geneid | 22897 |
---|---|
ensemblid | ENSG00000110274.16 |
hgncid | 29182 |
symbol | CEP164 |
name | centrosomal protein 164 |
refseq_nuc | NM_014956.5 |
refseq_prot | NP_055771.4 |
ensembl_nuc | ENST00000278935.8 |
ensembl_prot | ENSP00000278935.3 |
mane_status | MANE Select |
chr | chr11 |
start | 117327854 |
end | 117413266 |
strand | + |
ver | v1.2 |
region | chr11:117327854-117413266 |
region5000 | chr11:117322854-117418266 |
regionname0 | CEP164_chr11_117327854_117413266 |
regionname5000 | CEP164_chr11_117322854_117418266 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1460 | 133 | 15 | 27 | 66 | 5 | 18 | 50 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0002 | 0/0 | 1460 | 102 | 21 | 11 | 60 | 4 | 6 | 43 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0003 | 0/0 | 1460 | 62 | 19 | 14 | 18 | 3 | 8 | 15 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0004 | 0/0 | 1460 | 53 | 15 | 10 | 17 | 3 | 8 | 16 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0005 | 0/0 | 1460 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0006 | 0/0 | 1460 | 6 | 0 | 0 | 5 | 0 | 1 | 4 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0007 | 0/0 | 1460 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0008 | 0/0 | 1460 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0009 | 0/0 | 1460 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0010 | 0/0 | 1460 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0011 | 0/0 | 1460 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0012 | 0/0 | 1460 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0013 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0014 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0015 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0016 | 0/0 | 1460 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0017 | 0/0 | 1460 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0018 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0019 | 0/0 | 1460 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0020 | 0/0 | 1460 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0021 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0022 | 0/0 | 1460 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0023 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0024 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0025 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0026 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 4383 | 101 | 21 | 11 | 59 | 4 | 6 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0002 | 0/0 | 4383 | 93 | 12 | 21 | 47 | 4 | 9 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0003 | 0/0 | 4383 | 61 | 18 | 14 | 18 | 3 | 8 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0004 | 0/0 | 4383 | 39 | 12 | 7 | 17 | 0 | 3 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0005 | 1/1 | 4383 | 35 | 2 | 6 | 15 | 1 | 9 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0006 | 0/0 | 4383 | 6 | 6 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0007 | 0/0 | 4383 | 6 | 0 | 0 | 5 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0008 | 0/0 | 4383 | 6 | 0 | 2 | 0 | 0 | 4 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0009 | 0/0 | 4383 | 4 | 1 | 0 | 0 | 2 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0010 | 0/0 | 4383 | 4 | 0 | 3 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0011 | 0/0 | 4383 | 3 | 3 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0012 | 0/0 | 4383 | 2 | 0 | 0 | 0 | 0 | 2 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0013 | 0/0 | 4383 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0014 | 0/0 | 4383 | 2 | 2 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0015 | 0/0 | 4383 | 2 | 0 | 1 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0016 | 0/0 | 4383 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0017 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0018 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0019 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0020 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0021 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0022 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0023 | 0/0 | 4383 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0024 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0025 | 0/0 | 4383 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0026 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0027 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0028 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0029 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0030 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0031 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0032 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0033 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0034 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0035 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0036 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0037 | 0/0 | 4383 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0038 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
c0039 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1247 | 81 | 24 | 17 | 27 | 4 | 9 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0002 | 0/0 | 1247 | 78 | 5 | 18 | 43 | 4 | 8 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0003 | 0/0 | 1247 | 73 | 14 | 6 | 46 | 2 | 5 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0004 | 0/0 | 1247 | 57 | 13 | 14 | 20 | 2 | 8 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0005 | 1/1 | 1247 | 50 | 9 | 8 | 22 | 1 | 8 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0006 | 0/0 | 1247 | 9 | 0 | 0 | 5 | 0 | 4 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0007 | 0/0 | 1247 | 7 | 7 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0008 | 0/0 | 1247 | 5 | 2 | 0 | 0 | 2 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0009 | 0/0 | 1247 | 5 | 3 | 2 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0010 | 0/0 | 1247 | 3 | 0 | 0 | 3 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0011 | 0/0 | 1248 | 3 | 0 | 0 | 1 | 1 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0012 | 0/0 | 1247 | 3 | 3 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0013 | 0/0 | 1247 | 3 | 3 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0014 | 0/0 | 1248 | 2 | 2 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0015 | 0/0 | 1247 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0016 | 0/0 | 1247 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0017 | 0/0 | 1247 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0018 | 0/0 | 1247 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0019 | 0/0 | 1247 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0020 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0021 | 0/0 | 1247 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0022 | 0/0 | 1247 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0023 | 0/0 | 1247 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0024 | 0/0 | 1247 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
t0025 | 0/0 | 1247 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0004 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0068 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0272 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 4383 | 93 | 12 | 21 | 47 | 4 | 9 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0001c0005 | 1/1 | 4383 | 35 | 2 | 6 | 15 | 1 | 9 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0001c0013 | 0/0 | 4383 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0001c0026 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0001c0027 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0001c0036 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0002c0001 | 0/0 | 4383 | 101 | 21 | 11 | 59 | 4 | 6 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0002c0038 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0003c0003 | 0/0 | 4383 | 61 | 18 | 14 | 18 | 3 | 8 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0003c0022 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0004c0004 | 0/0 | 4383 | 39 | 12 | 7 | 17 | 0 | 3 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0004c0008 | 0/0 | 4383 | 6 | 0 | 2 | 0 | 0 | 4 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0004c0009 | 0/0 | 4383 | 4 | 1 | 0 | 0 | 2 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0004c0015 | 0/0 | 4383 | 2 | 0 | 1 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0004c0031 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0004c0034 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0005c0006 | 0/0 | 4383 | 6 | 6 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0006c0007 | 0/0 | 4383 | 6 | 0 | 0 | 5 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0007c0010 | 0/0 | 4383 | 4 | 0 | 3 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0008c0011 | 0/0 | 4383 | 3 | 3 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0009c0020 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0009c0021 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0010c0012 | 0/0 | 4383 | 2 | 0 | 0 | 0 | 0 | 2 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0011c0014 | 0/0 | 4383 | 2 | 2 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0012c0016 | 0/0 | 4383 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0013c0018 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0014c0019 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0015c0017 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0016c0023 | 0/0 | 4383 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0017c0024 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0018c0039 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0019c0025 | 0/0 | 4383 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0020c0028 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0021c0033 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0022c0037 | 0/0 | 4383 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0023c0032 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0024c0030 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0025c0029 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0026c0035 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 5629 | 14 | 7 | 4 | 1 | 1 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0001c0002t0002 | 0/0 | 5629 | 69 | 4 | 15 | 39 | 3 | 8 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0001c0002t0003 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0001c0002t0004 | 0/0 | 5629 | 4 | 0 | 1 | 3 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0001c0002t0005 | 0/0 | 5629 | 3 | 0 | 0 | 3 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0001c0002t0022 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0001c0002t0023 | 0/0 | 5629 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0001c0005t0005 | 1/1 | 5629 | 33 | 1 | 6 | 15 | 1 | 8 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0001c0005t0016 | 0/0 | 5629 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0001c0005t0025 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0001c0013t0005 | 0/0 | 5629 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0001c0026t0002 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0001c0027t0002 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0001c0036t0005 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0002c0001t0001 | 0/0 | 5629 | 24 | 4 | 4 | 12 | 3 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0002c0001t0002 | 0/0 | 5629 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0002c0001t0003 | 0/0 | 5629 | 69 | 14 | 5 | 44 | 1 | 5 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0002c0001t0004 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0002c0001t0009 | 0/0 | 5629 | 4 | 2 | 2 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0002c0001t0024 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0002c0038t0003 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0003c0003t0002 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0003c0003t0004 | 0/0 | 5629 | 48 | 11 | 13 | 15 | 2 | 7 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0003c0003t0005 | 0/0 | 5629 | 8 | 7 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0003c0003t0011 | 0/0 | 5630 | 3 | 0 | 0 | 1 | 1 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0003c0003t0017 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0003c0022t0005 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0004c0004t0001 | 0/0 | 5629 | 34 | 11 | 7 | 14 | 0 | 2 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0004c0004t0010 | 0/0 | 5629 | 3 | 0 | 0 | 3 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0004c0004t0015 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0004c0004t0018 | 0/0 | 5629 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0004c0008t0001 | 0/0 | 5629 | 6 | 0 | 2 | 0 | 0 | 4 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0004c0009t0008 | 0/0 | 5629 | 4 | 1 | 0 | 0 | 2 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0004c0015t0003 | 0/0 | 5629 | 2 | 0 | 1 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0004c0031t0001 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0004c0034t0007 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0005c0006t0007 | 0/0 | 5629 | 5 | 5 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0005c0006t0008 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0006c0007t0006 | 0/0 | 5629 | 6 | 0 | 0 | 5 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0007c0010t0002 | 0/0 | 5629 | 4 | 0 | 3 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0008c0011t0007 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0008c0011t0012 | 0/0 | 5629 | 2 | 2 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0009c0020t0014 | 0/0 | 5630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0009c0021t0019 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0010c0012t0006 | 0/0 | 5629 | 2 | 0 | 0 | 0 | 0 | 2 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0011c0014t0013 | 0/0 | 5629 | 2 | 2 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0012c0016t0004 | 0/0 | 5629 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0013c0018t0014 | 0/0 | 5630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0014c0019t0004 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0015c0017t0004 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0016c0023t0006 | 0/0 | 5629 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0017c0024t0005 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0018c0039t0009 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0019c0025t0001 | 0/0 | 5629 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0020c0028t0004 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0021c0033t0001 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0022c0037t0005 | 0/0 | 5629 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0023c0032t0020 | 0/0 | 5630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0024c0030t0021 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0025c0029t0012 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
a0026c0035t0013 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | copy fasta | chr11 | 117322854 | 117418266 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0004g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0022g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0023g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0068 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0272 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0016g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0025g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0013t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0013t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0026t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0027t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0036t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0004 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0009g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0009g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0009g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0009g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0024g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0038t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0005g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0005g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0011g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0011g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0011g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0017g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0022t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0010g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0010g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0015g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0018g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0008t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0008t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0008t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0008t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0008t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0008t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0009t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0009t0008g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0009t0008g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0009t0008g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0015t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0015t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0031t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0034t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0005c0006t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0005c0006t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0005c0006t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0005c0006t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0005c0006t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0005c0006t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0006c0007t0006g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0006c0007t0006g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0006c0007t0006g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0006c0007t0006g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0006c0007t0006g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0006c0007t0006g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0007c0010t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0007c0010t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0007c0010t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0007c0010t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0008c0011t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0008c0011t0012g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0008c0011t0012g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0009c0020t0014g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0009c0021t0019g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0010c0012t0006g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0010c0012t0006g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0011c0014t0013g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0011c0014t0013g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0012c0016t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0013c0018t0014g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0014c0019t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0015c0017t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0016c0023t0006g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0017c0024t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0018c0039t0009g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0019c0025t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0020c0028t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0021c0033t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0022c0037t0005g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0023c0032t0020g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0024c0030t0021g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0025c0029t0012g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0026c0035t0013g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0001 | t0001 | g0180 | EUR | GBR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00099 | hp2 | a0003 | c0003 | t0004 | g0126 | EUR | GBR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00140 | hp1 | a0003 | c0003 | t0011 | g0123 | EUR | GBR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00140 | hp2 | a0002 | c0001 | t0003 | g0189 | EUR | GBR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0362 | EUR | FIN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00280 | hp2 | a0003 | c0003 | t0004 | g0074 | EUR | FIN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00323 | hp1 | a0004 | c0015 | t0003 | g0025 | EUR | FIN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00323 | hp2 | a0001 | c0002 | t0002 | g0345 | EUR | FIN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00408 | hp1 | a0003 | c0003 | t0004 | g0139 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00408 | hp2 | a0002 | c0001 | t0003 | g0262 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00423 | hp1 | a0002 | c0001 | t0003 | g0195 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00423 | hp2 | a0001 | c0005 | t0005 | g0173 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00438 | hp1 | a0002 | c0001 | t0003 | g0222 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00544 | hp1 | a0002 | c0038 | t0003 | g0203 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0144 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00558 | hp2 | a0002 | c0001 | t0003 | g0220 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00597 | hp1 | a0002 | c0001 | t0003 | g0198 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00597 | hp2 | a0006 | c0007 | t0006 | g0265 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0149 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00609 | hp2 | a0002 | c0001 | t0003 | g0221 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0360 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00621 | hp2 | a0002 | c0001 | t0003 | g0197 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00639 | hp1 | a0003 | c0003 | t0004 | g0228 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00639 | hp2 | a0004 | c0004 | t0001 | g0288 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00738 | hp1 | a0004 | c0004 | t0001 | g0305 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00738 | hp2 | a0001 | c0002 | t0004 | g0069 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00741 | hp1 | a0003 | c0003 | t0004 | g0230 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00741 | hp2 | a0002 | c0001 | t0001 | g0053 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01069 | hp1 | a0002 | c0001 | t0003 | g0218 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01069 | hp2 | a0001 | c0002 | t0023 | g0242 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0346 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01070 | hp2 | a0002 | c0001 | t0003 | g0187 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01071 | hp1 | a0002 | c0001 | t0003 | g0214 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01071 | hp2 | a0002 | c0001 | t0003 | g0188 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01074 | hp1 | a0002 | c0001 | t0009 | g0192 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01074 | hp2 | a0007 | c0010 | t0002 | g0168 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01081 | hp1 | a0007 | c0010 | t0002 | g0167 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01081 | hp2 | a0004 | c0004 | t0001 | g0295 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01099 | hp1 | a0004 | c0004 | t0001 | g0296 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01099 | hp2 | a0001 | c0005 | t0005 | g0085 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01106 | hp1 | a0002 | c0001 | t0001 | g0056 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01106 | hp2 | a0001 | c0005 | t0005 | g0055 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01109 | hp1 | a0004 | c0004 | t0001 | g0287 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01109 | hp2 | a0001 | c0005 | t0005 | g0355 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01167 | hp1 | a0003 | c0003 | t0004 | g0130 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0253 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01168 | hp1 | a0002 | c0001 | t0001 | g0090 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01168 | hp2 | a0001 | c0005 | t0005 | g0276 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01175 | hp2 | a0002 | c0001 | t0001 | g0091 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01243 | hp1 | a0002 | c0001 | t0009 | g0257 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01243 | hp2 | a0007 | c0010 | t0002 | g0174 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01257 | hp1 | a0004 | c0004 | t0001 | g0300 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0142 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01261 | hp2 | a0003 | c0003 | t0005 | g0007 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01346 | hp1 | a0001 | c0005 | t0005 | g0329 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0018 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01358 | hp1 | a0003 | c0003 | t0004 | g0052 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01358 | hp2 | a0004 | c0004 | t0001 | g0332 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0240 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01361 | hp2 | a0004 | c0008 | t0001 | g0297 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01433 | hp1 | a0004 | c0008 | t0001 | g0298 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01433 | hp2 | a0003 | c0003 | t0004 | g0231 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0071 | EUR | IBS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01515 | hp2 | a0007 | c0010 | t0002 | g0181 | EUR | IBS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0018 | EUR | IBS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01516 | hp2 | a0002 | c0001 | t0001 | g0054 | EUR | IBS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01884 | hp1 | a0004 | c0009 | t0008 | g0021 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01884 | hp2 | a0004 | c0004 | t0001 | g0015 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0235 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01928 | hp2 | a0003 | c0003 | t0004 | g0224 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01934 | hp1 | a0004 | c0015 | t0003 | g0024 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01934 | hp2 | a0001 | c0005 | t0005 | g0172 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0017 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01952 | hp2 | a0003 | c0003 | t0004 | g0133 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0252 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0352 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01978 | hp1 | a0003 | c0003 | t0004 | g0229 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0350 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0357 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01981 | hp2 | a0003 | c0003 | t0004 | g0110 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0017 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01993 | hp2 | a0002 | c0001 | t0003 | g0213 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02004 | hp1 | a0003 | c0003 | t0004 | g0109 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0145 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02027 | hp1 | a0002 | c0001 | t0001 | g0060 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02040 | hp1 | a0001 | c0002 | t0003 | g0177 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0152 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02055 | hp1 | a0005 | c0006 | t0007 | g0077 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02055 | hp2 | a0002 | c0001 | t0003 | g0255 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02056 | hp1 | a0002 | c0001 | t0001 | g0062 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0314 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02074 | hp1 | a0002 | c0001 | t0001 | g0061 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02074 | hp2 | a0001 | c0013 | t0005 | g0279 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02080 | hp1 | a0001 | c0026 | t0002 | g0154 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02080 | hp2 | a0002 | c0001 | t0003 | g0258 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02083 | hp2 | a0003 | c0003 | t0004 | g0131 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02132 | hp1 | a0002 | c0001 | t0002 | g0324 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02132 | hp2 | a0002 | c0001 | t0004 | g0196 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0166 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02135 | hp2 | a0003 | c0003 | t0017 | g0233 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0334 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02145 | hp2 | a0004 | c0034 | t0007 | g0039 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02155 | hp1 | a0004 | c0004 | t0001 | g0315 | EAS | CDX | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02155 | hp2 | a0001 | c0005 | t0005 | g0162 | EAS | CDX | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02165 | hp1 | a0002 | c0001 | t0001 | g0072 | EAS | CDX | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CDX | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02257 | hp1 | a0003 | c0003 | t0004 | g0113 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02257 | hp2 | a0004 | c0004 | t0001 | g0293 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02258 | hp1 | a0014 | c0019 | t0004 | g0051 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02258 | hp2 | a0002 | c0001 | t0003 | g0191 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02273 | hp1 | a0003 | c0003 | t0004 | g0006 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0347 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02280 | hp1 | a0004 | c0004 | t0001 | g0318 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02280 | hp2 | a0001 | c0002 | t0022 | g0343 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02293 | hp1 | a0003 | c0003 | t0004 | g0006 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0338 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0238 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02300 | hp2 | a0003 | c0003 | t0004 | g0120 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02451 | hp1 | a0024 | c0030 | t0021 | g0038 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02451 | hp2 | a0005 | c0006 | t0007 | g0049 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02572 | hp1 | a0003 | c0003 | t0005 | g0309 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02572 | hp2 | a0025 | c0029 | t0012 | g0079 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0348 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02602 | hp2 | a0019 | c0025 | t0001 | g0303 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02615 | hp1 | a0004 | c0004 | t0015 | g0016 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0036 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02630 | hp1 | a0011 | c0014 | t0013 | g0183 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0043 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02647 | hp1 | a0004 | c0004 | t0001 | g0016 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02647 | hp2 | a0003 | c0003 | t0005 | g0328 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02683 | hp1 | a0004 | c0009 | t0008 | g0022 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02683 | hp2 | a0003 | c0003 | t0004 | g0121 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02698 | hp1 | a0001 | c0005 | t0005 | g0158 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02698 | hp2 | a0003 | c0003 | t0004 | g0106 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02717 | hp1 | a0004 | c0031 | t0001 | g0292 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02717 | hp2 | a0003 | c0003 | t0005 | g0007 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02723 | hp1 | a0002 | c0001 | t0003 | g0097 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02723 | hp2 | a0003 | c0003 | t0004 | g0112 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02735 | hp1 | a0004 | c0008 | t0001 | g0301 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02735 | hp2 | a0012 | c0016 | t0004 | g0122 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0237 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02738 | hp2 | a0002 | c0001 | t0001 | g0063 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02809 | hp1 | a0002 | c0001 | t0003 | g0134 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02809 | hp2 | a0002 | c0001 | t0001 | g0058 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02818 | hp1 | a0003 | c0003 | t0004 | g0225 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02818 | hp2 | a0011 | c0014 | t0013 | g0254 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02886 | hp1 | a0002 | c0001 | t0009 | g0184 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02895 | hp1 | a0018 | c0039 | t0009 | g0200 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02896 | hp1 | a0001 | c0002 | t0002 | g0340 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02896 | hp2 | a0003 | c0003 | t0005 | g0117 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02897 | hp1 | a0003 | c0003 | t0005 | g0083 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02922 | hp1 | a0005 | c0006 | t0008 | g0045 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02922 | hp2 | a0002 | c0001 | t0003 | g0010 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02970 | hp1 | a0004 | c0004 | t0001 | g0302 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02970 | hp2 | a0003 | c0003 | t0004 | g0124 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02976 | hp2 | a0005 | c0006 | t0007 | g0075 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03017 | hp1 | a0002 | c0001 | t0003 | g0095 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0087 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03041 | hp1 | a0002 | c0001 | t0003 | g0234 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03041 | hp2 | a0023 | c0032 | t0020 | g0193 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03098 | hp1 | a0005 | c0006 | t0007 | g0048 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03098 | hp2 | a0015 | c0017 | t0004 | g0182 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03130 | hp1 | a0021 | c0033 | t0001 | g0286 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03130 | hp2 | a0008 | c0011 | t0012 | g0080 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03139 | hp1 | a0002 | c0001 | t0003 | g0010 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03139 | hp2 | a0002 | c0001 | t0009 | g0256 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0341 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03209 | hp2 | a0002 | c0001 | t0003 | g0199 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03225 | hp1 | a0004 | c0004 | t0001 | g0291 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03225 | hp2 | a0026 | c0035 | t0013 | g0046 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03239 | hp1 | a0004 | c0004 | t0001 | g0304 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03239 | hp2 | a0003 | c0003 | t0004 | g0104 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03453 | hp1 | a0001 | c0005 | t0005 | g0331 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03453 | hp2 | a0003 | c0003 | t0005 | g0116 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03486 | hp1 | a0002 | c0001 | t0003 | g0363 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03486 | hp2 | a0004 | c0004 | t0001 | g0294 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03490 | hp1 | a0002 | c0001 | t0003 | g0011 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03490 | hp2 | a0004 | c0004 | t0001 | g0289 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03491 | hp1 | a0004 | c0008 | t0001 | g0307 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03491 | hp2 | a0002 | c0001 | t0003 | g0094 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03492 | hp1 | a0002 | c0001 | t0003 | g0011 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03492 | hp2 | a0004 | c0008 | t0001 | g0308 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03516 | hp1 | a0002 | c0001 | t0003 | g0135 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03516 | hp2 | a0002 | c0001 | t0003 | g0364 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03540 | hp1 | a0002 | c0001 | t0001 | g0057 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03540 | hp2 | a0003 | c0003 | t0004 | g0098 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03579 | hp1 | a0003 | c0003 | t0004 | g0114 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03579 | hp2 | a0008 | c0011 | t0012 | g0081 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0147 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03654 | hp2 | a0003 | c0003 | t0004 | g0223 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0169 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03669 | hp2 | a0001 | c0005 | t0016 | g0273 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03688 | hp1 | a0001 | c0005 | t0005 | g0277 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0306 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03704 | hp1 | a0002 | c0001 | t0003 | g0096 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03704 | hp2 | a0010 | c0012 | t0006 | g0268 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03710 | hp1 | a0010 | c0012 | t0006 | g0266 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03710 | hp2 | a0001 | c0005 | t0005 | g0033 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03831 | hp1 | a0003 | c0003 | t0004 | g0108 | SAS | BEB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03831 | hp2 | a0001 | c0005 | t0005 | g0244 | SAS | BEB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03834 | hp1 | a0003 | c0003 | t0011 | g0119 | SAS | BEB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03834 | hp2 | a0016 | c0023 | t0006 | g0031 | SAS | BEB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0153 | SAS | BEB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03927 | hp2 | a0001 | c0005 | t0005 | g0275 | SAS | BEB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0247 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04115 | hp2 | a0001 | c0005 | t0005 | g0278 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04184 | hp1 | a0001 | c0005 | t0005 | g0032 | SAS | BEB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04184 | hp2 | a0003 | c0003 | t0004 | g0107 | SAS | BEB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04199 | hp1 | a0006 | c0007 | t0006 | g0030 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04199 | hp2 | a0004 | c0008 | t0001 | g0299 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04204 | hp1 | a0001 | c0005 | t0005 | g0281 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0044 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04228 | hp1 | a0003 | c0003 | t0004 | g0105 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04228 | hp2 | a0004 | c0004 | t0018 | g0313 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0317 | AFR | YRI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18522 | hp2 | a0003 | c0003 | t0005 | g0118 | AFR | YRI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18612 | hp1 | a0002 | c0001 | t0003 | g0354 | EAS | CHB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18612 | hp2 | a0002 | c0001 | t0003 | g0207 | EAS | CHB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18906 | hp1 | a0001 | c0005 | t0025 | g0078 | AFR | YRI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18906 | hp2 | a0003 | c0003 | t0004 | g0129 | AFR | YRI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18940 | hp1 | a0001 | c0002 | t0005 | g0165 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18940 | hp2 | a0002 | c0001 | t0003 | g0264 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0321 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18944 | hp2 | a0020 | c0028 | t0004 | g0155 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18945 | hp1 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18945 | hp2 | a0004 | c0004 | t0001 | g0093 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18946 | hp1 | a0001 | c0005 | t0005 | g0159 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18946 | hp2 | a0002 | c0001 | t0003 | g0205 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18948 | hp1 | a0002 | c0001 | t0001 | g0280 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18948 | hp2 | a0001 | c0002 | t0002 | g0319 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18950 | hp1 | a0001 | c0005 | t0005 | g0160 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18950 | hp2 | a0002 | c0001 | t0003 | g0219 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18954 | hp1 | a0002 | c0001 | t0003 | g0066 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18954 | hp2 | a0001 | c0002 | t0005 | g0151 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18956 | hp1 | a0006 | c0007 | t0006 | g0270 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18957 | hp1 | a0002 | c0001 | t0001 | g0283 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18957 | hp2 | a0001 | c0005 | t0005 | g0146 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18959 | hp1 | a0004 | c0004 | t0001 | g0047 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18959 | hp2 | a0001 | c0002 | t0002 | g0337 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18960 | hp1 | a0003 | c0003 | t0004 | g0127 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18960 | hp2 | a0001 | c0005 | t0005 | g0143 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18964 | hp1 | a0003 | c0003 | t0004 | g0103 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0351 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18966 | hp1 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18966 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18967 | hp1 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18967 | hp2 | a0002 | c0001 | t0003 | g0179 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18968 | hp1 | a0004 | c0004 | t0001 | g0312 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18970 | hp1 | a0001 | c0005 | t0005 | g0243 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18971 | hp2 | a0002 | c0001 | t0003 | g0259 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18972 | hp1 | a0004 | c0004 | t0001 | g0311 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18972 | hp2 | a0003 | c0003 | t0004 | g0034 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18973 | hp1 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18973 | hp2 | a0002 | c0001 | t0003 | g0201 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18974 | hp1 | a0002 | c0001 | t0003 | g0185 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18974 | hp2 | a0002 | c0001 | t0003 | g0178 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18975 | hp1 | a0002 | c0001 | t0001 | g0013 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18975 | hp2 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18977 | hp2 | a0001 | c0036 | t0005 | g0161 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18978 | hp1 | a0001 | c0005 | t0005 | g0250 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18978 | hp2 | a0006 | c0007 | t0006 | g0271 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18979 | hp2 | a0003 | c0003 | t0011 | g0232 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18980 | hp1 | a0001 | c0002 | t0004 | g0239 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18980 | hp2 | a0003 | c0003 | t0002 | g0128 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0339 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18982 | hp2 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18983 | hp1 | a0001 | c0005 | t0005 | g0009 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0336 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0322 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18986 | hp2 | a0002 | c0001 | t0003 | g0194 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18988 | hp1 | a0003 | c0003 | t0004 | g0132 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18988 | hp2 | a0002 | c0001 | t0003 | g0217 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18989 | hp1 | a0002 | c0001 | t0003 | g0261 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18989 | hp2 | a0004 | c0004 | t0010 | g0073 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18990 | hp1 | a0002 | c0001 | t0003 | g0212 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18990 | hp2 | a0001 | c0005 | t0005 | g0084 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18991 | hp1 | a0003 | c0003 | t0004 | g0099 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18991 | hp2 | a0002 | c0001 | t0003 | g0260 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18992 | hp1 | a0002 | c0001 | t0003 | g0211 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18992 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18995 | hp1 | a0001 | c0002 | t0004 | g0361 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18995 | hp2 | a0002 | c0001 | t0002 | g0156 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18998 | hp1 | a0001 | c0005 | t0005 | g0249 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0358 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18999 | hp1 | a0002 | c0001 | t0003 | g0216 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19000 | hp2 | a0002 | c0001 | t0003 | g0263 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19001 | hp1 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19001 | hp2 | a0001 | c0005 | t0005 | g0163 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19002 | hp1 | a0003 | c0003 | t0004 | g0138 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19002 | hp2 | a0004 | c0004 | t0010 | g0003 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19003 | hp1 | a0002 | c0001 | t0001 | g0284 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19003 | hp2 | a0003 | c0003 | t0004 | g0140 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19004 | hp1 | a0002 | c0001 | t0003 | g0204 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19004 | hp2 | a0004 | c0004 | t0010 | g0003 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19007 | hp1 | a0002 | c0001 | t0001 | g0013 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19010 | hp1 | a0004 | c0004 | t0001 | g0067 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0320 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19011 | hp1 | a0017 | c0024 | t0005 | g0141 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19012 | hp1 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0323 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19030 | hp1 | a0004 | c0004 | t0001 | g0310 | AFR | LWK | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19030 | hp2 | a0013 | c0018 | t0014 | g0269 | AFR | LWK | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19043 | hp1 | a0002 | c0001 | t0024 | g0089 | AFR | LWK | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19043 | hp2 | a0003 | c0003 | t0004 | g0100 | AFR | LWK | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19054 | hp1 | a0003 | c0003 | t0004 | g0035 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19054 | hp2 | a0006 | c0007 | t0006 | g0267 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0349 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19056 | hp2 | a0001 | c0005 | t0005 | g0086 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19057 | hp1 | a0004 | c0004 | t0001 | g0065 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19057 | hp2 | a0002 | c0001 | t0003 | g0209 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19058 | hp1 | a0003 | c0003 | t0004 | g0101 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19058 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19060 | hp1 | a0003 | c0003 | t0004 | g0136 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19060 | hp2 | a0001 | c0002 | t0005 | g0241 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19062 | hp1 | a0002 | c0001 | t0003 | g0012 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19062 | hp2 | a0003 | c0003 | t0004 | g0111 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19067 | hp1 | a0002 | c0001 | t0003 | g0186 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19067 | hp2 | a0002 | c0001 | t0003 | g0092 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19074 | hp1 | a0004 | c0004 | t0001 | g0064 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19074 | hp2 | a0001 | c0002 | t0002 | g0335 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19075 | hp1 | a0004 | c0004 | t0001 | g0333 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19075 | hp2 | a0001 | c0002 | t0004 | g0157 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19077 | hp1 | a0006 | c0007 | t0006 | g0029 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19077 | hp2 | a0001 | c0005 | t0005 | g0009 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19078 | hp1 | a0002 | c0001 | t0003 | g0206 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19078 | hp2 | a0001 | c0005 | t0005 | g0251 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19079 | hp1 | a0002 | c0001 | t0003 | g0208 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0359 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19080 | hp1 | a0003 | c0003 | t0004 | g0102 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19080 | hp2 | a0002 | c0001 | t0003 | g0176 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0353 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19081 | hp2 | a0002 | c0001 | t0003 | g0215 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19085 | hp1 | a0003 | c0003 | t0004 | g0137 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19085 | hp2 | a0002 | c0001 | t0003 | g0325 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19087 | hp1 | a0004 | c0004 | t0001 | g0027 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19087 | hp2 | a0002 | c0001 | t0003 | g0012 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19088 | hp1 | a0002 | c0001 | t0003 | g0202 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19090 | hp1 | a0002 | c0001 | t0003 | g0210 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19090 | hp2 | a0004 | c0004 | t0001 | g0316 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19240 | hp1 | a0003 | c0003 | t0004 | g0226 | AFR | YRI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19240 | hp2 | a0002 | c0001 | t0003 | g0356 | AFR | YRI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA20129 | hp1 | a0008 | c0011 | t0007 | g0028 | AFR | ASW | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA20129 | hp2 | a0002 | c0001 | t0001 | g0059 | AFR | ASW | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA20752 | hp1 | a0004 | c0009 | t0008 | g0026 | EUR | TSI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA20752 | hp2 | a0002 | c0001 | t0001 | g0004 | EUR | TSI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA20805 | hp1 | a0004 | c0009 | t0008 | g0023 | EUR | TSI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA20805 | hp2 | a0001 | c0005 | t0005 | g0274 | EUR | TSI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01123 | hp1 | a0022 | c0037 | t0005 | g0330 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02109 | hp1 | a0004 | c0004 | t0001 | g0015 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02109 | hp2 | a0005 | c0006 | t0007 | g0076 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02486 | hp1 | a0003 | c0003 | t0004 | g0125 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02486 | hp2 | a0001 | c0027 | t0002 | g0342 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02559 | hp1 | a0009 | c0020 | t0014 | g0327 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02559 | hp2 | a0004 | c0004 | t0001 | g0285 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03471 | hp1 | a0003 | c0003 | t0004 | g0115 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03471 | hp2 | a0004 | c0004 | t0001 | g0290 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG06807 | hp1 | a0002 | c0001 | t0003 | g0190 | AFR | USA | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG06807 | hp2 | a0009 | c0021 | t0019 | g0082 | AFR | USA | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18955 | hp1 | a0002 | c0001 | t0001 | g0282 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18955 | hp2 | a0001 | c0013 | t0005 | g0236 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0344 | AFR | USA | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA20300 | hp2 | a0003 | c0022 | t0005 | g0227 | AFR | USA | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA21309 | hp1 | a0002 | c0001 | t0001 | g0004 | AFR | LWK | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA21309 | hp2 | a0002 | c0001 | t0003 | g0365 | AFR | LWK | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
homoSapiens_chm13v2 | hp1 | a0001 | c0005 | t0005 | g0272 | REF | REF | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
homoSapiens_grch38 | hp1 | a0001 | c0005 | t0005 | g0068 | REF | REF | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:117351876
|
G | A | 10 | a0003a0005a0006others(7): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
missense_variant | MODERATE | c.281G>A | p.Ser94Asn | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/33 | 429/5629 | 281/4383 | 94/1460 | chr11 | 117351876 | ||
chr11:117361893
|
G | A | 1 | a0017 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.452G>A | p.Arg151Gln | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 6/33 | 600/5629 | 452/4383 | 151/1460 | chr11 | 117361893 | ||
chr11:117361898
|
C | T | 1 | a0018 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.457C>T | p.Leu153Phe | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 6/33 | 605/5629 | 457/4383 | 153/1460 | chr11 | 117361898 | ||
chr11:117361989
|
T | A | 1 | a0019 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.548T>A | p.Met183Lys | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 6/33 | 696/5629 | 548/4383 | 183/1460 | chr11 | 117361989 | ||
chr11:117381721
|
A | G | 1 | a0007 | 4 | HG01074.hp2 HG01081.hp1 HG01243.hp2 others(1): Show |
missense_variant | MODERATE | c.1430A>G | p.His477Arg | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 13/33 | 1578/5629 | 1430/4383 | 477/1460 | chr11 | 117381721 | ||
chr11:117381775
|
C | G | 3 | a0006a0010a0016 | 9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
missense_variant | MODERATE | c.1484C>G | p.Pro495Arg | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 13/33 | 1632/5629 | 1484/4383 | 495/1460 | chr11 | 117381775 | ||
chr11:117382909
|
C | T | 1 | a0026 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.1691C>T | p.Ala564Val | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/33 | 1839/5629 | 1691/4383 | 564/1460 | chr11 | 117382909 | ||
chr11:117393037
|
G | A | 1 | a0012 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.2527G>A | p.Val843Met | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/33 | 2675/5629 | 2527/4383 | 843/1460 | chr11 | 117393037 | ||
chr11:117395136
|
G | A | 1 | a0020 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.2858G>A | p.Arg953Gln | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 23/33 | 3006/5629 | 2858/4383 | 953/1460 | chr11 | 117395136 | ||
chr11:117395596
|
C | G | 2 | a0002a0018 | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(100): Show |
missense_variant | MODERATE | c.2963C>G | p.Thr988Ser | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 24/33 | 3111/5629 | 2963/4383 | 988/1460 | chr11 | 117395596 | ||
chr11:117395652
|
C | T | 1 | a0021 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.3019C>T | p.Arg1007Cys | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 24/33 | 3167/5629 | 3019/4383 | 1007/1460 | chr11 | 117395652 | ||
chr11:117395665
|
T | C | 1 | a0015 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.3032T>C | p.Leu1011Pro | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 24/33 | 3180/5629 | 3032/4383 | 1011/1460 | chr11 | 117395665 | ||
chr11:117397144
|
G | A | 1 | a0013 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.3332G>A | p.Arg1111His | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/33 | 3480/5629 | 3332/4383 | 1111/1460 | chr11 | 117397144 | ||
chr11:117397168
|
A | G | 15 | a0002a0004a0005others(12): Show | 182 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
missense_variant | MODERATE | c.3356A>G | p.Gln1119Arg | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/33 | 3504/5629 | 3356/4383 | 1119/1460 | chr11 | 117397168 | ||
chr11:117397176
|
C | T | 1 | a0010 | 2 | HG03704.hp2 HG03710.hp1 |
missense_variant | MODERATE | c.3364C>T | p.Arg1122Cys | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/33 | 3512/5629 | 3364/4383 | 1122/1460 | chr11 | 117397176 | ||
chr11:117397177
|
G | A | 1 | a0014 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.3365G>A | p.Arg1122His | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/33 | 3513/5629 | 3365/4383 | 1122/1460 | chr11 | 117397177 | ||
chr11:117408996
|
C | T | 7 | a0006a0009a0010others(4): Show | 15 | HG00597.hp2 HG02559.hp1 HG02630.hp1 others(12): Show |
missense_variant | MODERATE | c.3716C>T | p.Pro1239Leu | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 29/33 | 3864/5629 | 3716/4383 | 1239/1460 | chr11 | 117408996 | ||
chr11:117409642
|
C | T | 1 | a0024 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.3773C>T | p.Ser1258Phe | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/33 | 3921/5629 | 3773/4383 | 1258/1460 | chr11 | 117409642 | ||
chr11:117409773
|
C | T | 1 | a0022 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.3904C>T | p.Pro1302Ser | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/33 | 4052/5629 | 3904/4383 | 1302/1460 | chr11 | 117409773 | ||
chr11:117409801
|
C | G | 5 | a0008a0009a0013others(2): Show | 8 | HG02559.hp1 HG02572.hp2 HG03041.hp2 others(5): Show |
missense_variant | MODERATE | c.3932C>G | p.Thr1311Ser | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/33 | 4080/5629 | 3932/4383 | 1311/1460 | chr11 | 117409801 | ||
chr11:117409894
|
C | T | 1 | a0025 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.4025C>T | p.Pro1342Leu | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/33 | 4173/5629 | 4025/4383 | 1342/1460 | chr11 | 117409894 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:117371142
|
C | T | 1 | a0002c0038 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.828C>T | p.Ala276Ala | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/33 | 976/5629 | 828/4383 | 276/1460 | chr11 | 117371142 | ||
chr11:117380676
|
G | A | 1 | a0001c0026 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.1380G>A | p.Gln460Gln | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/33 | 1528/5629 | 1380/4383 | 460/1460 | chr11 | 117380676 | ||
chr11:117381773
|
T | C | 34 | a0001c0002a0001c0013a0001c0026others(31): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
synonymous_variant | LOW | c.1482T>C | p.Pro494Pro | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 13/33 | 1630/5629 | 1482/4383 | 494/1460 | chr11 | 117381773 | ||
chr11:117382925
|
G | T | 1 | a0003c0022 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.1707G>T | p.Pro569Pro | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/33 | 1855/5629 | 1707/4383 | 569/1460 | chr11 | 117382925 | ||
chr11:117391137
|
C | T | 2 | a0004c0009a0004c0015 | 6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
synonymous_variant | LOW | c.2205C>T | p.Ser735Ser | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 17/33 | 2353/5629 | 2205/4383 | 735/1460 | chr11 | 117391137 | ||
chr11:117392243
|
G | A | 1 | a0001c0027 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.2301G>A | p.Glu767Glu | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 18/33 | 2449/5629 | 2301/4383 | 767/1460 | chr11 | 117392243 | ||
chr11:117394388
|
C | T | 1 | a0004c0034 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.2655C>T | p.Thr885Thr | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 21/33 | 2803/5629 | 2655/4383 | 885/1460 | chr11 | 117394388 | ||
chr11:117396558
|
C | T | 2 | a0009c0021a0023c0032 | 2 | HG03041.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.3225C>T | p.Thr1075Thr | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 26/33 | 3373/5629 | 3225/4383 | 1075/1460 | chr11 | 117396558 | ||
chr11:117407979
|
C | T | 1 | a0004c0031 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.3556C>T | p.Leu1186Leu | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 28/33 | 3704/5629 | 3556/4383 | 1186/1460 | chr11 | 117407979 | ||
chr11:117409796
|
C | T | 7 | a0008c0011a0009c0020a0009c0021others(4): Show | 9 | HG02559.hp1 HG02572.hp2 HG03041.hp2 others(6): Show |
synonymous_variant | LOW | c.3927C>T | p.Thr1309Thr | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/33 | 4075/5629 | 3927/4383 | 1309/1460 | chr11 | 117409796 | ||
chr11:117410850
|
C | T | 1 | a0004c0008 | 6 | HG01361.hp2 HG01433.hp1 HG02735.hp1 others(3): Show |
synonymous_variant | LOW | c.4119C>T | p.Asn1373Asn | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 31/33 | 4267/5629 | 4119/4383 | 1373/1460 | chr11 | 117410850 | ||
chr11:117410862
|
G | A | 1 | a0009c0021 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.4131G>A | p.Pro1377Pro | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 31/33 | 4279/5629 | 4131/4383 | 1377/1460 | chr11 | 117410862 | ||
chr11:117410862
|
G | T | 1 | a0001c0036 | 1 | NA18977.hp2 | synonymous_variant | LOW | c.4131G>T | p.Pro1377Pro | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 31/33 | 4279/5629 | 4131/4383 | 1377/1460 | chr11 | 117410862 | ||
chr11:117412084
|
G | T | 34 | a0001c0002a0001c0026a0001c0027others(31): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
synonymous_variant | LOW | c.4299G>T | p.Ser1433Ser | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 4447/5629 | 4299/4383 | 1433/1460 | chr11 | 117412084 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:117327893
|
C | T | 3 | a0001c0005t0025a0002c0001t0009a0018c0039t0009 | 6 | HG01074.hp1 HG01243.hp1 HG02886.hp1 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-109C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/33 | chr11 | 117327893 | ||||||
chr11:117412185
|
T | C | 1 | a0004c0004t0010 | 3 | NA18989.hp2 NA19002.hp2 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*17T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 17 | chr11 | 117412185 | |||||
chr11:117412226
|
G | A | 1 | a0004c0004t0015 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*58G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 58 | chr11 | 117412226 | |||||
chr11:117412263
|
C | G | 9 | a0001c0002t0003a0002c0001t0003a0002c0001t0009others(6): Show | 84 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*95C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 95 | chr11 | 117412263 | |||||
chr11:117412306
|
G | T | 1 | a0001c0002t0023 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*138G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 138 | chr11 | 117412306 | |||||
chr11:117412339
|
A | G | 1 | a0001c0002t0022 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*171A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 171 | chr11 | 117412339 | |||||
chr11:117412375
|
C | T | 31 | a0001c0002t0001a0001c0002t0002a0001c0002t0022others(28): Show | 190 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*207C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 207 | chr11 | 117412375 | |||||
chr11:117412425
|
C | T | 2 | a0008c0011t0012a0025c0029t0012 | 3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*257C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 257 | chr11 | 117412425 | |||||
chr11:117412755
|
C | T | 20 | a0001c0002t0003a0002c0001t0003a0002c0001t0009others(17): Show | 105 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*587C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 587 | chr11 | 117412755 | |||||
chr11:117412771
|
A | G | 1 | a0002c0001t0024 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*603A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 603 | chr11 | 117412771 | |||||
chr11:117412888
|
G | A | 2 | a0009c0021t0019a0023c0032t0020 | 2 | HG03041.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*720G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 720 | chr11 | 117412888 | |||||
chr11:117412910
|
A | G | 13 | a0001c0002t0003a0002c0001t0003a0002c0001t0009others(10): Show | 92 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*742A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 742 | chr11 | 117412910 | |||||
chr11:117412918
|
A | G | 13 | a0001c0002t0003a0002c0001t0003a0002c0001t0009others(10): Show | 92 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*750A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 750 | chr11 | 117412918 | |||||
chr11:117412927
|
A | G | 1 | a0024c0030t0021 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*759A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 759 | chr11 | 117412927 | |||||
chr11:117412948
|
T | C | 2 | a0011c0014t0013a0026c0035t0013 | 3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*780T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 780 | chr11 | 117412948 | |||||
chr11:117412960
|
T | C | 36 | a0001c0002t0001a0001c0002t0003a0001c0002t0023others(33): Show | 199 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*792T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 792 | chr11 | 117412960 | |||||
chr11:117413092
|
C | T | 9 | a0001c0002t0004a0002c0001t0004a0003c0003t0004others(6): Show | 61 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*924C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 924 | chr11 | 117413092 | |||||
chr11:117413105
|
A | G | 3 | a0006c0007t0006a0010c0012t0006a0016c0023t0006 | 9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*937A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 937 | chr11 | 117413105 | |||||
chr11:117413160
|
C | T | 1 | a0004c0004t0018 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*992C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 992 | chr11 | 117413160 | |||||
chr11:117413223
|
G | A | 5 | a0002c0001t0009a0004c0009t0008a0005c0006t0008others(2): Show | 11 | HG01074.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1055G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 1055 | chr11 | 117413223 | |||||
chr11:117413251
|
G | GT | 4 | a0003c0003t0011a0009c0020t0014a0013c0018t0014others(1): Show | 6 | HG00140.hp1 HG02559.hp1 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1094dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 1095 | INFO_REALIGN_3_PRIME | chr11 | 117413251 | ||||
chr11:117413252
|
T | G | 1 | a0003c0003t0017 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1084T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 1084 | chr11 | 117413252 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:117327922
|
T | C | 6 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(3): Show | 6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-98+18T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117327922 | ||||||
chr11:117327982
|
T | G | 1 | a0004c0004t0001g0027 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-98+78T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117327982 | ||||||
chr11:117328073
|
A | T | 89 | a0001c0002t0001g0306a0001c0002t0001g0317a0001c0002t0001g0326others(86): Show | 94 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.-98+169A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117328073 | ||||||
chr11:117328203
|
T | G | 1 | a0008c0011t0007g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-98+299T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117328203 | ||||||
chr11:117328258
|
C | T | 3 | a0002c0001t0003g0363a0002c0001t0003g0364a0002c0001t0003g0365 | 3 | HG03486.hp1 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-98+354C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117328258 | ||||||
chr11:117328448
|
T | C | 5 | a0001c0005t0005g0032a0001c0005t0005g0033a0006c0007t0006g0029others(2): Show | 5 | HG03710.hp2 HG03834.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.-98+544T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117328448 | ||||||
chr11:117328455
|
C | T | 5 | a0002c0001t0001g0013a0002c0001t0001g0014a0002c0001t0001g0282others(2): Show | 7 | NA18955.hp1 NA18957.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.-98+551C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117328455 | ||||||
chr11:117328601
|
C | T | 23 | a0001c0005t0005g0032a0001c0005t0005g0033a0001c0005t0005g0272others(20): Show | 23 | HG00597.hp2 HG01168.hp2 HG02074.hp2 others(20): Show |
intron_variant | MODIFIER | c.-98+697C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117328601 | ||||||
chr11:117328769
|
A | G | 1 | a0001c0005t0005g0033 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-98+865A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117328769 | ||||||
chr11:117328912
|
G | C | 2 | a0003c0003t0004g0034a0003c0003t0004g0035 | 2 | NA18972.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-98+1008G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117328912 | ||||||
chr11:117329026
|
T | G | 31 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(28): Show | 31 | HG00597.hp2 HG01168.hp2 HG02074.hp2 others(28): Show |
intron_variant | MODIFIER | c.-98+1122T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117329026 | ||||||
chr11:117329154
|
C | T | 126 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(123): Show | 131 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.-98+1250C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117329154 | ||||||
chr11:117329413
|
C | T | 1 | a0001c0002t0002g0362 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-98+1509C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117329413 | ||||||
chr11:117329580
|
C | T | 1 | a0008c0011t0007g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-98+1676C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117329580 | ||||||
chr11:117329726
|
G | C | 1 | a0001c0002t0002g0044 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-98+1822G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117329726 | ||||||
chr11:117329839
|
C | CT | 65 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0042others(62): Show | 69 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.-98+1958dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117329839 | |||||
chr11:117329839
|
C | CTT | 146 | a0001c0002t0001g0043a0001c0002t0002g0001a0001c0002t0002g0008others(143): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.-98+1957_-98+1958d others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117329839 | |||||
chr11:117329839
|
C | CTTT | 42 | a0001c0002t0001g0252a0001c0002t0001g0253a0001c0002t0002g0235others(39): Show | 42 | HG00408.hp2 HG00639.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.-98+1956_-98+1958d others(5): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117329839 | |||||
chr11:117329839
|
CT | C | 28 | a0001c0002t0001g0306a0004c0004t0001g0015a0004c0004t0001g0047others(25): Show | 29 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.-98+1958delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117329839 | |||||
chr11:117329862
|
T | A | 1 | a0001c0005t0005g0033 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-98+1958T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117329862 | ||||||
chr11:117329862
|
T | TA | 8 | a0001c0005t0005g0032a0006c0007t0006g0029a0006c0007t0006g0030others(5): Show | 8 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.-98+1960dupA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117329862 | |||||
chr11:117329922
|
T | A | 41 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(38): Show | 41 | HG00323.hp1 HG00597.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.-98+2018T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117329922 | ||||||
chr11:117330037
|
T | G | 41 | a0001c0002t0001g0306a0001c0002t0001g0317a0001c0002t0001g0334others(38): Show | 42 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.-98+2133T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330037 | ||||||
chr11:117330046
|
T | C | 1 | a0001c0002t0001g0050 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-98+2142T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330046 | ||||||
chr11:117330227
|
T | G | 266 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(263): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-98+2323T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330227 | ||||||
chr11:117330258
|
C | T | 3 | a0001c0002t0001g0050a0001c0002t0001g0252a0001c0002t0001g0253 | 3 | HG01167.hp2 HG01175.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.-98+2354C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330258 | ||||||
chr11:117330340
|
T | A | 8 | a0001c0002t0001g0037a0001c0002t0001g0050a0001c0002t0001g0252others(5): Show | 8 | HG01167.hp2 HG01175.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.-98+2436T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330340 | ||||||
chr11:117330362
|
G | A | 1 | a0026c0035t0013g0046 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-98+2458G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330362 | ||||||
chr11:117330381
|
G | T | 162 | a0001c0002t0001g0306a0001c0002t0001g0317a0001c0002t0001g0326others(159): Show | 172 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.-98+2477G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330381 | ||||||
chr11:117330449
|
T | G | 90 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0042others(87): Show | 92 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.-98+2545T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330449 | ||||||
chr11:117330450
|
C | G | 1 | a0004c0004t0001g0318 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-98+2546C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330450 | ||||||
chr11:117330506
|
G | A | 1 | a0017c0024t0005g0141 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-98+2602G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330506 | ||||||
chr11:117330584
|
G | A | 1 | a0002c0001t0001g0053 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-98+2680G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330584 | ||||||
chr11:117330643
|
C | CT | 3 | a0002c0001t0003g0220a0002c0001t0003g0221a0002c0001t0003g0222 | 3 | HG00438.hp1 HG00558.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.-98+2740dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117330643 | |||||
chr11:117330649
|
CA | C | 66 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0042others(63): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.-98+2754delA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117330649 | |||||
chr11:117330688
|
A | G | 2 | a0004c0008t0001g0307a0004c0008t0001g0308 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-98+2784A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330688 | ||||||
chr11:117330742
|
A | G | 32 | a0002c0001t0003g0012a0002c0001t0003g0094a0002c0001t0003g0095others(29): Show | 33 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.-98+2838A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330742 | ||||||
chr11:117330746
|
A | T | 1 | a0004c0004t0010g0073 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-98+2842A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330746 | ||||||
chr11:117330788
|
T | C | 1 | a0002c0001t0024g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-98+2884T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330788 | ||||||
chr11:117330954
|
A | G | 3 | a0001c0002t0001g0037a0001c0002t0001g0317a0001c0002t0001g0334 | 3 | HG02145.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-98+3050A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330954 | ||||||
chr11:117330966
|
T | C | 268 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(265): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-98+3062T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330966 | ||||||
chr11:117331033
|
C | G | 74 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0042others(71): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-98+3129C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117331033 | ||||||
chr11:117331047
|
G | A | 1 | a0001c0002t0002g0142 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-98+3143G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117331047 | ||||||
chr11:117331255
|
A | G | 3 | a0011c0014t0013g0183a0011c0014t0013g0254a0026c0035t0013g0046 | 3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-98+3351A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117331255 | ||||||
chr11:117331281
|
C | T | 174 | a0001c0002t0001g0037a0001c0002t0001g0050a0001c0002t0001g0252others(171): Show | 184 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.-98+3377C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117331281 | ||||||
chr11:117331430
|
C | CA | 268 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(265): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-98+3526_-98+3527i others(3): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117331430 | ||||||
chr11:117331643
|
C | T | 1 | a0002c0001t0001g0072 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-98+3739C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117331643 | ||||||
chr11:117331721
|
G | A | 174 | a0001c0002t0001g0037a0001c0002t0001g0050a0001c0002t0001g0252others(171): Show | 184 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.-98+3817G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117331721 | ||||||
chr11:117331750
|
A | AT | 71 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0042others(68): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-97-3841dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117331750 | |||||
chr11:117331750
|
AT | A | 7 | a0002c0001t0001g0004a0002c0001t0001g0054a0002c0001t0001g0057others(4): Show | 8 | HG01168.hp1 HG01175.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.-97-3841delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117331750 | |||||
chr11:117331827
|
G | A | 1 | a0009c0021t0019g0082 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-97-3778G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117331827 | ||||||
chr11:117331918
|
CA | C | 5 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-97-3686delA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117331918 | ||||||
chr11:117331981
|
A | AAT | 228 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(225): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.-97-3603_-97-3602d others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117331981 | |||||
chr11:117331981
|
A | AATAT | 22 | a0001c0002t0001g0306a0001c0002t0002g0044a0001c0002t0002g0235others(19): Show | 22 | HG00639.hp2 HG01109.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.-97-3605_-97-3602d others(6): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117331981 | |||||
chr11:117331981
|
A | AATATAT | 44 | a0002c0001t0003g0002a0002c0001t0003g0011a0002c0001t0003g0096others(41): Show | 48 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.-97-3607_-97-3602d others(8): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117331981 | |||||
chr11:117331981
|
A | AATATATA others(1): Show |
12 | a0002c0001t0003g0010a0002c0001t0003g0012a0002c0001t0003g0094others(9): Show | 14 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.-97-3609_-97-3602d others(10): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117331981 | |||||
chr11:117331981
|
A | AATATATA others(3): Show |
4 | a0002c0001t0003g0097a0002c0001t0003g0363a0002c0001t0003g0364others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-97-3611_-97-3602d others(12): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117331981 | |||||
chr11:117331981
|
A | AATATATA others(5): Show |
1 | a0002c0001t0024g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-97-3613_-97-3602d others(14): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117331981 | |||||
chr11:117331981
|
AAT | A | 12 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(9): Show | 12 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.-97-3603_-97-3602d others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117331981 | |||||
chr11:117332004
|
T | A | 1 | a0002c0001t0003g0092 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-97-3601T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117332004 | ||||||
chr11:117332064
|
A | G | 12 | a0003c0003t0004g0034a0003c0003t0004g0035a0003c0003t0004g0132others(9): Show | 12 | HG00408.hp1 HG01433.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.-97-3541A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117332064 | ||||||
chr11:117332066
|
C | T | 6 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(3): Show | 6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-97-3539C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117332066 | ||||||
chr11:117332128
|
C | T | 1 | a0003c0003t0004g0131 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-97-3477C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117332128 | ||||||
chr11:117332332
|
T | G | 1 | a0002c0001t0003g0185 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-97-3273T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117332332 | ||||||
chr11:117332917
|
A | G | 91 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0042others(88): Show | 93 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.-97-2688A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117332917 | ||||||
chr11:117333000
|
A | C | 1 | a0003c0003t0004g0130 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-97-2605A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117333000 | ||||||
chr11:117333202
|
C | CAG | 290 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(287): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.-97-2403_-97-2402i others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117333202 | ||||||
chr11:117333216
|
T | C | 1 | a0006c0007t0006g0030 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-97-2389T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117333216 | ||||||
chr11:117333480
|
T | C | 1 | a0002c0001t0001g0090 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-97-2125T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117333480 | ||||||
chr11:117333742
|
C | T | 3 | a0002c0001t0003g0219a0002c0001t0003g0263a0002c0001t0003g0264 | 3 | NA18940.hp2 NA18950.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-97-1863C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117333742 | ||||||
chr11:117333941
|
G | A | 5 | a0003c0003t0004g0104a0003c0003t0004g0105a0003c0003t0004g0106others(2): Show | 5 | HG02698.hp2 HG03239.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.-97-1664G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117333941 | ||||||
chr11:117333972
|
G | A | 4 | a0003c0003t0004g0006a0003c0003t0004g0109a0003c0003t0004g0110others(1): Show | 5 | HG01928.hp2 HG01981.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-97-1633G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117333972 | ||||||
chr11:117334078
|
T | C | 1 | a0003c0003t0004g0098 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-97-1527T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117334078 | ||||||
chr11:117334228
|
T | G | 1 | a0003c0003t0004g0132 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-97-1377T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117334228 | ||||||
chr11:117334343
|
T | C | 1 | a0002c0001t0003g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-97-1262T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117334343 | ||||||
chr11:117334784
|
C | CA | 32 | a0001c0002t0001g0253a0001c0002t0002g0352a0001c0002t0002g0353others(29): Show | 32 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.-97-802dupA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117334784 | |||||
chr11:117334784
|
C | CAA | 175 | a0001c0002t0001g0037a0001c0002t0001g0252a0001c0002t0001g0306others(172): Show | 189 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(186): Show |
intron_variant | MODIFIER | c.-97-803_-97-802dup others(2): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117334784 | |||||
chr11:117334784
|
C | CAAA | 7 | a0001c0002t0001g0050a0001c0002t0002g0144a0001c0002t0002g0237others(4): Show | 7 | HG00544.hp2 HG01106.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.-97-804_-97-802dup others(3): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117334784 | |||||
chr11:117334784
|
CA | C | 8 | a0001c0002t0001g0042a0001c0002t0001g0071a0002c0001t0001g0090others(5): Show | 8 | HG01069.hp1 HG01168.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.-97-802delA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117334784 | |||||
chr11:117334827
|
A | G | 1 | a0004c0004t0001g0067 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-97-778A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117334827 | ||||||
chr11:117335050
|
T | C | 90 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0042others(87): Show | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-97-555T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117335050 | ||||||
chr11:117335128
|
G | T | 90 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0042others(87): Show | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-97-477G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117335128 | ||||||
chr11:117335145
|
C | T | 6 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(3): Show | 6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-97-460C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117335145 | ||||||
chr11:117335149
|
T | G | 1 | a0003c0003t0004g0111 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-97-456T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117335149 | ||||||
chr11:117335160
|
G | C | 4 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0042others(1): Show | 4 | HG02630.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-97-445G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117335160 | ||||||
chr11:117335579
|
C | CT | 23 | a0001c0005t0005g0250a0002c0001t0001g0090a0002c0001t0003g0002others(20): Show | 26 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(23): Show |
splice_region_variant&intron_variant | LOW | c.-97-8dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117335579 | |||||
chr11:117335712
|
C | T | 3 | a0004c0034t0007g0039a0008c0011t0007g0028a0024c0030t0021g0038 | 3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-22+32C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117335712 | ||||||
chr11:117335971
|
C | CT | 6 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(3): Show | 6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+292dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117335971 | |||||
chr11:117335988
|
C | T | 3 | a0011c0014t0013g0183a0011c0014t0013g0254a0026c0035t0013g0046 | 3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-22+308C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117335988 | ||||||
chr11:117336091
|
G | T | 9 | a0006c0007t0006g0029a0006c0007t0006g0030a0006c0007t0006g0265others(6): Show | 9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22+411G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336091 | ||||||
chr11:117336151
|
A | G | 1 | a0001c0002t0001g0326 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-22+471A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336151 | ||||||
chr11:117336212
|
CG | C | 3 | a0004c0034t0007g0039a0008c0011t0007g0028a0024c0030t0021g0038 | 3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-22+533delG | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336212 | ||||||
chr11:117336406
|
G | C | 21 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(18): Show | 21 | HG00323.hp1 HG00597.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-22+726G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336406 | ||||||
chr11:117336798
|
C | G | 1 | a0004c0004t0001g0315 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-22+1118C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336798 | ||||||
chr11:117336910
|
T | C | 90 | a0001c0002t0002g0145a0001c0002t0002g0235a0001c0002t0002g0238others(87): Show | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-22+1230T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336910 | ||||||
chr11:117336912
|
C | G | 90 | a0001c0002t0002g0145a0001c0002t0002g0235a0001c0002t0002g0238others(87): Show | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-22+1232C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336912 | ||||||
chr11:117336949
|
G | T | 77 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0003g0177others(74): Show | 83 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-22+1269G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336949 | ||||||
chr11:117336980
|
G | A | 5 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+1300G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336980 | ||||||
chr11:117336998
|
A | T | 1 | a0005c0006t0008g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-22+1318A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336998 | ||||||
chr11:117337226
|
T | A | 1 | a0002c0001t0003g0204 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-21-1340T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117337226 | ||||||
chr11:117337510
|
T | TAAAAAAA others(3): Show |
3 | a0003c0003t0004g0132a0003c0003t0005g0083a0006c0007t0006g0029 | 3 | HG02897.hp1 NA18988.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-21-1051_-21-1042d others(12): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | |||||
chr11:117337510
|
T | TAAAAAAA others(4): Show |
63 | a0002c0001t0001g0056a0003c0003t0002g0128a0003c0003t0004g0006others(60): Show | 65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.-21-1052_-21-1042d others(13): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | |||||
chr11:117337510
|
T | TAAAAAAA others(5): Show |
4 | a0003c0003t0004g0099a0005c0006t0007g0049a0005c0006t0007g0075others(1): Show | 4 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21-1053_-21-1042d others(14): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | |||||
chr11:117337510
|
T | TAAAAAAA others(6): Show |
1 | a0005c0006t0007g0048 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-21-1054_-21-1042d others(15): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | |||||
chr11:117337510
|
T | TAAAAAAA others(7): Show |
1 | a0005c0006t0007g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-21-1055_-21-1042d others(16): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | |||||
chr11:117337510
|
T | TAAAAAAA others(21): Show |
1 | a0016c0023t0006g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-21-1042_-21-1041i others(30): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | |||||
chr11:117337510
|
T | TAAAAAAA others(22): Show |
3 | a0006c0007t0006g0030a0006c0007t0006g0267a0010c0012t0006g0268 | 3 | HG03704.hp2 HG04199.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-21-1042_-21-1041i others(31): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | |||||
chr11:117337510
|
T | TAAAAAAA others(23): Show |
3 | a0006c0007t0006g0265a0006c0007t0006g0270a0010c0012t0006g0266 | 3 | HG00597.hp2 HG03710.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.-21-1042_-21-1041i others(32): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | |||||
chr11:117337510
|
T | TAAAAAAA others(24): Show |
1 | a0004c0009t0008g0023 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-21-1042_-21-1041i others(33): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | |||||
chr11:117337510
|
T | TAAAAAAA others(27): Show |
1 | a0006c0007t0006g0271 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-21-1042_-21-1041i others(36): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | |||||
chr11:117337510
|
T | TAAAAAAA others(30): Show |
1 | a0004c0009t0008g0026 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-21-1042_-21-1041i others(39): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | |||||
chr11:117337510
|
T | TAAAAAAA others(31): Show |
2 | a0004c0009t0008g0021a0004c0009t0008g0022 | 2 | HG01884.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-21-1042_-21-1041i others(40): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | |||||
chr11:117337554
|
G | A | 85 | a0002c0001t0001g0056a0003c0003t0002g0128a0003c0003t0004g0006others(82): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.-21-1012G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117337554 | ||||||
chr11:117337722
|
G | A | 1 | a0004c0004t0001g0310 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-21-844G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117337722 | ||||||
chr11:117337983
|
C | T | 1 | a0001c0002t0002g0351 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-21-583C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117337983 | ||||||
chr11:117338003
|
C | T | 1 | a0003c0003t0004g0098 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-21-563C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338003 | ||||||
chr11:117338027
|
C | T | 1 | a0001c0013t0005g0279 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-21-539C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338027 | ||||||
chr11:117338031
|
T | C | 85 | a0002c0001t0001g0056a0003c0003t0002g0128a0003c0003t0004g0006others(82): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.-21-535T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338031 | ||||||
chr11:117338122
|
G | A | 1 | a0002c0001t0003g0176 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-21-444G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338122 | ||||||
chr11:117338140
|
C | T | 1 | a0005c0006t0008g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-21-426C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338140 | ||||||
chr11:117338233
|
C | T | 74 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(71): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-21-333C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338233 | ||||||
chr11:117338297
|
G | A | 1 | a0001c0005t0005g0084 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-21-269G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338297 | ||||||
chr11:117338441
|
G | A | 1 | a0001c0002t0002g0339 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-21-125G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338441 | ||||||
chr11:117338449
|
C | T | 9 | a0006c0007t0006g0029a0006c0007t0006g0030a0006c0007t0006g0265others(6): Show | 9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21-117C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338449 | ||||||
chr11:117338552
|
C | T | 85 | a0002c0001t0001g0056a0003c0003t0002g0128a0003c0003t0004g0006others(82): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.-21-14C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338552 | ||||||
chr11:117338697
|
G | A | 1 | a0004c0004t0001g0289 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.82+29G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117338697 | ||||||
chr11:117338879
|
G | A | 5 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+211G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117338879 | ||||||
chr11:117338943
|
G | A | 1 | a0003c0003t0004g0104 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.82+275G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117338943 | ||||||
chr11:117339070
|
C | T | 2 | a0001c0002t0004g0361a0002c0001t0002g0324 | 2 | HG02132.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.82+402C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339070 | ||||||
chr11:117339076
|
C | T | 3 | a0004c0034t0007g0039a0008c0011t0007g0028a0024c0030t0021g0038 | 3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.82+408C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339076 | ||||||
chr11:117339132
|
G | C | 3 | a0011c0014t0013g0183a0011c0014t0013g0254a0026c0035t0013g0046 | 3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.82+464G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339132 | ||||||
chr11:117339266
|
G | T | 1 | a0001c0002t0002g0351 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.82+598G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339266 | ||||||
chr11:117339483
|
T | C | 6 | a0002c0001t0003g0010a0002c0001t0003g0097a0002c0001t0003g0255others(3): Show | 7 | HG02055.hp2 HG02723.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.82+815T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339483 | ||||||
chr11:117339511
|
CTTTGTTT | C | 17 | a0003c0003t0004g0035a0003c0003t0004g0108a0003c0003t0004g0110others(14): Show | 17 | HG00408.hp1 HG00597.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.82+854_82+860delGT others(5): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr11 | 117339511 | |||||
chr11:117339515
|
GTTTTTTG others(1): Show |
G | 65 | a0002c0001t0001g0056a0003c0003t0002g0128a0003c0003t0004g0006others(62): Show | 67 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.82+854_82+861delGT others(6): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr11 | 117339515 | |||||
chr11:117339520
|
TTG | T | 84 | a0001c0002t0001g0326a0001c0002t0002g0008a0001c0002t0002g0017others(81): Show | 90 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.82+854_82+855delGT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr11 | 117339520 | |||||
chr11:117339521
|
TG | T | 30 | a0001c0002t0002g0001a0001c0002t0002g0087a0001c0002t0002g0088others(27): Show | 33 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.82+854delG | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339521 | ||||||
chr11:117339522
|
G | T | 3 | a0001c0002t0002g0175a0001c0005t0005g0331a0007c0010t0002g0174 | 3 | HG01243.hp2 HG03453.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.82+854G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339522 | ||||||
chr11:117339522
|
GT | G | 99 | a0001c0002t0003g0177a0001c0005t0005g0146a0002c0001t0001g0004others(96): Show | 110 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.82+878delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr11 | 117339522 | |||||
chr11:117339522
|
GTT | G | 43 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(40): Show | 44 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.82+877_82+878delTT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr11 | 117339522 | |||||
chr11:117339525
|
T | G | 1 | a0001c0005t0005g0281 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.82+857T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339525 | ||||||
chr11:117339530
|
T | G | 1 | a0002c0001t0003g0012 | 2 | NA19062.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.82+862T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339530 | ||||||
chr11:117339531
|
T | G | 3 | a0001c0002t0001g0306a0004c0015t0003g0025a0026c0035t0013g0046 | 3 | HG00323.hp1 HG03225.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.82+863T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339531 | ||||||
chr11:117339622
|
G | A | 6 | a0004c0004t0001g0027a0004c0004t0001g0311a0004c0004t0001g0312others(3): Show | 6 | HG02155.hp1 NA18968.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.82+954G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339622 | ||||||
chr11:117339631
|
C | T | 11 | a0002c0001t0003g0066a0002c0001t0003g0092a0004c0004t0001g0003others(8): Show | 13 | NA18945.hp2 NA18954.hp1 NA18959.hp1 others(10): Show |
intron_variant | MODIFIER | c.82+963C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339631 | ||||||
chr11:117339991
|
G | A | 85 | a0002c0001t0001g0056a0003c0003t0002g0128a0003c0003t0004g0006others(82): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.82+1323G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339991 | ||||||
chr11:117340005
|
A | T | 1 | a0001c0002t0002g0339 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.82+1337A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117340005 | ||||||
chr11:117340070
|
G | A | 1 | a0001c0005t0005g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.82+1402G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117340070 | ||||||
chr11:117340172
|
C | T | 6 | a0002c0001t0003g0010a0002c0001t0003g0097a0002c0001t0003g0255others(3): Show | 7 | HG02055.hp2 HG02723.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.82+1504C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117340172 | ||||||
chr11:117340185
|
T | C | 85 | a0002c0001t0001g0056a0003c0003t0002g0128a0003c0003t0004g0006others(82): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.82+1517T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117340185 | ||||||
chr11:117340268
|
C | T | 5 | a0001c0002t0001g0326a0001c0002t0002g0320a0001c0002t0002g0321others(2): Show | 5 | NA18941.hp1 NA18970.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+1600C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117340268 | ||||||
chr11:117340482
|
G | A | 3 | a0008c0011t0012g0080a0008c0011t0012g0081a0025c0029t0012g0079 | 3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.82+1814G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117340482 | ||||||
chr11:117340524
|
G | T | 81 | a0002c0001t0001g0056a0003c0003t0002g0128a0003c0003t0004g0006others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.82+1856G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117340524 | ||||||
chr11:117340831
|
TTC | T | 3 | a0004c0034t0007g0039a0008c0011t0007g0028a0024c0030t0021g0038 | 3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.82+2165_82+2166del others(2): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr11 | 117340831 | |||||
chr11:117341078
|
C | T | 1 | a0023c0032t0020g0193 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.82+2410C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117341078 | ||||||
chr11:117341207
|
A | G | 1 | a0010c0012t0006g0268 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.82+2539A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117341207 | ||||||
chr11:117341370
|
A | G | 1 | a0009c0021t0019g0082 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.82+2702A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117341370 | ||||||
chr11:117341415
|
C | G | 2 | a0011c0014t0013g0183a0011c0014t0013g0254 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.82+2747C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117341415 | ||||||
chr11:117341437
|
TTTG | T | 39 | a0001c0005t0005g0009a0001c0005t0005g0032a0001c0005t0005g0033others(36): Show | 40 | HG00323.hp1 HG00423.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.83-2723_83-2721del others(3): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr11 | 117341437 | |||||
chr11:117341455
|
T | G | 1 | a0001c0005t0005g0250 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.83-2711T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117341455 | ||||||
chr11:117341557
|
C | T | 5 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.83-2609C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117341557 | ||||||
chr11:117341579
|
G | A | 1 | a0001c0002t0002g0147 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.83-2587G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117341579 | ||||||
chr11:117341621
|
G | T | 89 | a0002c0001t0001g0056a0002c0001t0003g0220a0002c0001t0003g0221others(86): Show | 91 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.83-2545G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117341621 | ||||||
chr11:117341924
|
T | C | 86 | a0002c0001t0001g0056a0003c0003t0002g0128a0003c0003t0004g0006others(83): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.83-2242T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117341924 | ||||||
chr11:117342176
|
C | T | 86 | a0002c0001t0001g0056a0003c0003t0002g0128a0003c0003t0004g0006others(83): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.83-1990C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117342176 | ||||||
chr11:117342192
|
A | G | 67 | a0002c0001t0001g0056a0003c0003t0002g0128a0003c0003t0004g0006others(64): Show | 69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.83-1974A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117342192 | ||||||
chr11:117342443
|
C | T | 1 | a0007c0010t0002g0181 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.83-1723C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117342443 | ||||||
chr11:117342444
|
G | A | 86 | a0002c0001t0001g0056a0003c0003t0002g0128a0003c0003t0004g0006others(83): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.83-1722G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117342444 | ||||||
chr11:117342473
|
G | A | 36 | a0004c0004t0001g0015a0004c0004t0001g0016a0004c0004t0001g0027others(33): Show | 37 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.83-1693G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117342473 | ||||||
chr11:117342754
|
G | A | 4 | a0001c0002t0002g0148a0001c0002t0002g0149a0001c0002t0002g0164others(1): Show | 4 | HG00609.hp1 NA18940.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-1412G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117342754 | ||||||
chr11:117343131
|
A | G | 79 | a0001c0002t0001g0326a0001c0002t0002g0001a0001c0002t0002g0008others(76): Show | 87 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.83-1035A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117343131 | ||||||
chr11:117343177
|
A | G | 43 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(40): Show | 44 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.83-989A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117343177 | ||||||
chr11:117343242
|
G | T | 1 | a0003c0003t0011g0232 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.83-924G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117343242 | ||||||
chr11:117343375
|
G | A | 86 | a0002c0001t0001g0056a0003c0003t0002g0128a0003c0003t0004g0006others(83): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.83-791G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117343375 | ||||||
chr11:117343629
|
C | CT | 84 | a0001c0002t0001g0334a0001c0002t0002g0247a0001c0002t0002g0248others(81): Show | 86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.83-519dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr11 | 117343629 | |||||
chr11:117343629
|
C | CTT | 7 | a0003c0003t0002g0128a0003c0003t0004g0107a0003c0003t0004g0110others(4): Show | 7 | HG00597.hp2 HG00741.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.83-520_83-519dupTT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr11 | 117343629 | |||||
chr11:117343743
|
G | C | 1 | a0009c0021t0019g0082 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.83-423G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117343743 | ||||||
chr11:117343864
|
G | C | 262 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(259): Show | 274 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.83-302G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117343864 | ||||||
chr11:117343966
|
T | C | 2 | a0001c0002t0001g0317a0001c0002t0001g0334 | 2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.83-200T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117343966 | ||||||
chr11:117344032
|
A | G | 2 | a0001c0002t0001g0050a0001c0002t0001g0253 | 2 | HG01167.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.83-134A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117344032 | ||||||
chr11:117344290
|
G | T | 3 | a0005c0006t0008g0045a0009c0020t0014g0327a0013c0018t0014g0269 | 3 | HG02559.hp1 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.194+13G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344290 | ||||||
chr11:117344297
|
G | A | 1 | a0009c0021t0019g0082 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.194+20G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344297 | ||||||
chr11:117344301
|
A | G | 3 | a0004c0034t0007g0039a0008c0011t0007g0028a0024c0030t0021g0038 | 3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.194+24A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344301 | ||||||
chr11:117344352
|
G | A | 5 | a0001c0002t0002g0017a0001c0002t0002g0350a0001c0002t0002g0352others(2): Show | 6 | HG01952.hp1 HG01975.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.194+75G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344352 | ||||||
chr11:117344389
|
A | G | 1 | a0002c0001t0001g0059 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.194+112A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344389 | ||||||
chr11:117344656
|
G | A | 1 | a0005c0006t0008g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.194+379G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344656 | ||||||
chr11:117344712
|
A | G | 1 | a0001c0002t0001g0252 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.194+435A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344712 | ||||||
chr11:117344764
|
T | C | 2 | a0002c0001t0003g0190a0023c0032t0020g0193 | 2 | HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.194+487T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344764 | ||||||
chr11:117344889
|
C | T | 37 | a0001c0005t0005g0009a0001c0005t0005g0032a0001c0005t0005g0033others(34): Show | 38 | HG00423.hp2 HG01099.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.194+612C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344889 | ||||||
chr11:117344974
|
T | C | 3 | a0011c0014t0013g0183a0011c0014t0013g0254a0026c0035t0013g0046 | 3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.194+697T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344974 | ||||||
chr11:117345029
|
G | A | 1 | a0002c0001t0003g0201 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.194+752G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345029 | ||||||
chr11:117345297
|
C | T | 3 | a0008c0011t0012g0080a0008c0011t0012g0081a0025c0029t0012g0079 | 3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.194+1020C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345297 | ||||||
chr11:117345497
|
T | G | 88 | a0002c0001t0001g0056a0003c0003t0002g0128a0003c0003t0004g0006others(85): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.194+1220T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345497 | ||||||
chr11:117345621
|
G | A | 1 | a0004c0004t0001g0311 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.194+1344G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345621 | ||||||
chr11:117345635
|
TG | T | 78 | a0001c0002t0001g0326a0001c0002t0002g0001a0001c0002t0002g0008others(75): Show | 86 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.194+1359delG | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345635 | ||||||
chr11:117345712
|
G | A | 1 | a0019c0025t0001g0303 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.194+1435G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345712 | ||||||
chr11:117345719
|
T | C | 1 | a0002c0001t0003g0195 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.194+1442T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345719 | ||||||
chr11:117345784
|
G | T | 1 | a0002c0001t0002g0324 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.194+1507G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345784 | ||||||
chr11:117345791
|
G | C | 3 | a0011c0014t0013g0183a0011c0014t0013g0254a0026c0035t0013g0046 | 3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.194+1514G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345791 | ||||||
chr11:117345883
|
C | T | 66 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(63): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.194+1606C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345883 | ||||||
chr11:117345887
|
A | T | 55 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(52): Show | 56 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.194+1610A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345887 | ||||||
chr11:117345912
|
C | T | 4 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(1): Show | 4 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.194+1635C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345912 | ||||||
chr11:117345967
|
G | T | 5 | a0002c0001t0009g0184a0002c0001t0009g0192a0002c0001t0009g0256others(2): Show | 5 | HG01074.hp1 HG01243.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.194+1690G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345967 | ||||||
chr11:117346001
|
C | A | 1 | a0009c0021t0019g0082 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.194+1724C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117346001 | ||||||
chr11:117346266
|
A | G | 1 | a0002c0001t0003g0096 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.194+1989A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117346266 | ||||||
chr11:117346391
|
T | C | 1 | a0007c0010t0002g0181 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.194+2114T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117346391 | ||||||
chr11:117346455
|
C | T | 1 | a0003c0003t0004g0132 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.194+2178C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117346455 | ||||||
chr11:117346456
|
G | A | 12 | a0002c0001t0003g0002a0002c0001t0003g0185a0002c0001t0003g0186others(9): Show | 15 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.194+2179G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117346456 | ||||||
chr11:117346558
|
A | G | 1 | a0005c0006t0008g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.194+2281A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117346558 | ||||||
chr11:117346675
|
G | T | 165 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(162): Show | 175 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.194+2398G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117346675 | ||||||
chr11:117346684
|
C | T | 1 | a0009c0021t0019g0082 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.194+2407C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117346684 | ||||||
chr11:117346817
|
C | G | 36 | a0001c0002t0001g0326a0001c0002t0002g0017a0001c0002t0002g0018others(33): Show | 40 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.194+2540C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117346817 | ||||||
chr11:117347160
|
TTTATTTG others(27): Show |
T | 1 | a0003c0003t0004g0110 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.194+2884_194+2917d others(36): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117347160 | ||||||
chr11:117347508
|
C | T | 1 | a0003c0003t0004g0127 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.194+3231C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117347508 | ||||||
chr11:117347571
|
G | A | 3 | a0002c0001t0001g0013a0002c0001t0001g0282a0002c0001t0001g0283 | 4 | NA18955.hp1 NA18957.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.194+3294G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117347571 | ||||||
chr11:117347590
|
AT | A | 5 | a0001c0002t0001g0050a0001c0002t0001g0252a0001c0002t0001g0253others(2): Show | 5 | HG01069.hp2 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.194+3314delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117347590 | ||||||
chr11:117347658
|
C | T | 1 | a0001c0002t0002g0323 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.194+3381C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117347658 | ||||||
chr11:117347710
|
C | CA | 8 | a0001c0002t0001g0050a0001c0002t0001g0252a0001c0002t0001g0253others(5): Show | 8 | HG01069.hp2 HG01167.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.194+3447dupA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr11 | 117347710 | |||||
chr11:117347744
|
T | C | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.194+3467T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117347744 | ||||||
chr11:117347955
|
T | TTTG | 3 | a0006c0007t0006g0029a0006c0007t0006g0030a0016c0023t0006g0031 | 3 | HG03834.hp2 HG04199.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.194+3705_194+3707d others(5): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr11 | 117347955 | |||||
chr11:117348046
|
G | A | 37 | a0001c0005t0005g0009a0001c0005t0005g0032a0001c0005t0005g0033others(34): Show | 38 | HG00423.hp2 HG01099.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.195-3744G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117348046 | ||||||
chr11:117348274
|
G | C | 1 | a0025c0029t0012g0079 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.195-3516G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117348274 | ||||||
chr11:117348364
|
C | T | 1 | a0003c0003t0004g0111 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.195-3426C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117348364 | ||||||
chr11:117348388
|
G | A | 1 | a0005c0006t0008g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.195-3402G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117348388 | ||||||
chr11:117348589
|
G | C | 87 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(84): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.195-3201G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117348589 | ||||||
chr11:117348672
|
T | C | 3 | a0004c0034t0007g0039a0008c0011t0007g0028a0024c0030t0021g0038 | 3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.195-3118T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117348672 | ||||||
chr11:117348756
|
C | G | 3 | a0001c0005t0005g0275a0001c0005t0005g0276a0001c0005t0005g0277 | 3 | HG01168.hp2 HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.195-3034C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117348756 | ||||||
chr11:117349054
|
G | A | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.195-2736G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117349054 | ||||||
chr11:117349085
|
C | T | 6 | a0006c0007t0006g0265a0006c0007t0006g0267a0006c0007t0006g0270others(3): Show | 6 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.195-2705C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117349085 | ||||||
chr11:117349096
|
C | T | 1 | a0002c0001t0001g0053 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.195-2694C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117349096 | ||||||
chr11:117349245
|
A | G | 118 | a0001c0002t0001g0326a0001c0002t0002g0001a0001c0002t0002g0008others(115): Show | 127 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.195-2545A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117349245 | ||||||
chr11:117349250
|
C | T | 1 | a0002c0001t0009g0184 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.195-2540C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117349250 | ||||||
chr11:117349430
|
G | T | 3 | a0001c0005t0005g0275a0001c0005t0005g0276a0001c0005t0005g0277 | 3 | HG01168.hp2 HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.195-2360G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117349430 | ||||||
chr11:117349608
|
C | T | 5 | a0001c0002t0001g0050a0001c0002t0001g0252a0001c0002t0001g0253others(2): Show | 5 | HG01069.hp2 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.195-2182C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117349608 | ||||||
chr11:117349713
|
A | C | 1 | a0003c0003t0004g0126 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.195-2077A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117349713 | ||||||
chr11:117349884
|
C | T | 9 | a0006c0007t0006g0029a0006c0007t0006g0030a0006c0007t0006g0265others(6): Show | 9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.195-1906C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117349884 | ||||||
chr11:117350009
|
G | A | 3 | a0001c0002t0002g0320a0001c0002t0002g0321a0001c0002t0002g0323 | 3 | NA18941.hp1 NA19010.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.195-1781G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350009 | ||||||
chr11:117350098
|
G | A | 1 | a0009c0021t0019g0082 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.195-1692G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350098 | ||||||
chr11:117350198
|
C | T | 7 | a0001c0005t0005g0009a0001c0005t0005g0086a0001c0005t0005g0146others(4): Show | 8 | NA18957.hp2 NA18970.hp1 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.195-1592C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350198 | ||||||
chr11:117350208
|
CT | C | 66 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(63): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.195-1570delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr11 | 117350208 | |||||
chr11:117350277
|
A | G | 3 | a0004c0034t0007g0039a0008c0011t0007g0028a0024c0030t0021g0038 | 3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.195-1513A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350277 | ||||||
chr11:117350412
|
C | T | 1 | a0004c0008t0001g0301 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.195-1378C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350412 | ||||||
chr11:117350454
|
T | G | 283 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(280): Show | 299 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.195-1336T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350454 | ||||||
chr11:117350508
|
A | T | 1 | a0001c0026t0002g0154 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.195-1282A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350508 | ||||||
chr11:117350667
|
G | C | 9 | a0006c0007t0006g0029a0006c0007t0006g0030a0006c0007t0006g0265others(6): Show | 9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.195-1123G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350667 | ||||||
chr11:117350754
|
A | G | 3 | a0011c0014t0013g0183a0011c0014t0013g0254a0026c0035t0013g0046 | 3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.195-1036A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350754 | ||||||
chr11:117350852
|
A | G | 4 | a0003c0003t0005g0083a0003c0003t0005g0116a0003c0003t0005g0117others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.195-938A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350852 | ||||||
chr11:117351034
|
T | G | 1 | a0004c0004t0001g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.195-756T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117351034 | ||||||
chr11:117351129
|
T | G | 1 | a0001c0005t0005g0275 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.195-661T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117351129 | ||||||
chr11:117351146
|
C | T | 2 | a0002c0001t0001g0004a0002c0001t0001g0056 | 3 | HG01106.hp1 NA20752.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.195-644C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117351146 | ||||||
chr11:117351221
|
G | C | 1 | a0002c0001t0003g0220 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.195-569G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117351221 | ||||||
chr11:117351259
|
G | A | 5 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.195-531G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117351259 | ||||||
chr11:117351423
|
C | T | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.195-367C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117351423 | ||||||
chr11:117351434
|
C | T | 1 | a0011c0014t0013g0254 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.195-356C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117351434 | ||||||
chr11:117351540
|
T | C | 40 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0004g0069others(37): Show | 46 | HG00099.hp1 HG00140.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.195-250T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117351540 | ||||||
chr11:117352113
|
G | A | 14 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(11): Show | 14 | HG00597.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.393+125G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352113 | ||||||
chr11:117352226
|
G | T | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+238G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352226 | ||||||
chr11:117352290
|
C | T | 1 | a0002c0001t0003g0215 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.393+302C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352290 | ||||||
chr11:117352481
|
G | C | 8 | a0003c0003t0004g0098a0003c0003t0004g0100a0003c0003t0004g0112others(5): Show | 8 | HG02257.hp1 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.393+493G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352481 | ||||||
chr11:117352481
|
GTTCAAGA | G | 3 | a0004c0034t0007g0039a0008c0011t0007g0028a0024c0030t0021g0038 | 3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.393+496_393+502del others(7): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117352481 | |||||
chr11:117352517
|
A | G | 3 | a0005c0006t0008g0045a0009c0020t0014g0327a0013c0018t0014g0269 | 3 | HG02559.hp1 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.393+529A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352517 | ||||||
chr11:117352735
|
C | T | 1 | a0008c0011t0007g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.393+747C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352735 | ||||||
chr11:117352743
|
C | T | 1 | a0008c0011t0007g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.393+755C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352743 | ||||||
chr11:117352825
|
G | C | 1 | a0017c0024t0005g0141 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.393+837G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352825 | ||||||
chr11:117352834
|
G | A | 1 | a0004c0004t0001g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.393+846G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352834 | ||||||
chr11:117352844
|
C | T | 6 | a0006c0007t0006g0265a0006c0007t0006g0267a0006c0007t0006g0270others(3): Show | 6 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+856C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352844 | ||||||
chr11:117352972
|
T | A | 1 | a0002c0001t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.393+984T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352972 | ||||||
chr11:117352976
|
T | C | 362 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(359): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.393+988T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352976 | ||||||
chr11:117353243
|
C | T | 1 | a0003c0003t0004g0226 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.393+1255C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117353243 | ||||||
chr11:117353290
|
C | T | 14 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(11): Show | 14 | HG00597.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.393+1302C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117353290 | ||||||
chr11:117353306
|
C | T | 1 | a0024c0030t0021g0038 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.393+1318C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117353306 | ||||||
chr11:117353434
|
T | C | 5 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+1446T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117353434 | ||||||
chr11:117353644
|
G | A | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+1656G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117353644 | ||||||
chr11:117353785
|
G | A | 1 | a0002c0001t0001g0057 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+1797G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117353785 | ||||||
chr11:117353997
|
TCTTCTC | T | 79 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(76): Show | 81 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.393+2015_393+2020d others(8): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117353997 | |||||
chr11:117354003
|
C | CCTT | 165 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(162): Show | 178 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.393+2034_393+2036d others(5): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117354003 | |||||
chr11:117354003
|
C | T | 1 | a0006c0007t0006g0267 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.393+2015C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354003 | ||||||
chr11:117354072
|
A | G | 4 | a0003c0003t0004g0006a0003c0003t0004g0109a0003c0003t0004g0110others(1): Show | 5 | HG01928.hp2 HG01981.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+2084A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354072 | ||||||
chr11:117354102
|
C | T | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+2114C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354102 | ||||||
chr11:117354127
|
G | A | 1 | a0005c0006t0008g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.393+2139G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354127 | ||||||
chr11:117354136
|
C | T | 3 | a0004c0034t0007g0039a0008c0011t0007g0028a0024c0030t0021g0038 | 3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.393+2148C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354136 | ||||||
chr11:117354162
|
G | A | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+2174G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354162 | ||||||
chr11:117354171
|
C | T | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+2183C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354171 | ||||||
chr11:117354178
|
G | A | 3 | a0008c0011t0012g0080a0008c0011t0012g0081a0025c0029t0012g0079 | 3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.393+2190G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354178 | ||||||
chr11:117354204
|
C | T | 5 | a0001c0005t0005g0329a0001c0005t0005g0331a0001c0005t0005g0355others(2): Show | 5 | HG01109.hp2 HG01123.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+2216C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354204 | ||||||
chr11:117354218
|
A | G | 4 | a0002c0001t0001g0004a0002c0001t0001g0056a0002c0001t0001g0059others(1): Show | 5 | HG00099.hp1 HG01106.hp1 NA20129.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+2230A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354218 | ||||||
chr11:117354229
|
G | T | 1 | a0009c0021t0019g0082 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.393+2241G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354229 | ||||||
chr11:117354268
|
G | A | 1 | a0001c0005t0005g0085 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.393+2280G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354268 | ||||||
chr11:117354317
|
T | C | 243 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(240): Show | 258 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.393+2329T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354317 | ||||||
chr11:117354418
|
G | A | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+2430G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354418 | ||||||
chr11:117354496
|
C | G | 1 | a0004c0004t0001g0300 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.393+2508C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354496 | ||||||
chr11:117354606
|
C | A | 1 | a0002c0001t0001g0060 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.393+2618C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354606 | ||||||
chr11:117354677
|
T | G | 1 | a0001c0002t0002g0350 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.393+2689T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354677 | ||||||
chr11:117354725
|
G | T | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+2737G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354725 | ||||||
chr11:117354739
|
T | A | 66 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(63): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.393+2751T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354739 | ||||||
chr11:117354751
|
T | A | 82 | a0001c0002t0004g0069a0003c0003t0002g0128a0003c0003t0004g0006others(79): Show | 84 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.393+2763T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354751 | ||||||
chr11:117354766
|
T | TTTTA | 7 | a0001c0002t0002g0036a0001c0002t0002g0340a0001c0002t0002g0341others(4): Show | 7 | HG02280.hp2 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.393+2805_393+2808d others(6): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117354766 | |||||
chr11:117354766
|
T | TTTTATTT others(1): Show |
4 | a0001c0002t0002g0020a0001c0002t0002g0339a0001c0002t0002g0360others(1): Show | 5 | HG00558.hp1 HG00621.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+2801_393+2808d others(10): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117354766 | |||||
chr11:117354766
|
TTTTA | T | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+2805_393+2808d others(6): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117354766 | |||||
chr11:117354900
|
C | T | 1 | a0002c0001t0001g0091 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.393+2912C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354900 | ||||||
chr11:117355101
|
G | T | 5 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+3113G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117355101 | ||||||
chr11:117355266
|
C | T | 36 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0044others(33): Show | 40 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.393+3278C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117355266 | ||||||
chr11:117355325
|
A | G | 4 | a0001c0002t0002g0148a0001c0002t0002g0149a0001c0002t0002g0164others(1): Show | 4 | HG00609.hp1 NA18940.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+3337A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117355325 | ||||||
chr11:117355529
|
A | C | 4 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0042others(1): Show | 4 | HG02630.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+3541A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117355529 | ||||||
chr11:117355546
|
A | G | 2 | a0011c0014t0013g0183a0011c0014t0013g0254 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.393+3558A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117355546 | ||||||
chr11:117355677
|
G | A | 3 | a0011c0014t0013g0183a0011c0014t0013g0254a0026c0035t0013g0046 | 3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.393+3689G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117355677 | ||||||
chr11:117355814
|
G | A | 1 | a0005c0006t0007g0076 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.393+3826G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117355814 | ||||||
chr11:117355900
|
T | C | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+3912T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117355900 | ||||||
chr11:117355903
|
C | T | 23 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(20): Show | 24 | HG00408.hp1 HG01433.hp2 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.393+3915C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117355903 | ||||||
chr11:117355999
|
G | GAGCAGCA others(2): Show |
80 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(77): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.393+4025_393+4033d others(11): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117355999 | |||||
chr11:117355999
|
G | GAGCAGCA others(11): Show |
1 | a0003c0003t0004g0230 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.393+4016_393+4033d others(20): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117355999 | |||||
chr11:117356049
|
C | G | 1 | a0026c0035t0013g0046 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.393+4061C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356049 | ||||||
chr11:117356057
|
C | A | 5 | a0001c0002t0001g0050a0001c0002t0001g0252a0001c0002t0001g0253others(2): Show | 5 | HG01069.hp2 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+4069C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356057 | ||||||
chr11:117356133
|
C | T | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+4145C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356133 | ||||||
chr11:117356225
|
T | A | 5 | a0001c0002t0001g0050a0001c0002t0001g0252a0001c0002t0001g0253others(2): Show | 5 | HG01069.hp2 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+4237T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356225 | ||||||
chr11:117356346
|
C | T | 2 | a0001c0002t0002g0019a0001c0002t0002g0353 | 3 | NA18944.hp1 NA19007.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.393+4358C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356346 | ||||||
chr11:117356657
|
G | C | 1 | a0001c0026t0002g0154 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.393+4669G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356657 | ||||||
chr11:117356673
|
G | A | 1 | a0004c0004t0001g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.393+4685G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356673 | ||||||
chr11:117356765
|
C | T | 3 | a0005c0006t0008g0045a0009c0020t0014g0327a0013c0018t0014g0269 | 3 | HG02559.hp1 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.393+4777C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356765 | ||||||
chr11:117356803
|
T | C | 194 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0002g0150others(191): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.393+4815T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356803 | ||||||
chr11:117356869
|
A | T | 4 | a0004c0008t0001g0297a0004c0008t0001g0298a0004c0008t0001g0299others(1): Show | 4 | HG01361.hp2 HG01433.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+4881A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356869 | ||||||
chr11:117356970
|
G | A | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-4865G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356970 | ||||||
chr11:117356978
|
T | C | 66 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(63): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.394-4857T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356978 | ||||||
chr11:117356994
|
C | G | 2 | a0011c0014t0013g0183a0011c0014t0013g0254 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.394-4841C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356994 | ||||||
chr11:117357002
|
A | G | 1 | a0004c0004t0001g0093 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.394-4833A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357002 | ||||||
chr11:117357049
|
T | A | 3 | a0001c0002t0002g0020a0001c0002t0002g0339a0001c0002t0002g0360 | 4 | HG00558.hp1 HG00621.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-4786T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357049 | ||||||
chr11:117357274
|
T | A | 26 | a0001c0002t0003g0177a0002c0001t0003g0066a0002c0001t0003g0092others(23): Show | 26 | HG00408.hp2 HG02040.hp1 NA18612.hp2 others(23): Show |
intron_variant | MODIFIER | c.394-4561T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357274 | ||||||
chr11:117357356
|
GCCTTGGC others(5): Show |
G | 6 | a0006c0007t0006g0265a0006c0007t0006g0267a0006c0007t0006g0270others(3): Show | 6 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.394-4477_394-4466d others(14): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117357356 | |||||
chr11:117357423
|
C | CT | 79 | a0001c0002t0001g0326a0001c0002t0002g0001a0001c0002t0002g0008others(76): Show | 87 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.394-4392dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117357423 | |||||
chr11:117357423
|
CTTTTTTT others(2): Show |
C | 63 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(60): Show | 65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.394-4400_394-4392d others(11): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117357423 | |||||
chr11:117357423
|
CTTTTTTT others(3): Show |
C | 18 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(15): Show | 18 | HG00597.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.394-4401_394-4392d others(12): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117357423 | |||||
chr11:117357579
|
A | G | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-4256A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357579 | ||||||
chr11:117357640
|
T | A | 1 | a0001c0002t0002g0314 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.394-4195T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357640 | ||||||
chr11:117357644
|
A | T | 5 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-4191A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357644 | ||||||
chr11:117357659
|
T | C | 4 | a0003c0003t0005g0083a0003c0003t0005g0116a0003c0003t0005g0117others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-4176T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357659 | ||||||
chr11:117357803
|
A | G | 43 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(40): Show | 44 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.394-4032A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357803 | ||||||
chr11:117357948
|
G | A | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-3887G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357948 | ||||||
chr11:117357977
|
A | G | 1 | a0001c0002t0002g0149 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.394-3858A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357977 | ||||||
chr11:117357993
|
A | G | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-3842A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357993 | ||||||
chr11:117358133
|
A | G | 25 | a0001c0002t0001g0050a0001c0002t0001g0252a0001c0002t0001g0253others(22): Show | 29 | HG01069.hp2 HG01167.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.394-3702A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117358133 | ||||||
chr11:117358176
|
G | A | 327 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(324): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.394-3659G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117358176 | ||||||
chr11:117358402
|
A | AAT | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-3433_394-3432i others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117358402 | ||||||
chr11:117358540
|
C | CT | 20 | a0002c0001t0003g0012a0002c0001t0003g0094a0002c0001t0003g0095others(17): Show | 21 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.394-3277dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117358540 | |||||
chr11:117358540
|
C | CTT | 73 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(70): Show | 75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.394-3278_394-3277d others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117358540 | |||||
chr11:117358540
|
CT | C | 6 | a0001c0002t0002g0337a0001c0005t0005g0276a0002c0001t0001g0054others(3): Show | 6 | HG01074.hp1 HG01168.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-3277delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117358540 | |||||
chr11:117358604
|
T | C | 6 | a0004c0004t0001g0003a0004c0004t0001g0047a0004c0004t0001g0064others(3): Show | 7 | NA18959.hp1 NA18989.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-3231T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117358604 | ||||||
chr11:117358672
|
A | G | 3 | a0002c0001t0001g0013a0002c0001t0001g0282a0002c0001t0001g0283 | 4 | NA18955.hp1 NA18957.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-3163A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117358672 | ||||||
chr11:117358798
|
G | A | 3 | a0007c0010t0002g0167a0007c0010t0002g0168a0007c0010t0002g0174 | 3 | HG01074.hp2 HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.394-3037G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117358798 | ||||||
chr11:117358833
|
C | A | 1 | a0002c0001t0001g0061 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.394-3002C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117358833 | ||||||
chr11:117358948
|
C | CT | 86 | a0001c0005t0005g0163a0002c0001t0003g0191a0003c0003t0002g0128others(83): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.394-2873dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117358948 | |||||
chr11:117359031
|
A | G | 2 | a0001c0002t0001g0317a0001c0002t0001g0334 | 2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.394-2804A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117359031 | ||||||
chr11:117359117
|
G | T | 79 | a0001c0002t0001g0326a0001c0002t0002g0001a0001c0002t0002g0008others(76): Show | 87 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.394-2718G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117359117 | ||||||
chr11:117359175
|
C | T | 66 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(63): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.394-2660C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117359175 | ||||||
chr11:117359186
|
C | T | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-2649C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117359186 | ||||||
chr11:117359235
|
C | G | 2 | a0002c0001t0003g0134a0002c0001t0003g0135 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.394-2600C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117359235 | ||||||
chr11:117359595
|
C | T | 1 | a0001c0026t0002g0154 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.394-2240C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117359595 | ||||||
chr11:117359882
|
A | G | 1 | a0001c0002t0002g0088 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.394-1953A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117359882 | ||||||
chr11:117360150
|
C | G | 1 | a0009c0021t0019g0082 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.394-1685C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117360150 | ||||||
chr11:117360341
|
T | A | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-1494T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117360341 | ||||||
chr11:117360459
|
C | T | 2 | a0002c0001t0001g0013a0002c0001t0001g0283 | 3 | NA18957.hp1 NA18975.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.394-1376C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117360459 | ||||||
chr11:117360475
|
G | T | 1 | a0026c0035t0013g0046 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.394-1360G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117360475 | ||||||
chr11:117360703
|
G | A | 5 | a0001c0002t0001g0040a0001c0002t0001g0042a0001c0002t0001g0043others(2): Show | 5 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-1132G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117360703 | ||||||
chr11:117360895
|
G | T | 66 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(63): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.394-940G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117360895 | ||||||
chr11:117360936
|
C | CT | 109 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(106): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.394-883dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117360936 | |||||
chr11:117360961
|
G | T | 1 | a0001c0002t0002g0323 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.394-874G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117360961 | ||||||
chr11:117361027
|
C | T | 1 | a0003c0003t0004g0230 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.394-808C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361027 | ||||||
chr11:117361124
|
A | G | 2 | a0002c0001t0003g0178a0002c0001t0003g0179 | 2 | NA18967.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.394-711A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361124 | ||||||
chr11:117361233
|
C | CT | 78 | a0001c0002t0001g0050a0001c0002t0002g0018a0001c0002t0002g0088others(75): Show | 79 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.394-576dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117361233 | |||||
chr11:117361233
|
C | CTT | 8 | a0002c0001t0003g0195a0002c0001t0003g0258a0003c0003t0004g0120others(5): Show | 8 | HG00423.hp1 HG01978.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-577_394-576dup others(2): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117361233 | |||||
chr11:117361233
|
CT | C | 13 | a0001c0002t0001g0253a0001c0002t0002g0044a0001c0002t0002g0322others(10): Show | 13 | HG01167.hp2 HG01884.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.394-576delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117361233 | |||||
chr11:117361233
|
CTTTTTTT others(2): Show |
C | 4 | a0002c0001t0003g0002a0002c0001t0003g0185a0002c0001t0003g0194others(1): Show | 7 | HG00621.hp2 NA18945.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-584_394-576del others(9): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117361233 | |||||
chr11:117361309
|
C | T | 1 | a0002c0001t0003g0255 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.394-526C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361309 | ||||||
chr11:117361401
|
C | T | 1 | a0001c0005t0005g0162 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.394-434C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361401 | ||||||
chr11:117361440
|
C | G | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-395C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361440 | ||||||
chr11:117361484
|
C | G | 2 | a0003c0003t0005g0007a0003c0022t0005g0227 | 3 | HG01261.hp2 HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.394-351C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361484 | ||||||
chr11:117361517
|
G | A | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-318G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361517 | ||||||
chr11:117361544
|
A | G | 66 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(63): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.394-291A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361544 | ||||||
chr11:117361566
|
A | G | 1 | a0013c0018t0014g0269 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.394-269A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361566 | ||||||
chr11:117361675
|
A | G | 63 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(60): Show | 65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.394-160A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361675 | ||||||
chr11:117361776
|
C | T | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-59C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361776 | ||||||
chr11:117362087
|
A | G | 3 | a0008c0011t0012g0080a0008c0011t0012g0081a0025c0029t0012g0079 | 3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.552+94A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 6/32 | chr11 | 117362087 | ||||||
chr11:117362238
|
A | G | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.553-166A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 6/32 | chr11 | 117362238 | ||||||
chr11:117362316
|
T | C | 1 | a0003c0003t0004g0230 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.553-88T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 6/32 | chr11 | 117362316 | ||||||
chr11:117362332
|
G | A | 2 | a0004c0004t0001g0290a0004c0004t0001g0291 | 2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.553-72G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 6/32 | chr11 | 117362332 | ||||||
chr11:117362393
|
C | T | 2 | a0002c0001t0003g0214a0002c0001t0003g0218 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.553-11C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 6/32 | chr11 | 117362393 | ||||||
chr11:117362662
|
G | A | 1 | a0001c0002t0002g0362 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.687+124G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 7/32 | chr11 | 117362662 | ||||||
chr11:117362711
|
C | T | 76 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(73): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.687+173C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 7/32 | chr11 | 117362711 | ||||||
chr11:117362723
|
CT | C | 82 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(79): Show | 84 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.687+194delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr11 | 117362723 | |||||
chr11:117362849
|
A | G | 2 | a0003c0003t0005g0309a0003c0003t0005g0328 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.687+311A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 7/32 | chr11 | 117362849 | ||||||
chr11:117362920
|
C | T | 1 | a0004c0009t0008g0026 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.687+382C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 7/32 | chr11 | 117362920 | ||||||
chr11:117363122
|
A | G | 1 | a0001c0002t0002g0164 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.688-307A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 7/32 | chr11 | 117363122 | ||||||
chr11:117363347
|
C | T | 2 | a0002c0001t0003g0178a0002c0001t0003g0179 | 2 | NA18967.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.688-82C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 7/32 | chr11 | 117363347 | ||||||
chr11:117363646
|
G | T | 2 | a0003c0003t0002g0128a0003c0003t0004g0127 | 2 | NA18960.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.765+140G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117363646 | ||||||
chr11:117363668
|
A | G | 1 | a0001c0002t0001g0071 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.765+162A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117363668 | ||||||
chr11:117363759
|
C | CT | 88 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0042others(85): Show | 90 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.765+281dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117363759 | |||||
chr11:117363759
|
C | CTT | 13 | a0001c0002t0001g0041a0002c0001t0003g0179a0002c0001t0003g0211others(10): Show | 13 | HG02559.hp1 HG02572.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.765+280_765+281dup others(2): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117363759 | |||||
chr11:117363759
|
C | CTTT | 42 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0074others(39): Show | 44 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.765+279_765+281dup others(3): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117363759 | |||||
chr11:117363759
|
C | CTTTT | 9 | a0003c0003t0004g0052a0003c0003t0004g0108a0003c0003t0004g0131others(6): Show | 9 | HG00741.hp1 HG01358.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.765+278_765+281dup others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117363759 | |||||
chr11:117363759
|
C | CTTTTT | 7 | a0003c0003t0004g0034a0003c0003t0004g0035a0003c0003t0004g0136others(4): Show | 7 | HG00408.hp1 HG03453.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.765+277_765+281dup others(5): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117363759 | |||||
chr11:117363759
|
CT | C | 14 | a0001c0002t0001g0253a0001c0002t0002g0340a0001c0005t0005g0329others(11): Show | 14 | HG00323.hp1 HG01167.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.765+281delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117363759 | |||||
chr11:117363759
|
CTTTTTTT | C | 12 | a0002c0001t0003g0002a0002c0001t0003g0092a0002c0001t0003g0185others(9): Show | 15 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.765+275_765+281del others(7): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117363759 | |||||
chr11:117363759
|
CTTTTTTT others(5): Show |
C | 5 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.765+270_765+281del others(12): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117363759 | |||||
chr11:117363962
|
C | A | 9 | a0006c0007t0006g0029a0006c0007t0006g0030a0006c0007t0006g0265others(6): Show | 9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.765+456C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117363962 | ||||||
chr11:117364276
|
G | A | 1 | a0002c0001t0003g0190 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.765+770G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117364276 | ||||||
chr11:117364565
|
CT | C | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.765+1075delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117364565 | |||||
chr11:117364649
|
G | A | 9 | a0006c0007t0006g0029a0006c0007t0006g0030a0006c0007t0006g0265others(6): Show | 9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.765+1143G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117364649 | ||||||
chr11:117364652
|
G | A | 67 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(64): Show | 72 | HG00639.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.765+1146G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117364652 | ||||||
chr11:117364696
|
C | T | 81 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.765+1190C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117364696 | ||||||
chr11:117364744
|
T | A | 1 | a0021c0033t0001g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.765+1238T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117364744 | ||||||
chr11:117364893
|
C | T | 1 | a0002c0001t0001g0063 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.765+1387C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117364893 | ||||||
chr11:117364931
|
C | T | 80 | a0001c0002t0001g0326a0001c0002t0002g0001a0001c0002t0002g0008others(77): Show | 88 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.765+1425C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117364931 | ||||||
chr11:117365031
|
G | A | 7 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(4): Show | 7 | HG02145.hp1 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.765+1525G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365031 | ||||||
chr11:117365038
|
G | A | 1 | a0004c0004t0001g0300 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.765+1532G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365038 | ||||||
chr11:117365151
|
G | T | 1 | a0001c0005t0005g0331 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.765+1645G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365151 | ||||||
chr11:117365344
|
C | T | 66 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(63): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.765+1838C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365344 | ||||||
chr11:117365444
|
T | A | 1 | a0004c0004t0001g0332 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.765+1938T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365444 | ||||||
chr11:117365496
|
G | A | 2 | a0002c0001t0003g0134a0002c0001t0003g0135 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.765+1990G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365496 | ||||||
chr11:117365522
|
A | G | 4 | a0001c0005t0005g0329a0001c0005t0005g0331a0001c0005t0025g0078others(1): Show | 4 | HG01123.hp1 HG01346.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.765+2016A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365522 | ||||||
chr11:117365567
|
A | ATTTC | 62 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(59): Show | 64 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.765+2081_765+2084d others(6): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117365567 | |||||
chr11:117365603
|
G | T | 66 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(63): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.765+2097G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365603 | ||||||
chr11:117365715
|
G | A | 1 | a0002c0001t0003g0260 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.765+2209G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365715 | ||||||
chr11:117365799
|
C | T | 4 | a0003c0003t0004g0137a0003c0003t0004g0138a0003c0003t0004g0139others(1): Show | 4 | HG00408.hp1 NA19002.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.765+2293C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365799 | ||||||
chr11:117365831
|
C | T | 3 | a0011c0014t0013g0183a0011c0014t0013g0254a0026c0035t0013g0046 | 3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.765+2325C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365831 | ||||||
chr11:117365883
|
A | C | 3 | a0008c0011t0012g0080a0008c0011t0012g0081a0025c0029t0012g0079 | 3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.765+2377A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365883 | ||||||
chr11:117366200
|
G | T | 1 | a0002c0001t0001g0014 | 2 | NA18966.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.765+2694G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366200 | ||||||
chr11:117366470
|
G | A | 4 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(1): Show | 4 | HG01884.hp1 HG02683.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.765+2964G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366470 | ||||||
chr11:117366491
|
C | G | 35 | a0004c0004t0001g0015a0004c0004t0001g0016a0004c0004t0001g0027others(32): Show | 36 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.765+2985C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366491 | ||||||
chr11:117366501
|
C | T | 1 | a0008c0011t0012g0081 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.765+2995C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366501 | ||||||
chr11:117366548
|
C | A | 1 | a0001c0013t0005g0279 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.765+3042C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366548 | ||||||
chr11:117366587
|
G | A | 1 | a0001c0002t0001g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.765+3081G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366587 | ||||||
chr11:117366620
|
G | A | 9 | a0006c0007t0006g0029a0006c0007t0006g0030a0006c0007t0006g0265others(6): Show | 9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.765+3114G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366620 | ||||||
chr11:117366639
|
G | C | 3 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0026 | 3 | HG01884.hp1 HG02683.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.765+3133G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366639 | ||||||
chr11:117366771
|
A | G | 82 | a0001c0002t0004g0069a0003c0003t0002g0128a0003c0003t0004g0006others(79): Show | 84 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.765+3265A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366771 | ||||||
chr11:117366905
|
A | G | 2 | a0003c0003t0004g0120a0003c0003t0004g0229 | 2 | HG01978.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.765+3399A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366905 | ||||||
chr11:117367111
|
G | A | 1 | a0002c0001t0024g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.765+3605G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117367111 | ||||||
chr11:117367226
|
C | T | 1 | a0001c0002t0002g0347 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.765+3720C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117367226 | ||||||
chr11:117367395
|
G | A | 3 | a0011c0014t0013g0183a0011c0014t0013g0254a0026c0035t0013g0046 | 3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.766-3685G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117367395 | ||||||
chr11:117367762
|
G | A | 79 | a0001c0002t0001g0326a0001c0002t0002g0001a0001c0002t0002g0008others(76): Show | 87 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.766-3318G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117367762 | ||||||
chr11:117367775
|
C | T | 85 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0004g0069others(82): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.766-3305C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117367775 | ||||||
chr11:117367810
|
A | T | 5 | a0001c0002t0001g0050a0001c0002t0001g0252a0001c0002t0001g0253others(2): Show | 5 | HG01069.hp2 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3270A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117367810 | ||||||
chr11:117368281
|
T | C | 1 | a0004c0009t0008g0023 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.766-2799T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117368281 | ||||||
chr11:117368457
|
A | C | 88 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0004g0069others(85): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.766-2623A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117368457 | ||||||
chr11:117368474
|
G | T | 85 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0004g0069others(82): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.766-2606G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117368474 | ||||||
chr11:117368557
|
C | T | 6 | a0001c0002t0002g0237a0005c0006t0007g0048a0005c0006t0007g0049others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.766-2523C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117368557 | ||||||
chr11:117368618
|
C | T | 11 | a0002c0001t0003g0002a0002c0001t0003g0185a0002c0001t0003g0186others(8): Show | 14 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.766-2462C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117368618 | ||||||
chr11:117368640
|
C | T | 1 | a0002c0001t0003g0096 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.766-2440C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117368640 | ||||||
chr11:117369046
|
A | G | 1 | a0009c0020t0014g0327 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.766-2034A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117369046 | ||||||
chr11:117369047
|
T | C | 2 | a0001c0002t0002g0019a0001c0002t0002g0353 | 3 | NA18944.hp1 NA19007.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.766-2033T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117369047 | ||||||
chr11:117369068
|
C | T | 1 | a0004c0004t0001g0295 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.766-2012C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117369068 | ||||||
chr11:117369286
|
C | T | 5 | a0001c0002t0001g0050a0001c0002t0001g0252a0001c0002t0001g0253others(2): Show | 5 | HG01069.hp2 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-1794C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117369286 | ||||||
chr11:117369354
|
A | G | 1 | a0004c0004t0001g0285 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.766-1726A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117369354 | ||||||
chr11:117369498
|
G | T | 5 | a0001c0002t0001g0050a0001c0002t0001g0252a0001c0002t0001g0253others(2): Show | 5 | HG01069.hp2 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-1582G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117369498 | ||||||
chr11:117369641
|
G | A | 85 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0004g0069others(82): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.766-1439G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117369641 | ||||||
chr11:117370132
|
C | T | 1 | a0001c0002t0002g0314 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.766-948C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370132 | ||||||
chr11:117370134
|
T | C | 1 | a0013c0018t0014g0269 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.766-946T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370134 | ||||||
chr11:117370331
|
A | G | 1 | a0003c0003t0004g0106 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.766-749A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370331 | ||||||
chr11:117370437
|
A | G | 1 | a0001c0002t0001g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.766-643A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370437 | ||||||
chr11:117370499
|
C | T | 5 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.766-581C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370499 | ||||||
chr11:117370598
|
G | A | 1 | a0002c0001t0001g0282 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.766-482G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370598 | ||||||
chr11:117370681
|
C | T | 1 | a0002c0001t0003g0198 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.766-399C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370681 | ||||||
chr11:117370682
|
G | A | 1 | a0002c0001t0003g0011 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.766-398G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370682 | ||||||
chr11:117370713
|
C | T | 42 | a0001c0002t0001g0070a0001c0002t0001g0071a0002c0001t0001g0053others(39): Show | 43 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.766-367C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370713 | ||||||
chr11:117370939
|
G | A | 1 | a0005c0006t0007g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.766-141G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370939 | ||||||
chr11:117371012
|
T | C | 2 | a0004c0004t0001g0027a0004c0004t0001g0312 | 2 | NA18968.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.766-68T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117371012 | ||||||
chr11:117371044
|
T | A | 194 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0003g0177others(191): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.766-36T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117371044 | ||||||
chr11:117371763
|
C | T | 1 | a0001c0005t0005g0032 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1152+297C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117371763 | ||||||
chr11:117371795
|
C | CT | 236 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(233): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1152+344dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr11 | 117371795 | |||||
chr11:117371795
|
C | CTT | 9 | a0002c0001t0001g0054a0002c0001t0003g0179a0003c0003t0004g0034others(6): Show | 9 | HG00738.hp1 HG01358.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1152+343_1152+344d others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr11 | 117371795 | |||||
chr11:117372050
|
A | T | 1 | a0003c0003t0005g0118 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1152+584A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117372050 | ||||||
chr11:117372108
|
A | AT | 57 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(54): Show | 58 | HG00639.hp2 HG00738.hp1 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.1152+659dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr11 | 117372108 | |||||
chr11:117372108
|
A | ATT | 79 | a0002c0001t0001g0072a0002c0001t0001g0090a0003c0003t0002g0128others(76): Show | 81 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1152+658_1152+659d others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr11 | 117372108 | |||||
chr11:117372108
|
A | ATTT | 101 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0002g0044others(98): Show | 112 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1152+657_1152+659d others(5): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr11 | 117372108 | |||||
chr11:117372299
|
C | T | 1 | a0002c0001t0003g0264 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1152+833C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117372299 | ||||||
chr11:117372373
|
A | C | 1 | a0003c0003t0004g0074 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1152+907A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117372373 | ||||||
chr11:117372423
|
C | CT | 14 | a0004c0004t0001g0287a0004c0004t0001g0288a0004c0004t0001g0289others(11): Show | 14 | HG00639.hp2 HG01099.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1152+968dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr11 | 117372423 | |||||
chr11:117372480
|
C | T | 1 | a0001c0002t0022g0343 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1152+1014C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117372480 | ||||||
chr11:117372501
|
C | T | 11 | a0002c0001t0003g0002a0002c0001t0003g0185a0002c0001t0003g0186others(8): Show | 14 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.1152+1035C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117372501 | ||||||
chr11:117373013
|
T | C | 3 | a0002c0001t0003g0205a0002c0001t0003g0206a0002c0001t0003g0208 | 3 | NA18946.hp2 NA19078.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1153-738T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373013 | ||||||
chr11:117373037
|
A | G | 4 | a0001c0005t0005g0329a0001c0005t0005g0331a0001c0005t0025g0078others(1): Show | 4 | HG01123.hp1 HG01346.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153-714A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373037 | ||||||
chr11:117373107
|
G | A | 3 | a0001c0002t0002g0320a0002c0001t0003g0134a0002c0001t0003g0135 | 3 | HG02809.hp1 HG03516.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1153-644G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373107 | ||||||
chr11:117373323
|
C | T | 9 | a0006c0007t0006g0029a0006c0007t0006g0030a0006c0007t0006g0265others(6): Show | 9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.1153-428C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373323 | ||||||
chr11:117373363
|
GA | G | 9 | a0001c0002t0001g0326a0001c0002t0002g0170a0001c0002t0002g0320others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1153-375delA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr11 | 117373363 | |||||
chr11:117373456
|
C | A | 2 | a0002c0001t0003g0187a0002c0001t0003g0188 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1153-295C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373456 | ||||||
chr11:117373539
|
C | A | 10 | a0002c0001t0001g0004a0002c0001t0001g0053a0002c0001t0001g0054others(7): Show | 11 | HG00099.hp1 HG00741.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1153-212C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373539 | ||||||
chr11:117373575
|
C | T | 4 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(1): Show | 4 | HG01884.hp1 HG02683.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153-176C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373575 | ||||||
chr11:117373577
|
T | C | 5 | a0001c0002t0001g0326a0001c0002t0002g0170a0001c0002t0002g0320others(2): Show | 5 | NA18941.hp2 NA18970.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153-174T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373577 | ||||||
chr11:117373609
|
C | T | 1 | a0002c0001t0001g0091 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1153-142C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373609 | ||||||
chr11:117373663
|
C | T | 1 | a0005c0006t0007g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1153-88C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373663 | ||||||
chr11:117373890
|
A | T | 4 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(1): Show | 4 | HG01884.hp1 HG02683.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+59A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117373890 | ||||||
chr11:117373931
|
G | A | 2 | a0003c0003t0004g0120a0003c0003t0004g0229 | 2 | HG01978.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1233+100G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117373931 | ||||||
chr11:117374299
|
G | A | 1 | a0009c0021t0019g0082 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1233+468G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117374299 | ||||||
chr11:117374417
|
C | T | 126 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(123): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1233+586C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117374417 | ||||||
chr11:117374575
|
G | A | 1 | a0008c0011t0007g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1233+744G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117374575 | ||||||
chr11:117374780
|
G | A | 1 | a0009c0020t0014g0327 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1234-928G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117374780 | ||||||
chr11:117375008
|
C | T | 1 | a0001c0002t0002g0018 | 2 | HG01346.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1234-700C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117375008 | ||||||
chr11:117375102
|
G | C | 1 | a0019c0025t0001g0303 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1234-606G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117375102 | ||||||
chr11:117375272
|
C | T | 38 | a0001c0002t0001g0037a0001c0002t0002g0001a0001c0002t0002g0008others(35): Show | 42 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.1234-436C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117375272 | ||||||
chr11:117375326
|
G | A | 1 | a0001c0002t0002g0321 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1234-382G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117375326 | ||||||
chr11:117375349
|
G | A | 2 | a0002c0001t0003g0134a0002c0001t0003g0135 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1234-359G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117375349 | ||||||
chr11:117375434
|
T | C | 155 | a0001c0002t0003g0177a0001c0002t0004g0069a0002c0001t0003g0002others(152): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.1234-274T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117375434 | ||||||
chr11:117375687
|
T | G | 3 | a0005c0006t0008g0045a0009c0020t0014g0327a0013c0018t0014g0269 | 3 | HG02559.hp1 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1234-21T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117375687 | ||||||
chr11:117375850
|
G | A | 2 | a0001c0002t0001g0070a0001c0002t0001g0071 | 2 | HG01123.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1317+59G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117375850 | ||||||
chr11:117376160
|
T | C | 37 | a0002c0001t0001g0004a0002c0001t0001g0013a0002c0001t0001g0014others(34): Show | 43 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1317+369T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117376160 | ||||||
chr11:117376199
|
C | G | 1 | a0005c0006t0007g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1317+408C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117376199 | ||||||
chr11:117376246
|
T | A | 1 | a0020c0028t0004g0155 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1317+455T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117376246 | ||||||
chr11:117376248
|
GTCCTGGA others(17): Show |
G | 1 | a0004c0004t0001g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1317+462_1317+485d others(26): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr11 | 117376248 | |||||
chr11:117376312
|
C | T | 1 | a0002c0001t0003g0221 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1317+521C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117376312 | ||||||
chr11:117376510
|
A | G | 2 | a0003c0003t0005g0309a0003c0003t0005g0328 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1317+719A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117376510 | ||||||
chr11:117376595
|
CCAGCCTT others(29): Show |
C | 7 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(4): Show | 7 | HG02145.hp1 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1317+844_1317+879d others(38): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr11 | 117376595 | |||||
chr11:117376829
|
G | A | 3 | a0008c0011t0012g0080a0008c0011t0012g0081a0025c0029t0012g0079 | 3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1317+1038G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117376829 | ||||||
chr11:117376885
|
A | G | 1 | a0006c0007t0006g0029 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1317+1094A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117376885 | ||||||
chr11:117377048
|
G | A | 1 | a0004c0004t0001g0310 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1317+1257G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377048 | ||||||
chr11:117377048
|
G | C | 1 | a0008c0011t0007g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1317+1257G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377048 | ||||||
chr11:117377187
|
C | CCA | 239 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(236): Show | 252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.1317+1397_1317+139 others(6): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr11 | 117377187 | |||||
chr11:117377418
|
T | C | 2 | a0003c0003t0005g0007a0003c0022t0005g0227 | 3 | HG01261.hp2 HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1317+1627T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377418 | ||||||
chr11:117377509
|
G | C | 1 | a0002c0001t0003g0096 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1317+1718G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377509 | ||||||
chr11:117377517
|
G | A | 6 | a0001c0002t0002g0036a0001c0002t0002g0340a0001c0002t0002g0341others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1317+1726G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377517 | ||||||
chr11:117377552
|
G | A | 63 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(60): Show | 65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.1317+1761G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377552 | ||||||
chr11:117377626
|
G | A | 4 | a0001c0002t0002g0001a0001c0002t0002g0144a0001c0002t0002g0175others(1): Show | 7 | HG00544.hp2 HG02083.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1317+1835G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377626 | ||||||
chr11:117377635
|
A | G | 4 | a0001c0002t0002g0017a0001c0002t0002g0350a0001c0002t0002g0352others(1): Show | 5 | HG01952.hp1 HG01975.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1317+1844A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377635 | ||||||
chr11:117377698
|
C | A | 3 | a0011c0014t0013g0183a0011c0014t0013g0254a0026c0035t0013g0046 | 3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1317+1907C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377698 | ||||||
chr11:117377942
|
C | T | 6 | a0006c0007t0006g0265a0006c0007t0006g0267a0006c0007t0006g0270others(3): Show | 6 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.1317+2151C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377942 | ||||||
chr11:117377969
|
C | T | 1 | a0001c0002t0002g0346 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1317+2178C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377969 | ||||||
chr11:117378021
|
C | T | 1 | a0002c0001t0001g0014 | 2 | NA18966.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1317+2230C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117378021 | ||||||
chr11:117378115
|
C | T | 1 | a0001c0002t0002g0245 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1317+2324C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117378115 | ||||||
chr11:117378116
|
G | A | 17 | a0002c0001t0001g0004a0002c0001t0001g0053a0002c0001t0001g0054others(14): Show | 19 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1317+2325G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117378116 | ||||||
chr11:117378171
|
C | G | 1 | a0002c0001t0003g0255 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1317+2380C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117378171 | ||||||
chr11:117378268
|
C | T | 3 | a0004c0034t0007g0039a0008c0011t0007g0028a0024c0030t0021g0038 | 3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1318-2346C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117378268 | ||||||
chr11:117378360
|
C | CT | 5 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1318-2248dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr11 | 117378360 | |||||
chr11:117378402
|
G | T | 1 | a0001c0005t0005g0159 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1318-2212G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117378402 | ||||||
chr11:117378857
|
C | G | 1 | a0002c0001t0001g0054 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1318-1757C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117378857 | ||||||
chr11:117379170
|
G | A | 1 | a0004c0004t0001g0300 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1318-1444G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117379170 | ||||||
chr11:117379411
|
C | T | 1 | a0001c0005t0005g0250 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1318-1203C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117379411 | ||||||
chr11:117379703
|
T | G | 1 | a0002c0001t0001g0063 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1318-911T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117379703 | ||||||
chr11:117379709
|
G | T | 1 | a0003c0003t0004g0052 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1318-905G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117379709 | ||||||
chr11:117379814
|
G | A | 2 | a0003c0003t0004g0126a0003c0003t0004g0130 | 2 | HG00099.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.1318-800G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117379814 | ||||||
chr11:117379852
|
C | CT | 143 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(140): Show | 156 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.1318-739dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr11 | 117379852 | |||||
chr11:117379852
|
C | CTT | 9 | a0001c0002t0002g0017a0001c0002t0002g0350a0001c0002t0002g0352others(6): Show | 10 | HG01361.hp2 HG01433.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.1318-740_1318-739d others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr11 | 117379852 | |||||
chr11:117379852
|
CT | C | 30 | a0001c0005t0005g0085a0001c0005t0005g0086a0001c0005t0005g0159others(27): Show | 31 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(28): Show |
intron_variant | MODIFIER | c.1318-739delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr11 | 117379852 | |||||
chr11:117380033
|
C | T | 10 | a0004c0004t0001g0015a0004c0004t0001g0016a0004c0004t0001g0285others(7): Show | 11 | HG01081.hp2 HG01884.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1318-581C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117380033 | ||||||
chr11:117380170
|
G | A | 1 | a0002c0001t0003g0096 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1318-444G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117380170 | ||||||
chr11:117380221
|
C | T | 2 | a0003c0003t0005g0309a0003c0003t0005g0328 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1318-393C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117380221 | ||||||
chr11:117380427
|
A | G | 168 | a0001c0002t0003g0177a0002c0001t0001g0004a0002c0001t0001g0053others(165): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1318-187A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117380427 | ||||||
chr11:117380503
|
C | A | 13 | a0004c0004t0001g0015a0004c0004t0001g0016a0004c0004t0001g0285others(10): Show | 14 | HG01081.hp2 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1318-111C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117380503 | ||||||
chr11:117380786
|
C | T | 1 | a0003c0003t0004g0109 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1409+81C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117380786 | ||||||
chr11:117380805
|
G | C | 326 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(323): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1409+100G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117380805 | ||||||
chr11:117380851
|
C | T | 1 | a0001c0002t0002g0352 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1409+146C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117380851 | ||||||
chr11:117380867
|
G | A | 1 | a0014c0019t0004g0051 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1409+162G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117380867 | ||||||
chr11:117380897
|
T | G | 1 | a0002c0001t0003g0209 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1409+192T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117380897 | ||||||
chr11:117381105
|
T | G | 1 | a0001c0002t0005g0241 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1409+400T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117381105 | ||||||
chr11:117381324
|
C | T | 2 | a0009c0021t0019g0082a0023c0032t0020g0193 | 2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1410-377C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117381324 | ||||||
chr11:117381371
|
C | T | 3 | a0002c0001t0003g0213a0002c0001t0003g0214a0002c0001t0003g0218 | 3 | HG01069.hp1 HG01071.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1410-330C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117381371 | ||||||
chr11:117381419
|
G | A | 1 | a0001c0002t0002g0142 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1410-282G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117381419 | ||||||
chr11:117381519
|
A | C | 2 | a0003c0003t0005g0309a0003c0003t0005g0328 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1410-182A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117381519 | ||||||
chr11:117381609
|
A | G | 1 | a0020c0028t0004g0155 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1410-92A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117381609 | ||||||
chr11:117382245
|
T | G | 1 | a0003c0003t0004g0112 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1577+377T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 13/32 | chr11 | 117382245 | ||||||
chr11:117382514
|
C | T | 4 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(1): Show | 4 | HG01884.hp1 HG02683.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1578-282C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 13/32 | chr11 | 117382514 | ||||||
chr11:117382556
|
G | A | 3 | a0004c0034t0007g0039a0008c0011t0007g0028a0024c0030t0021g0038 | 3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1578-240G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 13/32 | chr11 | 117382556 | ||||||
chr11:117382764
|
T | C | 1 | a0002c0001t0003g0204 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1578-32T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 13/32 | chr11 | 117382764 | ||||||
chr11:117383013
|
T | C | 3 | a0008c0011t0012g0080a0008c0011t0012g0081a0025c0029t0012g0079 | 3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1724+71T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117383013 | ||||||
chr11:117383352
|
T | C | 1 | a0001c0036t0005g0161 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1724+410T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117383352 | ||||||
chr11:117383406
|
G | A | 13 | a0002c0001t0001g0004a0002c0001t0001g0053a0002c0001t0001g0054others(10): Show | 14 | HG00099.hp1 HG00741.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1724+464G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117383406 | ||||||
chr11:117383896
|
C | T | 1 | a0002c0001t0001g0014 | 2 | NA18966.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1724+954C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117383896 | ||||||
chr11:117383973
|
T | G | 1 | a0004c0004t0001g0065 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1724+1031T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117383973 | ||||||
chr11:117384483
|
T | C | 1 | a0003c0022t0005g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1724+1541T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117384483 | ||||||
chr11:117384567
|
C | T | 17 | a0001c0002t0001g0050a0001c0002t0001g0070a0001c0002t0001g0071others(14): Show | 19 | HG01069.hp2 HG01123.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1724+1625C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117384567 | ||||||
chr11:117384607
|
C | A | 3 | a0002c0001t0003g0220a0002c0001t0003g0221a0002c0001t0003g0222 | 3 | HG00438.hp1 HG00558.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.1724+1665C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117384607 | ||||||
chr11:117384670
|
C | T | 2 | a0004c0015t0003g0024a0004c0015t0003g0025 | 2 | HG00323.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1724+1728C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117384670 | ||||||
chr11:117384921
|
C | T | 1 | a0002c0001t0003g0204 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1724+1979C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117384921 | ||||||
chr11:117384966
|
T | C | 1 | a0001c0002t0001g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1724+2024T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117384966 | ||||||
chr11:117384971
|
G | A | 2 | a0002c0001t0003g0214a0002c0001t0003g0218 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1724+2029G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117384971 | ||||||
chr11:117385121
|
G | A | 1 | a0001c0002t0002g0142 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1725-2082G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385121 | ||||||
chr11:117385134
|
C | T | 2 | a0007c0010t0002g0168a0007c0010t0002g0174 | 2 | HG01074.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1725-2069C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385134 | ||||||
chr11:117385171
|
C | T | 2 | a0002c0001t0003g0134a0002c0001t0003g0135 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1725-2032C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385171 | ||||||
chr11:117385283
|
T | C | 1 | a0001c0005t0005g0272 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1725-1920T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385283 | ||||||
chr11:117385412
|
G | A | 1 | a0001c0005t0005g0355 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1725-1791G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385412 | ||||||
chr11:117385414
|
G | A | 1 | a0001c0002t0002g0238 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1725-1789G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385414 | ||||||
chr11:117385509
|
T | C | 5 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1725-1694T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385509 | ||||||
chr11:117385650
|
G | A | 1 | a0002c0001t0001g0282 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1725-1553G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385650 | ||||||
chr11:117385668
|
C | G | 188 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(185): Show | 200 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.1725-1535C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385668 | ||||||
chr11:117385720
|
T | C | 144 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0044others(141): Show | 157 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1725-1483T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385720 | ||||||
chr11:117385763
|
G | C | 1 | a0003c0003t0004g0125 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1725-1440G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385763 | ||||||
chr11:117385864
|
A | G | 5 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1725-1339A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385864 | ||||||
chr11:117385973
|
T | G | 3 | a0008c0011t0012g0080a0008c0011t0012g0081a0025c0029t0012g0079 | 3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1725-1230T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385973 | ||||||
chr11:117386367
|
G | A | 3 | a0005c0006t0008g0045a0009c0020t0014g0327a0013c0018t0014g0269 | 3 | HG02559.hp1 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1725-836G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117386367 | ||||||
chr11:117386462
|
A | G | 9 | a0006c0007t0006g0029a0006c0007t0006g0030a0006c0007t0006g0265others(6): Show | 9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.1725-741A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117386462 | ||||||
chr11:117386705
|
T | G | 3 | a0008c0011t0012g0080a0008c0011t0012g0081a0025c0029t0012g0079 | 3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1725-498T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117386705 | ||||||
chr11:117386860
|
A | G | 3 | a0011c0014t0013g0183a0011c0014t0013g0254a0026c0035t0013g0046 | 3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1725-343A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117386860 | ||||||
chr11:117387015
|
A | G | 1 | a0006c0007t0006g0029 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1725-188A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117387015 | ||||||
chr11:117387117
|
G | A | 1 | a0001c0002t0001g0326 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1725-86G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117387117 | ||||||
chr11:117387160
|
G | T | 76 | a0001c0002t0001g0326a0001c0002t0002g0001a0001c0002t0002g0008others(73): Show | 84 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1725-43G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117387160 | ||||||
chr11:117387482
|
T | C | 122 | a0001c0002t0003g0177a0002c0001t0001g0004a0002c0001t0001g0013others(119): Show | 133 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1934+70T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117387482 | ||||||
chr11:117387929
|
A | C | 5 | a0001c0002t0001g0326a0001c0002t0002g0170a0001c0002t0002g0320others(2): Show | 5 | NA18941.hp2 NA18970.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.1934+517A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117387929 | ||||||
chr11:117387946
|
C | G | 6 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(3): Show | 6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1934+534C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117387946 | ||||||
chr11:117387971
|
G | T | 6 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(3): Show | 6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1934+559G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117387971 | ||||||
chr11:117388218
|
G | C | 3 | a0008c0011t0012g0080a0008c0011t0012g0081a0025c0029t0012g0079 | 3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1934+806G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117388218 | ||||||
chr11:117388471
|
T | G | 1 | a0001c0005t0005g0163 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1934+1059T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117388471 | ||||||
chr11:117388479
|
C | T | 1 | a0001c0005t0005g0032 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1934+1067C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117388479 | ||||||
chr11:117388771
|
CT | C | 203 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(200): Show | 218 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.1934+1373delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr11 | 117388771 | |||||
chr11:117388834
|
C | T | 1 | a0004c0004t0001g0300 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1934+1422C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117388834 | ||||||
chr11:117388910
|
C | T | 2 | a0004c0004t0001g0315a0004c0004t0001g0316 | 2 | HG02155.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1934+1498C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117388910 | ||||||
chr11:117388939
|
T | A | 1 | a0003c0003t0005g0328 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1934+1527T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117388939 | ||||||
chr11:117388940
|
T | TA | 3 | a0004c0034t0007g0039a0008c0011t0007g0028a0024c0030t0021g0038 | 3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1934+1528_1934+152 others(5): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117388940 | ||||||
chr11:117389022
|
G | C | 4 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(1): Show | 4 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1934+1610G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117389022 | ||||||
chr11:117389066
|
G | A | 29 | a0002c0001t0003g0066a0002c0001t0003g0092a0002c0001t0003g0096others(26): Show | 29 | HG00408.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1934+1654G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117389066 | ||||||
chr11:117389188
|
C | T | 2 | a0004c0004t0001g0287a0004c0004t0001g0288 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1935-1589C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117389188 | ||||||
chr11:117389223
|
C | T | 3 | a0004c0034t0007g0039a0008c0011t0007g0028a0024c0030t0021g0038 | 3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1935-1554C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117389223 | ||||||
chr11:117389359
|
A | G | 120 | a0002c0001t0001g0004a0002c0001t0001g0013a0002c0001t0001g0014others(117): Show | 131 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1935-1418A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117389359 | ||||||
chr11:117389464
|
G | T | 9 | a0006c0007t0006g0029a0006c0007t0006g0030a0006c0007t0006g0265others(6): Show | 9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.1935-1313G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117389464 | ||||||
chr11:117389553
|
C | T | 1 | a0001c0005t0005g0033 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1935-1224C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117389553 | ||||||
chr11:117389788
|
G | A | 76 | a0002c0001t0003g0002a0002c0001t0003g0010a0002c0001t0003g0012others(73): Show | 81 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.1935-989G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117389788 | ||||||
chr11:117389926
|
G | A | 2 | a0001c0002t0002g0152a0002c0001t0001g0063 | 2 | HG02040.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1935-851G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117389926 | ||||||
chr11:117389938
|
C | CT | 19 | a0001c0002t0002g0145a0001c0002t0002g0235a0001c0002t0002g0238others(16): Show | 20 | HG00423.hp2 HG01106.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.1935-818dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr11 | 117389938 | |||||
chr11:117389938
|
CT | C | 167 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0042others(164): Show | 179 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.1935-818delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr11 | 117389938 | |||||
chr11:117389938
|
CTT | C | 10 | a0001c0002t0001g0050a0001c0002t0001g0070a0001c0002t0001g0071others(7): Show | 10 | HG01069.hp2 HG01123.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1935-819_1935-818d others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr11 | 117389938 | |||||
chr11:117390001
|
G | A | 1 | a0010c0012t0006g0266 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1935-776G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390001 | ||||||
chr11:117390034
|
C | T | 1 | a0001c0002t0005g0241 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1935-743C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390034 | ||||||
chr11:117390085
|
G | A | 1 | a0003c0003t0004g0101 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1935-692G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390085 | ||||||
chr11:117390235
|
G | C | 3 | a0011c0014t0013g0183a0011c0014t0013g0254a0026c0035t0013g0046 | 3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1935-542G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390235 | ||||||
chr11:117390285
|
C | T | 1 | a0001c0005t0005g0055 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1935-492C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390285 | ||||||
chr11:117390299
|
G | T | 1 | a0002c0001t0003g0185 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1935-478G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390299 | ||||||
chr11:117390310
|
G | A | 1 | a0002c0001t0001g0056 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1935-467G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390310 | ||||||
chr11:117390558
|
C | A | 1 | a0002c0001t0003g0185 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1935-219C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390558 | ||||||
chr11:117390642
|
GA | G | 77 | a0002c0001t0003g0002a0002c0001t0003g0010a0002c0001t0003g0012others(74): Show | 82 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1935-120delA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr11 | 117390642 | |||||
chr11:117390643
|
A | G | 1 | a0002c0001t0003g0185 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1935-134A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390643 | ||||||
chr11:117390772
|
C | G | 39 | a0003c0003t0002g0128a0003c0003t0004g0006a0003c0003t0004g0034others(36): Show | 40 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(37): Show |
splice_region_variant&intron_variant | LOW | c.1935-5C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390772 | ||||||
chr11:117390970
|
C | T | 1 | a0001c0002t0002g0171 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2067-29C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 16/32 | chr11 | 117390970 | ||||||
chr11:117391238
|
T | A | 1 | a0008c0011t0007g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2283+23T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 17/32 | chr11 | 117391238 | ||||||
chr11:117391436
|
A | C | 1 | a0002c0001t0001g0053 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2283+221A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 17/32 | chr11 | 117391436 | ||||||
chr11:117391668
|
C | G | 1 | a0001c0002t0002g0321 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2283+453C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 17/32 | chr11 | 117391668 | ||||||
chr11:117391742
|
G | A | 3 | a0011c0014t0013g0183a0011c0014t0013g0254a0026c0035t0013g0046 | 3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2284-484G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 17/32 | chr11 | 117391742 | ||||||
chr11:117391882
|
C | T | 96 | a0002c0001t0003g0002a0002c0001t0003g0010a0002c0001t0003g0011others(93): Show | 102 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.2284-344C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 17/32 | chr11 | 117391882 | ||||||
chr11:117391981
|
G | A | 1 | a0002c0001t0003g0202 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2284-245G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 17/32 | chr11 | 117391981 | ||||||
chr11:117392068
|
G | T | 1 | a0002c0001t0003g0204 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2284-158G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 17/32 | chr11 | 117392068 | ||||||
chr11:117392151
|
A | G | 2 | a0003c0003t0011g0119a0003c0003t0011g0123 | 2 | HG00140.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2284-75A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 17/32 | chr11 | 117392151 | ||||||
chr11:117392387
|
T | C | 88 | a0002c0001t0003g0002a0002c0001t0003g0010a0002c0001t0003g0011others(85): Show | 94 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.2361+84T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 18/32 | chr11 | 117392387 | ||||||
chr11:117392655
|
G | C | 1 | a0002c0001t0024g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2493+28G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 19/32 | chr11 | 117392655 | ||||||
chr11:117392833
|
G | A | 1 | a0019c0025t0001g0303 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2494-171G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 19/32 | chr11 | 117392833 | ||||||
chr11:117392900
|
T | G | 88 | a0002c0001t0003g0002a0002c0001t0003g0010a0002c0001t0003g0011others(85): Show | 94 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.2494-104T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 19/32 | chr11 | 117392900 | ||||||
chr11:117393155
|
G | GCACACAC others(5): Show |
2 | a0002c0001t0003g0214a0002c0001t0003g0218 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2616+43_2616+54dup others(12): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | INFO_REALIGN_3_PRIME | chr11 | 117393155 | |||||
chr11:117393158
|
C | T | 4 | a0007c0010t0002g0167a0007c0010t0002g0168a0007c0010t0002g0174others(1): Show | 4 | HG01074.hp2 HG01081.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.2616+32C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | chr11 | 117393158 | ||||||
chr11:117393204
|
C | T | 1 | a0005c0006t0007g0076 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2616+78C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | chr11 | 117393204 | ||||||
chr11:117393486
|
C | T | 5 | a0003c0003t0004g0104a0003c0003t0004g0105a0003c0003t0004g0106others(2): Show | 5 | HG02698.hp2 HG03239.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.2616+360C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | chr11 | 117393486 | ||||||
chr11:117393540
|
G | A | 6 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(3): Show | 6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2616+414G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | chr11 | 117393540 | ||||||
chr11:117393742
|
T | C | 4 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(1): Show | 4 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2617-608T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | chr11 | 117393742 | ||||||
chr11:117394258
|
C | T | 2 | a0003c0003t0004g0105a0003c0003t0004g0108 | 2 | HG03831.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2617-92C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | chr11 | 117394258 | ||||||
chr11:117394298
|
T | C | 1 | a0002c0001t0024g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2617-52T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | chr11 | 117394298 | ||||||
chr11:117394328
|
G | A | 1 | a0003c0003t0004g0112 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2617-22G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | chr11 | 117394328 | ||||||
chr11:117394332
|
G | A | 2 | a0007c0010t0002g0168a0007c0010t0002g0174 | 2 | HG01074.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2617-18G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | chr11 | 117394332 | ||||||
chr11:117395067
|
G | T | 1 | a0021c0033t0001g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2845-56G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 22/32 | chr11 | 117395067 | ||||||
chr11:117395350
|
C | T | 2 | a0008c0011t0012g0080a0008c0011t0012g0081 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2913+159C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 23/32 | chr11 | 117395350 | ||||||
chr11:117395378
|
G | A | 81 | a0002c0001t0001g0004a0002c0001t0001g0053a0002c0001t0001g0054others(78): Show | 88 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2914-169G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 23/32 | chr11 | 117395378 | ||||||
chr11:117395479
|
G | A | 1 | a0002c0001t0003g0097 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2914-68G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 23/32 | chr11 | 117395479 | ||||||
chr11:117395750
|
T | C | 14 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(11): Show | 14 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.3089+28T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 24/32 | chr11 | 117395750 | ||||||
chr11:117395932
|
G | C | 118 | a0001c0002t0003g0177a0002c0001t0001g0004a0002c0001t0001g0013others(115): Show | 127 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.3090-122G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 24/32 | chr11 | 117395932 | ||||||
chr11:117395938
|
T | C | 3 | a0004c0034t0007g0039a0008c0011t0007g0028a0024c0030t0021g0038 | 3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3090-116T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 24/32 | chr11 | 117395938 | ||||||
chr11:117396006
|
C | A | 1 | a0001c0002t0002g0337 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3090-48C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 24/32 | chr11 | 117396006 | ||||||
chr11:117396006
|
C | G | 6 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(3): Show | 6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.3090-48C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 24/32 | chr11 | 117396006 | ||||||
chr11:117396038
|
A | C | 189 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(186): Show | 201 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.3090-16A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 24/32 | chr11 | 117396038 | ||||||
chr11:117396185
|
GCTGGGGG others(7): Show |
G | 1 | a0001c0002t0023g0242 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3216+20_3216+33del others(14): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 25/32 | INFO_REALIGN_3_PRIME | chr11 | 117396185 | |||||
chr11:117396721
|
G | T | 2 | a0002c0001t0003g0134a0002c0001t0003g0135 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3278+110G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 26/32 | chr11 | 117396721 | ||||||
chr11:117396924
|
C | T | 1 | a0001c0005t0005g0173 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3279-167C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 26/32 | chr11 | 117396924 | ||||||
chr11:117397056
|
G | T | 1 | a0002c0001t0024g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3279-35G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 26/32 | chr11 | 117397056 | ||||||
chr11:117397358
|
C | G | 28 | a0002c0001t0003g0066a0002c0001t0003g0092a0002c0001t0003g0176others(25): Show | 28 | HG00408.hp2 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.3501+45C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117397358 | ||||||
chr11:117397540
|
G | T | 6 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(3): Show | 6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.3501+227G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117397540 | ||||||
chr11:117397740
|
C | T | 2 | a0011c0014t0013g0183a0011c0014t0013g0254 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3501+427C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117397740 | ||||||
chr11:117397820
|
G | A | 1 | a0001c0005t0005g0355 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3501+507G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117397820 | ||||||
chr11:117397826
|
C | T | 1 | a0001c0002t0002g0340 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3501+513C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117397826 | ||||||
chr11:117397880
|
C | G | 3 | a0002c0001t0003g0213a0002c0001t0003g0214a0002c0001t0003g0218 | 3 | HG01069.hp1 HG01071.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.3501+567C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117397880 | ||||||
chr11:117397923
|
C | T | 1 | a0004c0004t0001g0288 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3501+610C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117397923 | ||||||
chr11:117397966
|
T | C | 4 | a0009c0020t0014g0327a0009c0021t0019g0082a0013c0018t0014g0269others(1): Show | 4 | HG02559.hp1 HG03041.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3501+653T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117397966 | ||||||
chr11:117397967
|
T | C | 44 | a0001c0002t0001g0050a0001c0002t0001g0070a0001c0002t0001g0071others(41): Show | 50 | HG00099.hp1 HG00140.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.3501+654T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117397967 | ||||||
chr11:117398316
|
A | C | 4 | a0009c0020t0014g0327a0009c0021t0019g0082a0013c0018t0014g0269others(1): Show | 4 | HG02559.hp1 HG03041.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3501+1003A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117398316 | ||||||
chr11:117398375
|
T | C | 4 | a0001c0002t0002g0001a0001c0002t0002g0144a0001c0002t0002g0175others(1): Show | 7 | HG00544.hp2 HG02083.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.3501+1062T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117398375 | ||||||
chr11:117398526
|
C | T | 5 | a0002c0001t0009g0184a0002c0001t0009g0192a0002c0001t0009g0256others(2): Show | 5 | HG01074.hp1 HG01243.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.3501+1213C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117398526 | ||||||
chr11:117398553
|
T | A | 12 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(9): Show | 12 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.3501+1240T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117398553 | ||||||
chr11:117398585
|
C | CT | 12 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(9): Show | 12 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.3501+1274dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr11 | 117398585 | |||||
chr11:117398629
|
T | G | 1 | a0001c0005t0005g0173 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3501+1316T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117398629 | ||||||
chr11:117398640
|
G | A | 4 | a0009c0020t0014g0327a0009c0021t0019g0082a0013c0018t0014g0269others(1): Show | 4 | HG02559.hp1 HG03041.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3501+1327G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117398640 | ||||||
chr11:117399061
|
G | A | 5 | a0005c0006t0007g0048a0005c0006t0007g0049a0005c0006t0007g0075others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3501+1748G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117399061 | ||||||
chr11:117399107
|
G | A | 1 | a0001c0002t0005g0151 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3501+1794G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117399107 | ||||||
chr11:117399126
|
C | T | 4 | a0007c0010t0002g0167a0007c0010t0002g0168a0007c0010t0002g0174others(1): Show | 4 | HG01074.hp2 HG01081.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.3501+1813C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117399126 | ||||||
chr11:117399684
|
A | G | 1 | a0001c0002t0002g0171 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3501+2371A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117399684 | ||||||
chr11:117399746
|
CT | C | 10 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(7): Show | 10 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.3501+2442delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr11 | 117399746 | |||||
chr11:117399908
|
T | G | 1 | a0026c0035t0013g0046 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3501+2595T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117399908 | ||||||
chr11:117400102
|
A | C | 111 | a0001c0002t0003g0177a0002c0001t0001g0004a0002c0001t0001g0013others(108): Show | 122 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.3501+2789A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117400102 | ||||||
chr11:117400575
|
G | A | 4 | a0009c0020t0014g0327a0009c0021t0019g0082a0013c0018t0014g0269others(1): Show | 4 | HG02559.hp1 HG03041.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3501+3262G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117400575 | ||||||
chr11:117400713
|
G | A | 1 | a0002c0001t0003g0190 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3501+3400G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117400713 | ||||||
chr11:117400783
|
C | T | 326 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(323): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.3501+3470C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117400783 | ||||||
chr11:117401137
|
T | C | 1 | a0002c0001t0003g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3501+3824T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117401137 | ||||||
chr11:117401214
|
C | T | 2 | a0009c0020t0014g0327a0013c0018t0014g0269 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3501+3901C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117401214 | ||||||
chr11:117401290
|
T | C | 9 | a0006c0007t0006g0029a0006c0007t0006g0030a0006c0007t0006g0265others(6): Show | 9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.3501+3977T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117401290 | ||||||
chr11:117401531
|
G | T | 2 | a0009c0021t0019g0082a0023c0032t0020g0193 | 2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3501+4218G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117401531 | ||||||
chr11:117401970
|
C | G | 1 | a0001c0005t0005g0329 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3501+4657C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117401970 | ||||||
chr11:117402223
|
G | T | 93 | a0001c0013t0005g0236a0002c0001t0001g0013a0002c0001t0001g0014others(90): Show | 100 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.3501+4910G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402223 | ||||||
chr11:117402335
|
T | C | 330 | a0001c0002t0001g0037a0001c0002t0001g0040a0001c0002t0001g0041others(327): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.3501+5022T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402335 | ||||||
chr11:117402378
|
G | T | 6 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(3): Show | 6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.3501+5065G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402378 | ||||||
chr11:117402423
|
G | A | 3 | a0008c0011t0012g0080a0008c0011t0012g0081a0025c0029t0012g0079 | 3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3501+5110G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402423 | ||||||
chr11:117402437
|
T | C | 2 | a0009c0021t0019g0082a0023c0032t0020g0193 | 2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3501+5124T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402437 | ||||||
chr11:117402453
|
T | C | 3 | a0004c0034t0007g0039a0008c0011t0007g0028a0024c0030t0021g0038 | 3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3501+5140T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402453 | ||||||
chr11:117402467
|
G | T | 5 | a0002c0001t0003g0134a0002c0001t0003g0135a0002c0001t0003g0199others(2): Show | 5 | HG02809.hp1 HG03041.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.3501+5154G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402467 | ||||||
chr11:117402546
|
C | T | 4 | a0009c0020t0014g0327a0009c0021t0019g0082a0013c0018t0014g0269others(1): Show | 4 | HG02559.hp1 HG03041.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3501+5233C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402546 | ||||||
chr11:117402870
|
T | G | 1 | a0004c0004t0001g0310 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3502-5055T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402870 | ||||||
chr11:117402913
|
C | T | 1 | a0004c0004t0001g0295 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3502-5012C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402913 | ||||||
chr11:117402943
|
A | G | 6 | a0006c0007t0006g0265a0006c0007t0006g0267a0006c0007t0006g0270others(3): Show | 6 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.3502-4982A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402943 | ||||||
chr11:117402953
|
G | A | 4 | a0009c0020t0014g0327a0009c0021t0019g0082a0013c0018t0014g0269others(1): Show | 4 | HG02559.hp1 HG03041.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3502-4972G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402953 | ||||||
chr11:117403117
|
T | C | 2 | a0001c0002t0002g0088a0001c0002t0003g0177 | 2 | HG02027.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.3502-4808T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117403117 | ||||||
chr11:117403215
|
T | A | 1 | a0001c0002t0022g0343 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3502-4710T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117403215 | ||||||
chr11:117403283
|
G | A | 1 | a0005c0006t0007g0076 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3502-4642G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117403283 | ||||||
chr11:117403296
|
G | A | 1 | a0001c0002t0002g0348 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3502-4629G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117403296 | ||||||
chr11:117403312
|
G | T | 2 | a0009c0021t0019g0082a0023c0032t0020g0193 | 2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3502-4613G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117403312 | ||||||
chr11:117403805
|
T | A | 29 | a0002c0001t0003g0066a0002c0001t0003g0092a0002c0001t0003g0096others(26): Show | 29 | HG00408.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.3502-4120T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117403805 | ||||||
chr11:117404022
|
C | T | 1 | a0004c0004t0001g0289 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3502-3903C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117404022 | ||||||
chr11:117404114
|
G | C | 1 | a0009c0021t0019g0082 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3502-3811G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117404114 | ||||||
chr11:117404362
|
G | A | 2 | a0001c0002t0002g0153a0001c0002t0002g0169 | 2 | HG03669.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.3502-3563G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117404362 | ||||||
chr11:117404638
|
C | T | 1 | a0003c0022t0005g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3502-3287C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117404638 | ||||||
chr11:117404792
|
T | G | 5 | a0005c0006t0008g0045a0009c0020t0014g0327a0009c0021t0019g0082others(2): Show | 5 | HG02559.hp1 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3502-3133T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117404792 | ||||||
chr11:117404800
|
A | G | 1 | a0002c0001t0003g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3502-3125A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117404800 | ||||||
chr11:117404845
|
G | C | 137 | a0001c0005t0005g0329a0001c0005t0005g0331a0001c0005t0005g0355others(134): Show | 148 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.3502-3080G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117404845 | ||||||
chr11:117405099
|
G | A | 6 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(3): Show | 6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.3502-2826G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117405099 | ||||||
chr11:117405171
|
G | C | 93 | a0001c0005t0005g0329a0001c0005t0005g0331a0001c0005t0005g0355others(90): Show | 99 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.3502-2754G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117405171 | ||||||
chr11:117405795
|
C | G | 1 | a0001c0005t0005g0274 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3502-2130C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117405795 | ||||||
chr11:117405985
|
T | C | 1 | a0001c0002t0001g0050 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3502-1940T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117405985 | ||||||
chr11:117406067
|
T | G | 6 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(3): Show | 6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.3502-1858T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406067 | ||||||
chr11:117406086
|
C | T | 63 | a0001c0005t0005g0329a0001c0005t0005g0331a0001c0005t0005g0355others(60): Show | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.3502-1839C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406086 | ||||||
chr11:117406234
|
C | T | 1 | a0004c0004t0001g0293 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3502-1691C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406234 | ||||||
chr11:117406338
|
A | G | 9 | a0006c0007t0006g0029a0006c0007t0006g0030a0006c0007t0006g0265others(6): Show | 9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.3502-1587A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406338 | ||||||
chr11:117406517
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A | C | 1 | a0004c0004t0001g0332 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3502-1408A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406517 | ||||||
chr11:117406613
|
CGTACATG others(11): Show |
C | 1 | a0025c0029t0012g0079 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3502-1311_3502-129 others(22): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406613 | ||||||
chr11:117406637
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A | C | 1 | a0001c0002t0002g0314 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3502-1288A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406637 | ||||||
chr11:117406649
|
G | A | 4 | a0001c0002t0002g0001a0001c0002t0002g0144a0001c0002t0002g0175others(1): Show | 7 | HG00544.hp2 HG02083.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.3502-1276G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406649 | ||||||
chr11:117406869
|
G | A | 1 | a0001c0005t0005g0033 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3502-1056G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406869 | ||||||
chr11:117406934
|
A | G | 1 | a0001c0002t0001g0317 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3502-991A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406934 | ||||||
chr11:117407026
|
G | A | 1 | a0001c0005t0005g0085 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3502-899G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117407026 | ||||||
chr11:117407199
|
G | A | 2 | a0002c0001t0003g0187a0002c0001t0003g0188 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3502-726G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117407199 | ||||||
chr11:117407220
|
G | C | 2 | a0009c0020t0014g0327a0013c0018t0014g0269 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3502-705G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117407220 | ||||||
chr11:117407457
|
C | CA | 127 | a0001c0002t0001g0326a0001c0002t0002g0001a0001c0002t0002g0008others(124): Show | 136 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.3502-445dupA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr11 | 117407457 | |||||
chr11:117407457
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C | CAA | 21 | a0001c0002t0002g0147a0001c0002t0002g0164a0001c0002t0004g0157others(18): Show | 21 | HG00408.hp1 HG00597.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.3502-446_3502-445d others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr11 | 117407457 | |||||
chr11:117407457
|
CA | C | 75 | a0001c0002t0001g0040a0001c0002t0001g0071a0001c0005t0005g0329others(72): Show | 80 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.3502-445delA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr11 | 117407457 | |||||
chr11:117407504
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A | C | 1 | a0001c0005t0005g0274 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3502-421A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117407504 | ||||||
chr11:117407619
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C | T | 1 | a0004c0034t0007g0039 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3502-306C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117407619 | ||||||
chr11:117408056
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C | T | 1 | a0001c0002t0004g0157 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3609+24C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 28/32 | chr11 | 117408056 | ||||||
chr11:117408121
|
G | T | 2 | a0002c0001t0003g0134a0002c0001t0003g0135 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3609+89G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 28/32 | chr11 | 117408121 | ||||||
chr11:117408147
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A | G | 1 | a0009c0021t0019g0082 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3609+115A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 28/32 | chr11 | 117408147 | ||||||
chr11:117408251
|
G | GA | 6 | a0004c0009t0008g0021a0004c0009t0008g0022a0004c0009t0008g0023others(3): Show | 6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.3609+221dupA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr11 | 117408251 | |||||
chr11:117408380
|
C | T | 2 | a0001c0002t0002g0019a0001c0002t0002g0353 | 3 | NA18944.hp1 NA19007.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.3609+348C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 28/32 | chr11 | 117408380 | ||||||
chr11:117408849
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C | T | 1 | a0009c0021t0019g0082 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3610-41C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 28/32 | chr11 | 117408849 | ||||||
chr11:117409279
|
G | C | 1 | a0003c0022t0005g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3748+251G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 29/32 | chr11 | 117409279 | ||||||
chr11:117410008
|
TC | T | 65 | a0001c0002t0001g0326a0001c0002t0002g0001a0001c0002t0002g0008others(62): Show | 73 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.4096+45delC | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr11 | 117410008 | |||||
chr11:117410046
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T | C | 2 | a0004c0034t0007g0039a0024c0030t0021g0038 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.4096+81T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410046 | ||||||
chr11:117410064
|
C | G | 3 | a0008c0011t0012g0080a0008c0011t0012g0081a0025c0029t0012g0079 | 3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4096+99C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410064 | ||||||
chr11:117410277
|
C | T | 1 | a0001c0005t0005g0329 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.4096+312C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410277 | ||||||
chr11:117410332
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A | G | 9 | a0006c0007t0006g0029a0006c0007t0006g0030a0006c0007t0006g0265others(6): Show | 9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.4096+367A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410332 | ||||||
chr11:117410455
|
G | A | 1 | a0001c0005t0005g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4097-373G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410455 | ||||||
chr11:117410548
|
G | A | 27 | a0001c0002t0001g0050a0001c0002t0001g0070a0001c0002t0001g0071others(24): Show | 31 | HG01069.hp2 HG01123.hp2 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.4097-280G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410548 | ||||||
chr11:117410601
|
G | T | 1 | a0004c0004t0001g0067 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.4097-227G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410601 | ||||||
chr11:117410602
|
G | T | 1 | a0001c0002t0002g0340 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4097-226G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410602 | ||||||
chr11:117410641
|
C | T | 4 | a0009c0020t0014g0327a0009c0021t0019g0082a0013c0018t0014g0269others(1): Show | 4 | HG02559.hp1 HG03041.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.4097-187C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410641 | ||||||
chr11:117410759
|
G | A | 2 | a0009c0020t0014g0327a0013c0018t0014g0269 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4097-69G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410759 | ||||||
chr11:117410895
|
G | T | 1 | a0004c0034t0007g0039 | 1 | HG02145.hp2 | splice_donor_variant&intron_variant | HIGH | c.4163+1G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 31/32 | chr11 | 117410895 | ||||||
chr11:117411750
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C | T | 1 | a0001c0002t0002g0352 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.4164-45C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 31/32 | chr11 | 117411750 | ||||||
chr11:117411999
|
C | T | 1 | a0001c0002t0023g0242 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.4287-73C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 32/32 | chr11 | 117411999 | ||||||
chr11:117412026
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C | T | 70 | a0001c0002t0003g0177a0002c0001t0003g0002a0002c0001t0003g0011others(67): Show | 75 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.4287-46C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 32/32 | chr11 | 117412026 |