814970 | ||||||
chr11:95814985
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.504+1396C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814985 | ||||||
chr11:95815136
|
G | A | 3 | a0002c0002t0002g0032a0002c0002t0002g0212a0002c0002t0002g0216 | 4 | HG00099.hp1 HG00639.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+1547G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95815136 | ||||||
chr11:95815164
|
C | T | 6 | a0001c0001t0006g0027a0001c0001t0006g0048a0001c0001t0006g0132others(3): Show | 7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.504+1575C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95815164 | ||||||
chr11:95815195
|
A | G | 74 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(71): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.504+1606A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95815195 | ||||||
chr11:95815404
|
C | T | 50 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0007others(47): Show | 84 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.504+1815C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95815404 | ||||||
chr11:95815426
|
T | C | 9 | a0001c0001t0004g0023a0001c0001t0004g0114a0001c0001t0004g0115others(6): Show | 10 | HG02055.hp2 HG02257.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.504+1837T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95815426 | ||||||
chr11:95815509
|
CT | C | 71 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(68): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.504+1929delT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 95815509 | |||||
chr11:95816503
|
T | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG02148.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.505-1284T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95816503 | ||||||
chr11:95816613
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.505-1174C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95816613 | ||||||
chr11:95816784
|
G | A | 2 | a0002c0002t0002g0033a0002c0002t0002g0192 | 3 | HG01168.hp1 HG01169.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.505-1003G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95816784 | ||||||
chr11:95816823
|
C | T | 74 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(71): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.505-964C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95816823 | ||||||
chr11:95816923
|
A | G | 6 | a0001c0001t0006g0027a0001c0001t0006g0048a0001c0001t0006g0132others(3): Show | 7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.505-864A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95816923 | ||||||
chr11:95817150
|
G | A | 6 | a0001c0001t0006g0027a0001c0001t0006g0048a0001c0001t0006g0132others(3): Show | 7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.505-637G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95817150 | ||||||
chr11:95817308
|
G | A | 164 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(161): Show | 220 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.505-479G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95817308 | ||||||
chr11:95817331
|
A | G | 1 | a0001c0001t0005g0233 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.505-456A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95817331 | ||||||
chr11:95817646
|
C | G | 36 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(33): Show | 64 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.505-141C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95817646 | ||||||
chr11:95817677
|
C | T | 60 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(57): Show | 99 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.505-110C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95817677 | ||||||
chr11:95817972
|
C | T | 97 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(94): Show | 113 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.621+69C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 5/10 | chr11 | 95817972 | ||||||
chr11:95817988
|
T | C | 1 | a0002c0002t0002g0182 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.621+85T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 5/10 | chr11 | 95817988 | ||||||
chr11:95818123
|
T | A | 1 | a0001c0001t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.621+220T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 5/10 | chr11 | 95818123 | ||||||
chr11:95818133
|
C | T | 1 | a0002c0002t0002g0201 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.621+230C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 5/10 | chr11 | 95818133 | ||||||
chr11:95818276
|
G | A | 1 | a0001c0001t0009g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.621+373G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 5/10 | chr11 | 95818276 | ||||||
chr11:95818411
|
C | CA | 72 | a0001c0001t0001g0065a0002c0002t0002g0015a0002c0002t0002g0016others(69): Show | 86 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.622-401dupA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr11 | 95818411 | |||||
chr11:95818430
|
A | C | 6 | a0001c0001t0006g0027a0001c0001t0006g0048a0001c0001t0006g0132others(3): Show | 7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.622-397A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 5/10 | chr11 | 95818430 | ||||||
chr11:95818508
|
A | G | 1 | a0001c0001t0005g0236 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.622-319A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 5/10 | chr11 | 95818508 | ||||||
chr11:95818562
|
T | A | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.622-265T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 5/10 | chr11 | 95818562 | ||||||
chr11:95818948
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.699+44G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95818948 | ||||||
chr11:95818981
|
G | T | 1 | a0001c0001t0003g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.699+77G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95818981 | ||||||
chr11:95819001
|
T | G | 3 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126 | 3 | HG03041.hp2 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.699+97T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95819001 | ||||||
chr11:95819145
|
C | A | 3 | a0002c0002t0002g0036a0002c0002t0002g0190a0002c0002t0002g0211 | 4 | NA18968.hp1 NA18970.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.699+241C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95819145 | ||||||
chr11:95819596
|
A | C | 1 | a0001c0001t0006g0133 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.699+692A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95819596 | ||||||
chr11:95819739
|
C | T | 22 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(19): Show | 24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.699+835C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95819739 | ||||||
chr11:95819872
|
C | G | 3 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126 | 3 | HG03041.hp2 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.699+968C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95819872 | ||||||
chr11:95819904
|
T | TTTG | 97 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(94): Show | 113 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.699+1009_699+1011d others(5): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 95819904 | |||||
chr11:95820351
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.699+1447G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95820351 | ||||||
chr11:95820360
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.699+1456T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95820360 | ||||||
chr11:95820367
|
CTGAGGTC others(7): Show |
C | 2 | a0001c0001t0003g0030a0001c0001t0003g0142 | 3 | NA18943.hp1 NA19054.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.699+1482_700-1472d others(16): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 95820367 | |||||
chr11:95820464
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.700-1407G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95820464 | ||||||
chr11:95820538
|
T | A | 2 | a0002c0002t0002g0193a0002c0002t0002g0199 | 2 | NA18954.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.700-1333T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95820538 | ||||||
chr11:95820579
|
C | CA | 31 | a0001c0001t0001g0062a0001c0001t0001g0085a0001c0001t0001g0096others(28): Show | 33 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.700-1274dupA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 95820579 | |||||
chr11:95820579
|
C | CAAAA | 56 | a0002c0002t0002g0016a0002c0002t0002g0017a0002c0002t0002g0018others(53): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.700-1277_700-1274d others(6): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 95820579 | |||||
chr11:95820579
|
C | CAAAAA | 17 | a0002c0002t0002g0015a0002c0002t0002g0033a0002c0002t0002g0042others(14): Show | 20 | HG00438.hp1 HG01071.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.700-1278_700-1274d others(7): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 95820579 | |||||
chr11:95820726
|
G | T | 6 | a0001c0001t0006g0027a0001c0001t0006g0048a0001c0001t0006g0132others(3): Show | 7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.700-1145G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95820726 | ||||||
chr11:95820802
|
T | C | 2 | a0002c0002t0002g0184a0002c0002t0002g0196 | 2 | HG02135.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.700-1069T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95820802 | ||||||
chr11:95821006
|
A | G | 6 | a0001c0001t0006g0027a0001c0001t0006g0048a0001c0001t0006g0132others(3): Show | 7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.700-865A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95821006 | ||||||
chr11:95821119
|
G | A | 97 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(94): Show | 113 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.700-752G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95821119 | ||||||
chr11:95821147
|
A | G | 71 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(68): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.700-724A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95821147 | ||||||
chr11:95821427
|
A | G | 1 | a0001c0001t0011g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.700-444A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95821427 | ||||||
chr11:95821752
|
A | G | 1 | a0001c0001t0005g0239 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.700-119A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95821752 | ||||||
chr11:95821777
|
A | G | 1 | a0002c0002t0002g0208 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.700-94A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95821777 | ||||||
chr11:95821986
|
G | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099 | 3 | NA18950.hp1 NA18970.hp2 NA19062.hp1 |
splice_region_variant&intron_variant | LOW | c.807+8G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 7/10 | chr11 | 95821986 | ||||||
chr11:95822380
|
A | C | 1 | a0002c0002t0002g0201 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.808-119A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 7/10 | chr11 | 95822380 | ||||||
chr11:95822677
|
G | GTGCCTTT others(16): Show |
75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.885+102_885+124dup others(23): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95822677 | |||||
chr11:95823017
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0128 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.885+441C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823017 | ||||||
chr11:95823018
|
G | A | 33 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0007others(30): Show | 61 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.885+442G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823018 | ||||||
chr11:95823093
|
G | A | 25 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126others(22): Show | 27 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.885+517G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823093 | ||||||
chr11:95823139
|
G | T | 1 | a0002c0002t0002g0195 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.885+563G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823139 | ||||||
chr11:95823400
|
T | C | 3 | a0001c0001t0008g0235a0001c0001t0008g0237a0001c0001t0008g0238 | 3 | HG02280.hp2 HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.885+824T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823400 | ||||||
chr11:95823532
|
C | T | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.885+956C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823532 | ||||||
chr11:95823552
|
GT | G | 20 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(17): Show | 26 | HG00323.hp2 HG02300.hp2 HG02630.hp1 others(23): Show |
intron_variant | MODIFIER | c.885+984delT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95823552 | |||||
chr11:95823570
|
T | G | 1 | a0002c0002t0004g0232 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.885+994T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823570 | ||||||
chr11:95823592
|
GACT | G | 6 | a0001c0001t0003g0005a0001c0001t0003g0014a0001c0001t0003g0144others(3): Show | 12 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.885+1019_885+1021d others(5): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95823592 | |||||
chr11:95823630
|
CAG | C | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.885+1058_885+1059d others(4): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95823630 | |||||
chr11:95823691
|
C | T | 1 | a0001c0001t0011g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.885+1115C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823691 | ||||||
chr11:95823784
|
T | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.885+1208T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823784 | ||||||
chr11:95823838
|
C | A | 1 | a0001c0001t0003g0156 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.885+1262C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823838 | ||||||
chr11:95823865
|
G | GTTTA | 3 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126 | 3 | HG03041.hp2 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.885+1290_885+1293d others(6): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95823865 | |||||
chr11:95824070
|
T | C | 1 | a0002c0002t0002g0207 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.885+1494T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95824070 | ||||||
chr11:95824073
|
T | TA | 22 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(19): Show | 27 | HG02055.hp1 HG02135.hp1 HG02559.hp1 others(24): Show |
intron_variant | MODIFIER | c.885+1520dupA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95824073 | |||||
chr11:95824073
|
TA | T | 88 | a0001c0001t0001g0069a0001c0001t0001g0112a0001c0001t0003g0161others(85): Show | 102 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.885+1520delA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95824073 | |||||
chr11:95824073
|
TAA | T | 8 | a0001c0001t0005g0241a0001c0003t0005g0252a0002c0002t0002g0032others(5): Show | 9 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.885+1519_885+1520d others(4): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95824073 | |||||
chr11:95824258
|
T | A | 6 | a0001c0001t0006g0027a0001c0001t0006g0048a0001c0001t0006g0132others(3): Show | 7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.885+1682T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95824258 | ||||||
chr11:95824259
|
A | T | 49 | a0001c0001t0001g0063a0001c0001t0003g0001a0001c0001t0003g0005others(46): Show | 83 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.885+1683A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95824259 | ||||||
chr11:95824260
|
A | T | 4 | a0001c0001t0004g0023a0001c0001t0004g0041a0001c0001t0004g0115others(1): Show | 5 | HG02257.hp2 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.885+1684A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95824260 | ||||||
chr11:95824351
|
G | A | 5 | a0001c0001t0005g0039a0001c0001t0005g0240a0001c0001t0005g0244others(2): Show | 6 | NA18940.hp1 NA18945.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.885+1775G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95824351 | ||||||
chr11:95824406
|
ACT | A | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.885+1833_885+1834d others(4): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95824406 | |||||
chr11:95824552
|
G | A | 1 | a0002c0002t0004g0232 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.885+1976G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95824552 | ||||||
chr11:95824874
|
C | G | 1 | a0002c0002t0002g0205 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.885+2298C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95824874 | ||||||
chr11:95824983
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.885+2407C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95824983 | ||||||
chr11:95825100
|
C | T | 2 | a0001c0001t0003g0153a0001c0001t0003g0160 | 2 | HG00423.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.885+2524C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95825100 | ||||||
chr11:95825254
|
T | A | 25 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126others(22): Show | 27 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.886-2532T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95825254 | ||||||
chr11:95825395
|
C | T | 6 | a0001c0001t0006g0027a0001c0001t0006g0048a0001c0001t0006g0132others(3): Show | 7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.886-2391C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95825395 | ||||||
chr11:95825411
|
G | A | 1 | a0001c0001t0006g0133 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.886-2375G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95825411 | ||||||
chr11:95825454
|
A | G | 13 | a0001c0001t0004g0006a0001c0001t0004g0012a0001c0001t0004g0023others(10): Show | 19 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.886-2332A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95825454 | ||||||
chr11:95825593
|
C | CT | 18 | a0001c0001t0001g0057a0001c0001t0001g0063a0001c0001t0001g0077others(15): Show | 20 | HG01175.hp2 HG02055.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.886-2172dupT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95825593 | |||||
chr11:95825593
|
C | CTT | 6 | a0001c0001t0006g0027a0001c0001t0006g0048a0001c0001t0006g0132others(3): Show | 7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.886-2173_886-2172d others(4): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95825593 | |||||
chr11:95825593
|
CT | C | 20 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(17): Show | 25 | HG00438.hp1 HG01168.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.886-2172delT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95825593 | |||||
chr11:95825611
|
T | A | 11 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(8): Show | 16 | HG02300.hp2 HG02630.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.886-2175T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95825611 | ||||||
chr11:95825631
|
C | G | 1 | a0002c0002t0002g0212 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.886-2155C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95825631 | ||||||
chr11:95825782
|
A | C | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.886-2004A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95825782 | ||||||
chr11:95825789
|
G | T | 1 | a0002c0002t0002g0229 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.886-1997G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95825789 | ||||||
chr11:95825871
|
TCTGTAAT others(4): Show |
T | 1 | a0001c0001t0011g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.886-1903_886-1893d others(13): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95825871 | |||||
chr11:95826033
|
G | A | 1 | a0002c0002t0002g0218 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.886-1753G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826033 | ||||||
chr11:95826074
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0083 | 3 | HG01496.hp2 HG02559.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.886-1712A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826074 | ||||||
chr11:95826105
|
T | C | 1 | a0001c0001t0003g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.886-1681T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826105 | ||||||
chr11:95826106
|
T | A | 1 | a0001c0001t0003g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.886-1680T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826106 | ||||||
chr11:95826165
|
C | T | 6 | a0001c0001t0006g0027a0001c0001t0006g0048a0001c0001t0006g0132others(3): Show | 7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.886-1621C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826165 | ||||||
chr11:95826223
|
T | C | 1 | a0001c0001t0005g0244 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.886-1563T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826223 | ||||||
chr11:95826353
|
T | C | 74 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(71): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.886-1433T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826353 | ||||||
chr11:95826600
|
GA | G | 47 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0007others(44): Show | 81 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.886-1177delA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95826600 | |||||
chr11:95826645
|
C | T | 1 | a0001c0001t0003g0151 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.886-1141C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826645 | ||||||
chr11:95826677
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.886-1109C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826677 | ||||||
chr11:95826745
|
T | C | 11 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(8): Show | 16 | HG02300.hp2 HG02630.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.886-1041T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826745 | ||||||
chr11:95826825
|
T | C | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | NA18939.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.886-961T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826825 | ||||||
chr11:95826930
|
A | G | 4 | a0001c0001t0003g0014a0001c0001t0003g0144a0001c0001t0003g0145others(1): Show | 6 | HG02258.hp1 HG02451.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.886-856A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826930 | ||||||
chr11:95827083
|
T | G | 1 | a0001c0001t0003g0143 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.886-703T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827083 | ||||||
chr11:95827207
|
G | A | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.886-579G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827207 | ||||||
chr11:95827221
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.886-565A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827221 | ||||||
chr11:95827284
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.886-502C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827284 | ||||||
chr11:95827309
|
T | C | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.886-477T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827309 | ||||||
chr11:95827375
|
T | G | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.886-411T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827375 | ||||||
chr11:95827531
|
A | G | 50 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0007others(47): Show | 84 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.886-255A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827531 | ||||||
chr11:95827590
|
TTTTCCAT others(6): Show |
T | 13 | a0001c0001t0004g0006a0001c0001t0004g0012a0001c0001t0004g0023others(10): Show | 19 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.886-195_886-183del others(13): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827590 | ||||||
chr11:95827684
|
A | C | 1 | a0001c0001t0004g0116 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.886-102A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827684 | ||||||
chr11:95827689
|
A | G | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.886-97A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827689 | ||||||
chr11:95828028
|
G | C | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | splice_donor_variant&intron_variant | HIGH | c.1127+1G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828028 | ||||||
chr11:95828041
|
T | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+14T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828041 | ||||||
chr11:95828042
|
T | C | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+15T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828042 | ||||||
chr11:95828046
|
T | C | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+19T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828046 | ||||||
chr11:95828047
|
T | A | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+20T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828047 | ||||||
chr11:95828049
|
T | A | 1 | a0001c0001t0001g0013 | 3 | HG02818.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1127+22T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828049 | ||||||
chr11:95828051
|
A | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+24A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828051 | ||||||
chr11:95828054
|
T | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+27T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828054 | ||||||
chr11:95828058
|
T | A | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+31T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828058 | ||||||
chr11:95828059
|
T | C | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+32T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828059 | ||||||
chr11:95828064
|
T | TCGAAACA others(4): Show |
1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+38_1127+39ins others(11): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 95828064 | |||||
chr11:95828069
|
A | C | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+42A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828069 | ||||||
chr11:95828072
|
C | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+45C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828072 | ||||||
chr11:95828073
|
T | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+46T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828073 | ||||||
chr11:95828077
|
T | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+50T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828077 | ||||||
chr11:95828078
|
T | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+51T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828078 | ||||||
chr11:95828079
|
T | C | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+52T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828079 | ||||||
chr11:95828085
|
A | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+58A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828085 | ||||||
chr11:95828086
|
A | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+59A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828086 | ||||||
chr11:95828092
|
T | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+65T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828092 | ||||||
chr11:95828101
|
TA | T | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1127+77delA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 95828101 | |||||
chr11:95828130
|
A | G | 25 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126others(22): Show | 27 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.1127+103A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828130 | ||||||
chr11:95828149
|
A | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+122A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828149 | ||||||
chr11:95828324
|
T | G | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1127+297T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828324 | ||||||
chr11:95828480
|
C | CAT | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1127+454_1127+455d others(4): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 95828480 | |||||
chr11:95828505
|
A | G | 1 | a0002c0002t0002g0210 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1127+478A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828505 | ||||||
chr11:95828518
|
G | A | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1127+491G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828518 | ||||||
chr11:95828553
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1127+526A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828553 | ||||||
chr11:95828577
|
C | T | 97 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0233others(94): Show | 113 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.1127+550C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828577 | ||||||
chr11:95828709
|
C | T | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1128-478C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828709 | ||||||
chr11:95828801
|
A | G | 1 | a0001c0001t0004g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1128-386A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828801 | ||||||
chr11:95828959
|
G | A | 1 | a0001c0001t0001g0024 | 2 | HG03490.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1128-228G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828959 | ||||||
chr11:95829041
|
C | CA | 16 | a0001c0001t0001g0172a0001c0001t0004g0006a0001c0001t0004g0012others(13): Show | 22 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1128-130dupA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 95829041 | |||||
chr11:95829107
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1128-80G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95829107 | ||||||
chr11:95829163
|
G | A | 74 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(71): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1128-24G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95829163 | ||||||
chr11:95829371
|
G | GA | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1272+50dupA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 95829371 | |||||
chr11:95829381
|
A | C | 1 | a0001c0001t0011g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1272+50A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95829381 | ||||||
chr11:95829607
|
T | C | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1272+276T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95829607 | ||||||
chr11:95829666
|
TAA | T | 3 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126 | 3 | HG03041.hp2 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1272+336_1272+337d others(4): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95829666 | ||||||
chr11:95829704
|
C | G | 74 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(71): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1272+373C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95829704 | ||||||
chr11:95829835
|
A | G | 22 | a0001c0001t0003g0001a0001c0001t0003g0028a0001c0001t0003g0029others(19): Show | 41 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.1272+504A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95829835 | ||||||
chr11:95830064
|
T | G | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1272+733T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95830064 | ||||||
chr11:95830202
|
A | C | 2 | a0001c0001t0003g0150a0001c0001t0003g0151 | 2 | HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1273-824A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95830202 | ||||||
chr11:95830318
|
T | C | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1273-708T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95830318 | ||||||
chr11:95830342
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1273-684A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95830342 | ||||||
chr11:95830434
|
C | T | 1 | a0001c0001t0004g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1273-592C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95830434 | ||||||
chr11:95830566
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0046 | 6 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1273-460C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95830566 | ||||||
chr11:95830581
|
T | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0080others(1): Show | 9 | NA18942.hp2 NA18956.hp2 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.1273-445T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95830581 | ||||||
chr11:95830611
|
A | G | 75 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(72): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1273-415A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95830611 | ||||||
chr11:95830885
|
T | C | 1 | a0001c0001t0007g0049 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1273-141T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95830885 | ||||||
chr11:95830910
|
T | TTGAG | 155 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0026others(152): Show | 202 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.1273-115_1273-114i others(6): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 95830910 |