Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 80254 |
|---|---|
| ensemblid | ENSG00000182923.20 |
| hgncid | 25815 |
| symbol | CEP63 |
| name | centrosomal protein 63 |
| refseq_nuc | NM_001353108.3 |
| refseq_prot | NP_001340037.1 |
| ensembl_nuc | ENST00000675561.1 |
| ensembl_prot | ENSP00000502085.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 134486057 |
| end | 134565031 |
| strand | + |
| ver | v1.2 |
| region | chr3:134486057-134565031 |
| region5000 | chr3:134481057-134570031 |
| regionname0 | CEP63_chr3_134486057_134565031 |
| regionname5000 | CEP63_chr3_134481057_134570031 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 703 | 230 | 80 | 34 | 75 | 9 | 31 | 62 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0002 | 0/1 | 703 | 85 | 4 | 18 | 52 | 4 | 6 | 41 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0003 | 0/0 | 703 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0004 | 0/0 | 703 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0005 | 0/0 | 703 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0006 | 0/0 | 703 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0007 | 0/0 | 703 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0008 | 0/0 | 703 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2112 | 167 | 68 | 22 | 50 | 6 | 20 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| c0002 | 0/1 | 2112 | 82 | 4 | 18 | 49 | 4 | 6 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| c0003 | 0/0 | 2112 | 59 | 12 | 12 | 22 | 2 | 11 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| c0004 | 0/0 | 2112 | 3 | 0 | 0 | 3 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| c0005 | 0/0 | 2112 | 2 | 0 | 0 | 2 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| c0006 | 0/0 | 2112 | 2 | 1 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| c0007 | 0/0 | 2112 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| c0008 | 0/0 | 2112 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| c0009 | 0/0 | 2112 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| c0010 | 0/0 | 2112 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| c0011 | 0/0 | 2112 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| c0012 | 0/0 | 2112 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| c0013 | 0/0 | 2112 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3668 | 135 | 38 | 24 | 51 | 7 | 14 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0002 | 0/0 | 3668 | 57 | 18 | 10 | 24 | 1 | 4 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0003 | 0/0 | 3668 | 45 | 0 | 8 | 25 | 3 | 9 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0004 | 0/0 | 3668 | 25 | 0 | 0 | 17 | 1 | 7 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0005 | 0/0 | 3668 | 9 | 0 | 0 | 8 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0006 | 0/0 | 3668 | 8 | 2 | 4 | 0 | 2 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0007 | 0/0 | 3669 | 5 | 4 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0008 | 0/0 | 3668 | 4 | 0 | 2 | 0 | 0 | 2 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0009 | 0/0 | 3668 | 4 | 3 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0010 | 0/0 | 3668 | 3 | 3 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0011 | 0/0 | 3668 | 3 | 3 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0012 | 0/0 | 3668 | 3 | 2 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0013 | 1/0 | 3668 | 3 | 2 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0014 | 0/0 | 3668 | 2 | 1 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0015 | 0/0 | 3668 | 2 | 1 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0016 | 0/0 | 3668 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0017 | 0/0 | 3668 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0018 | 0/0 | 3668 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0019 | 0/0 | 3668 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0020 | 0/0 | 3668 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0021 | 0/0 | 3668 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0022 | 0/0 | 3668 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0023 | 0/0 | 3668 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0024 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0025 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0026 | 0/0 | 3683 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0027 | 0/0 | 3668 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0028 | 0/0 | 3668 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| t0029 | 0/0 | 3668 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0291 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2112 | 167 | 68 | 22 | 50 | 6 | 20 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0003 | 0/0 | 2112 | 59 | 12 | 12 | 22 | 2 | 11 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0004 | 0/0 | 2112 | 3 | 0 | 0 | 3 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0010 | 0/0 | 2112 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0002c0002 | 0/1 | 2112 | 82 | 4 | 18 | 49 | 4 | 6 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0002c0005 | 0/0 | 2112 | 2 | 0 | 0 | 2 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0002c0011 | 0/0 | 2112 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0003c0006 | 0/0 | 2112 | 2 | 1 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0004c0007 | 0/0 | 2112 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0005c0013 | 0/0 | 2112 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0006c0012 | 0/0 | 2112 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0007c0009 | 0/0 | 2112 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0008c0008 | 0/0 | 2112 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5779 | 36 | 21 | 4 | 1 | 2 | 8 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0002 | 0/0 | 5779 | 57 | 18 | 10 | 24 | 1 | 4 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0004 | 0/0 | 5779 | 25 | 0 | 0 | 17 | 1 | 7 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0005 | 0/0 | 5779 | 9 | 0 | 0 | 8 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0006 | 0/0 | 5779 | 8 | 2 | 4 | 0 | 2 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0007 | 0/0 | 5780 | 4 | 4 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0009 | 0/0 | 5779 | 4 | 3 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0010 | 0/0 | 5779 | 3 | 3 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0011 | 0/0 | 5779 | 3 | 3 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0012 | 0/0 | 5779 | 3 | 2 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0013 | 1/0 | 5779 | 3 | 2 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0014 | 0/0 | 5779 | 2 | 1 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0015 | 0/0 | 5779 | 2 | 1 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0017 | 0/0 | 5779 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0018 | 0/0 | 5779 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0019 | 0/0 | 5779 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0020 | 0/0 | 5779 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0021 | 0/0 | 5779 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0024 | 0/0 | 5780 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0025 | 0/0 | 5780 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0001t0029 | 0/0 | 5779 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0003t0001 | 0/0 | 5779 | 12 | 11 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0003t0003 | 0/0 | 5779 | 40 | 0 | 8 | 21 | 2 | 9 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0003t0008 | 0/0 | 5779 | 4 | 0 | 2 | 0 | 0 | 2 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0003t0023 | 0/0 | 5779 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0003t0027 | 0/0 | 5779 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0003t0028 | 0/0 | 5779 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0004t0003 | 0/0 | 5779 | 3 | 0 | 0 | 3 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0001c0010t0001 | 0/0 | 5779 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0002c0002t0001 | 0/1 | 5779 | 80 | 4 | 18 | 47 | 4 | 6 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0002c0002t0022 | 0/0 | 5779 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0002c0002t0026 | 0/0 | 5794 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0002c0005t0001 | 0/0 | 5779 | 2 | 0 | 0 | 2 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0002c0011t0001 | 0/0 | 5779 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0003c0006t0001 | 0/0 | 5779 | 2 | 1 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0004c0007t0003 | 0/0 | 5779 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0005c0013t0007 | 0/0 | 5780 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0006c0012t0016 | 0/0 | 5779 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0007c0009t0001 | 0/0 | 5779 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| a0008c0008t0003 | 0/0 | 5779 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | copy fasta | chr3 | 134481057 | 134570031 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0006g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0006g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0006g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0006g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0007g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0009g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0009g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0010g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0010g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0010g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0011g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0011g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0011g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0012g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0012g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0012g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0013g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0013g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0013g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0014g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0014g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0015g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0015g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0017g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0018g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0019g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0020g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0021g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0024g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0025g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0029g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0008g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0008g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0008g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0023g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0027g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0028g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0004t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0004t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0004t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0010t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0291 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0022g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0026g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0005t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0005t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0011t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0003c0006t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0003c0006t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0004c0007t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0005c0013t0007g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0006c0012t0016g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0007c0009t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0008c0008t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0095 | EUR | GBR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0272 | EUR | GBR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0287 | EUR | GBR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0084 | EUR | GBR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00280 | hp1 | a0004 | c0007 | t0003 | g0186 | EUR | FIN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0305 | EUR | FIN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0271 | EUR | FIN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00323 | hp2 | a0001 | c0010 | t0001 | g0290 | EUR | FIN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00423 | hp1 | a0001 | c0004 | t0003 | g0190 | EAS | CHS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | CHS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | CHS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | CHS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | CHS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | CHS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | CHS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00733 | hp1 | a0001 | c0003 | t0003 | g0155 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0214 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00735 | hp2 | a0001 | c0003 | t0027 | g0163 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0250 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0150 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01069 | hp1 | a0001 | c0003 | t0003 | g0204 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0269 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01081 | hp1 | a0001 | c0003 | t0003 | g0205 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0261 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0311 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01106 | hp1 | a0001 | c0003 | t0003 | g0172 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01106 | hp2 | a0001 | c0001 | t0014 | g0033 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01109 | hp1 | a0003 | c0006 | t0001 | g0222 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01109 | hp2 | a0005 | c0013 | t0007 | g0112 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0223 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01169 | hp1 | a0001 | c0001 | t0015 | g0144 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0073 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0213 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0273 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01192 | hp2 | a0001 | c0003 | t0003 | g0154 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0097 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0228 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01256 | hp2 | a0001 | c0003 | t0008 | g0007 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0298 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01258 | hp2 | a0001 | c0003 | t0008 | g0007 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0082 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0297 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0296 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0282 | EUR | IBS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01516 | hp2 | a0001 | c0003 | t0003 | g0187 | EUR | IBS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01884 | hp1 | a0001 | c0001 | t0013 | g0087 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0238 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0086 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01934 | hp1 | a0001 | c0003 | t0003 | g0169 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0252 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0005 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0226 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0227 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02015 | hp1 | a0001 | c0003 | t0003 | g0165 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0268 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02055 | hp2 | a0001 | c0001 | t0012 | g0105 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02056 | hp1 | a0001 | c0003 | t0003 | g0183 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02071 | hp2 | a0001 | c0003 | t0023 | g0173 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0118 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0251 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0072 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0134 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | CDX | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02155 | hp2 | a0001 | c0003 | t0003 | g0174 | EAS | CDX | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0143 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0091 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02273 | hp1 | a0001 | c0003 | t0003 | g0194 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0210 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0090 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02523 | hp1 | a0001 | c0003 | t0003 | g0191 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0116 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0099 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02602 | hp1 | a0001 | c0003 | t0003 | g0162 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0079 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02622 | hp1 | a0001 | c0001 | t0021 | g0108 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02630 | hp2 | a0001 | c0003 | t0028 | g0164 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02647 | hp1 | a0001 | c0001 | t0017 | g0034 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0096 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02683 | hp2 | a0001 | c0003 | t0003 | g0179 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0236 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02698 | hp2 | a0001 | c0003 | t0003 | g0197 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02717 | hp1 | a0001 | c0001 | t0024 | g0117 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0217 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02735 | hp2 | a0001 | c0003 | t0003 | g0160 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02738 | hp1 | a0001 | c0003 | t0008 | g0199 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02738 | hp2 | a0006 | c0012 | t0016 | g0093 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02818 | hp1 | a0001 | c0001 | t0025 | g0119 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02818 | hp2 | a0003 | c0006 | t0001 | g0220 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0032 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0312 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02976 | hp2 | a0001 | c0001 | t0011 | g0111 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0102 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0049 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0113 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0140 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03209 | hp1 | a0001 | c0001 | t0012 | g0106 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0141 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0283 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03453 | hp2 | a0001 | c0001 | t0013 | g0088 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0100 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0094 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03491 | hp2 | a0001 | c0003 | t0003 | g0170 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03492 | hp1 | a0001 | c0003 | t0003 | g0171 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0152 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0258 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0115 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0045 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03669 | hp2 | a0001 | c0003 | t0008 | g0180 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0121 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03704 | hp2 | a0001 | c0003 | t0003 | g0175 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0243 | SAS | BEB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03942 | hp1 | a0001 | c0003 | t0003 | g0177 | SAS | BEB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | BEB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0292 | SAS | STU | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | STU | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0038 | SAS | BEB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0280 | SAS | BEB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | STU | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0242 | SAS | STU | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG04204 | hp1 | a0001 | c0003 | t0003 | g0176 | SAS | STU | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0043 | SAS | STU | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | YRI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | CHB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | CHB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0114 | AFR | YRI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18940 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18947 | hp1 | a0008 | c0008 | t0003 | g0182 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18949 | hp2 | a0002 | c0005 | t0001 | g0159 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18950 | hp1 | a0002 | c0005 | t0001 | g0178 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18951 | hp1 | a0001 | c0003 | t0003 | g0181 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0126 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18962 | hp2 | a0001 | c0003 | t0003 | g0167 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18966 | hp2 | a0002 | c0002 | t0022 | g0246 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0124 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18969 | hp2 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18974 | hp2 | a0001 | c0003 | t0003 | g0156 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18978 | hp2 | a0001 | c0003 | t0003 | g0198 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18982 | hp1 | a0001 | c0003 | t0003 | g0196 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18984 | hp1 | a0001 | c0001 | t0005 | g0128 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18986 | hp2 | a0001 | c0003 | t0003 | g0188 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18988 | hp1 | a0001 | c0003 | t0003 | g0203 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18994 | hp2 | a0001 | c0003 | t0003 | g0189 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18998 | hp2 | a0001 | c0003 | t0003 | g0195 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18999 | hp1 | a0001 | c0003 | t0003 | g0185 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19000 | hp2 | a0001 | c0004 | t0003 | g0192 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19003 | hp2 | a0001 | c0003 | t0003 | g0157 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19010 | hp2 | a0001 | c0003 | t0003 | g0184 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19030 | hp1 | a0001 | c0001 | t0020 | g0092 | AFR | LWK | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0153 | AFR | LWK | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19043 | hp1 | a0001 | c0001 | t0029 | g0136 | AFR | LWK | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19043 | hp2 | a0007 | c0009 | t0001 | g0135 | AFR | LWK | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19060 | hp1 | a0002 | c0011 | t0001 | g0294 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19065 | hp1 | a0001 | c0003 | t0003 | g0158 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19076 | hp1 | a0001 | c0003 | t0003 | g0200 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19082 | hp1 | a0001 | c0003 | t0003 | g0166 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19082 | hp2 | a0002 | c0002 | t0026 | g0304 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19083 | hp2 | a0001 | c0004 | t0003 | g0193 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19085 | hp1 | a0001 | c0003 | t0003 | g0202 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0127 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19091 | hp2 | a0001 | c0003 | t0003 | g0201 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | YRI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0146 | AFR | YRI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA20129 | hp1 | a0001 | c0001 | t0018 | g0030 | AFR | ASW | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0147 | AFR | ASW | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0245 | EUR | TSI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA20752 | hp2 | a0001 | c0001 | t0006 | g0080 | EUR | TSI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0081 | EUR | TSI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA20805 | hp2 | a0001 | c0003 | t0003 | g0161 | EUR | TSI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01123 | hp1 | a0001 | c0003 | t0003 | g0168 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01123 | hp2 | a0001 | c0001 | t0012 | g0107 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02109 | hp1 | a0001 | c0001 | t0019 | g0061 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0098 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02559 | hp2 | a0001 | c0001 | t0011 | g0109 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG06807 | hp1 | a0001 | c0001 | t0011 | g0110 | AFR | USA | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG06807 | hp2 | a0001 | c0001 | t0015 | g0145 | AFR | USA | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | USA | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | USA | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0151 | AFR | LWK | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0270 | AFR | LWK | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0291 | REF | REF | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0013 | g0048 | REF | REF | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:134537268
|
G | C | 1 | a0004 | 1 | HG00280.hp1 | missense_variant&splice_region_variant | MODERATE | c.555G>C | p.Gln185His | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/15 | 726/5779 | 555/2112 | 185/703 | chr3 | 134537268 | ||
| chr3:134546264
|
C | G | 1 | a0005 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.905C>G | p.Thr302Ser | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/15 | 1076/5779 | 905/2112 | 302/703 | chr3 | 134546264 | ||
| chr3:134549149
|
C | A | 1 | a0003 | 2 | HG01109.hp1 HG02818.hp2 |
missense_variant | MODERATE | c.1155C>A | p.Asn385Lys | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/15 | 1326/5779 | 1155/2112 | 385/703 | chr3 | 134549149 | ||
| chr3:134550200
|
C | A | 1 | a0008 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.1320C>A | p.Asp440Glu | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/15 | 1491/5779 | 1320/2112 | 440/703 | chr3 | 134550200 | ||
| chr3:134559181
|
A | T | 1 | a0007 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1705A>T | p.Ile569Leu | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/15 | 1876/5779 | 1705/2112 | 569/703 | chr3 | 134559181 | ||
| chr3:134559308
|
C | T | 1 | a0006 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.1832C>T | p.Ser611Phe | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/15 | 2003/5779 | 1832/2112 | 611/703 | chr3 | 134559308 | ||
| chr3:134559428
|
C | T | 1 | a0002 | 85 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
missense_variant&splice_region_variant | MODERATE | c.1952C>T | p.Ser651Leu | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/15 | 2123/5779 | 1952/2112 | 651/703 | chr3 | 134559428 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:134507127
|
T | C | 6 | a0001c0003a0001c0004a0002c0005others(3): Show | 67 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(64): Show |
synonymous_variant | LOW | c.63T>C | p.Cys21Cys | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/15 | 234/5779 | 63/2112 | 21/703 | chr3 | 134507127 | ||
| chr3:134545597
|
C | A | 1 | a0001c0004 | 3 | HG00423.hp1 NA19000.hp2 NA19083.hp2 |
synonymous_variant | LOW | c.567C>A | p.Val189Val | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/15 | 738/5779 | 567/2112 | 189/703 | chr3 | 134545597 | ||
| chr3:134547380
|
G | A | 1 | a0001c0010 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.975G>A | p.Gly325Gly | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/15 | 1146/5779 | 975/2112 | 325/703 | chr3 | 134547380 | ||
| chr3:134550146
|
G | A | 1 | a0002c0011 | 1 | NA19060.hp1 | synonymous_variant | LOW | c.1266G>A | p.Gln422Gln | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/15 | 1437/5779 | 1266/2112 | 422/703 | chr3 | 134550146 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:134486068
|
C | T | 1 | a0001c0001t0029 | 1 | NA19043.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-160C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/15 | chr3 | 134486068 | ||||||
| chr3:134486144
|
C | G | 1 | a0001c0001t0009 | 4 | HG01243.hp1 HG02559.hp1 HG02572.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-84C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/15 | 9177 | chr3 | 134486144 | |||||
| chr3:134561553
|
T | A | 39 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(36): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*18T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 18 | chr3 | 134561553 | |||||
| chr3:134561696
|
A | G | 2 | a0001c0003t0027a0001c0003t0028 | 2 | HG00735.hp2 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*161A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 161 | chr3 | 134561696 | |||||
| chr3:134561943
|
TACCTGGA others(7): Show |
T | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*411_*424delCTGGAT others(8): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 411 | INFO_REALIGN_3_PRIME | chr3 | 134561943 | ||||
| chr3:134562055
|
A | T | 1 | a0001c0003t0028 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*520A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 520 | chr3 | 134562055 | |||||
| chr3:134562076
|
C | CT | 4 | a0001c0001t0007a0001c0001t0024a0001c0001t0025others(1): Show | 7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*542dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 543 | INFO_REALIGN_3_PRIME | chr3 | 134562076 | ||||
| chr3:134562106
|
G | T | 27 | a0001c0001t0001a0001c0001t0007a0001c0001t0009others(24): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*571G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 571 | chr3 | 134562106 | |||||
| chr3:134562193
|
A | G | 1 | a0001c0003t0023 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*658A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 658 | chr3 | 134562193 | |||||
| chr3:134562232
|
G | A | 1 | a0006c0012t0016 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*697G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 697 | chr3 | 134562232 | |||||
| chr3:134562409
|
T | A | 2 | a0001c0001t0014a0001c0001t0017 | 3 | HG01106.hp2 HG02647.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*874T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 874 | chr3 | 134562409 | |||||
| chr3:134562500
|
C | T | 1 | a0001c0001t0025 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*965C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 965 | chr3 | 134562500 | |||||
| chr3:134562689
|
C | T | 1 | a0001c0001t0006 | 8 | HG01175.hp1 HG01261.hp1 HG01346.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1154C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 1154 | chr3 | 134562689 | |||||
| chr3:134562884
|
C | T | 4 | a0001c0001t0007a0001c0001t0024a0001c0001t0025others(1): Show | 7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1349C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 1349 | chr3 | 134562884 | |||||
| chr3:134562977
|
T | C | 1 | a0001c0001t0018 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1442T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 1442 | chr3 | 134562977 | |||||
| chr3:134563020
|
C | T | 8 | a0001c0003t0003a0001c0003t0008a0001c0003t0023others(5): Show | 52 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1485C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 1485 | chr3 | 134563020 | |||||
| chr3:134563035
|
G | A | 1 | a0001c0001t0017 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1500G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 1500 | chr3 | 134563035 | |||||
| chr3:134563046
|
T | C | 2 | a0001c0001t0014a0001c0001t0017 | 3 | HG01106.hp2 HG02647.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1511T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 1511 | chr3 | 134563046 | |||||
| chr3:134563139
|
A | T | 1 | a0001c0001t0015 | 2 | HG01169.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1604A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 1604 | chr3 | 134563139 | |||||
| chr3:134563169
|
T | C | 1 | a0001c0001t0010 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1634T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 1634 | chr3 | 134563169 | |||||
| chr3:134563437
|
T | G | 27 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(24): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*1902T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 1902 | chr3 | 134563437 | |||||
| chr3:134563564
|
A | G | 8 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(5): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*2029A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2029 | chr3 | 134563564 | |||||
| chr3:134563642
|
C | T | 2 | a0001c0001t0010a0001c0001t0024 | 4 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2107C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2107 | chr3 | 134563642 | |||||
| chr3:134563914
|
T | C | 1 | a0001c0003t0008 | 4 | HG01256.hp2 HG01258.hp2 HG02738.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2379T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2379 | chr3 | 134563914 | |||||
| chr3:134563954
|
C | G | 26 | a0001c0001t0001a0001c0001t0007a0001c0001t0009others(23): Show | 206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*2419C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2419 | chr3 | 134563954 | |||||
| chr3:134563963
|
C | G | 2 | a0001c0001t0012a0001c0001t0021 | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2428C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2428 | chr3 | 134563963 | |||||
| chr3:134564015
|
A | T | 1 | a0001c0001t0011 | 3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2480A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2480 | chr3 | 134564015 | |||||
| chr3:134564106
|
T | C | 2 | a0001c0001t0011a0001c0001t0019 | 4 | HG02109.hp1 HG02559.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2571T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2571 | chr3 | 134564106 | |||||
| chr3:134564337
|
A | C | 1 | a0001c0001t0004 | 25 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2802A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2802 | chr3 | 134564337 | |||||
| chr3:134564409
|
C | A | 1 | a0001c0001t0005 | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2874C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2874 | chr3 | 134564409 | |||||
| chr3:134564474
|
T | C | 1 | a0001c0001t0020 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2939T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2939 | chr3 | 134564474 | |||||
| chr3:134564576
|
G | GATGCTGG others(22): Show |
1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3044_*3045insCTGG others(25): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3045 | INFO_REALIGN_3_PRIME | chr3 | 134564576 | ||||
| chr3:134564582
|
A | T | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3047A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3047 | chr3 | 134564582 | |||||
| chr3:134564587
|
C | G | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3052C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3052 | chr3 | 134564587 | |||||
| chr3:134564590
|
C | T | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3055C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3055 | chr3 | 134564590 | |||||
| chr3:134564635
|
C | T | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3100C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3100 | chr3 | 134564635 | |||||
| chr3:134564642
|
G | T | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3107G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3107 | chr3 | 134564642 | |||||
| chr3:134564653
|
T | C | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3118T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3118 | chr3 | 134564653 | |||||
| chr3:134564670
|
T | G | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3135T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3135 | chr3 | 134564670 | |||||
| chr3:134564673
|
G | T | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3138G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3138 | chr3 | 134564673 | |||||
| chr3:134564674
|
A | G | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3139A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3139 | chr3 | 134564674 | |||||
| chr3:134564683
|
T | A | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3148T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3148 | chr3 | 134564683 | |||||
| chr3:134564686
|
A | C | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3151A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3151 | chr3 | 134564686 | |||||
| chr3:134564693
|
A | G | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3158A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3158 | chr3 | 134564693 | |||||
| chr3:134564694
|
G | T | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3159G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3159 | chr3 | 134564694 | |||||
| chr3:134564706
|
T | C | 1 | a0001c0001t0012 | 3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3171T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3171 | chr3 | 134564706 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:134486207
|
C | T | 1 | a0001c0001t0002g0312 | 1 | HG02976.hp1 | splice_region_variant&intron_variant | LOW | c.-26+5C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134486207 | ||||||
| chr3:134486229
|
G | T | 211 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.-26+27G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134486229 | ||||||
| chr3:134486371
|
C | G | 1 | a0001c0001t0002g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-26+169C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134486371 | ||||||
| chr3:134486385
|
C | T | 212 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(209): Show | 217 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.-26+183C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134486385 | ||||||
| chr3:134486389
|
C | A | 212 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(209): Show | 217 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.-26+187C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134486389 | ||||||
| chr3:134486587
|
C | T | 1 | a0001c0001t0004g0102 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-26+385C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134486587 | ||||||
| chr3:134486603
|
ACCTT | A | 197 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(194): Show | 202 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.-26+406_-26+409del others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134486603 | |||||
| chr3:134486620
|
A | T | 1 | a0001c0001t0002g0101 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-26+418A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134486620 | ||||||
| chr3:134486970
|
G | C | 1 | a0001c0001t0002g0009 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-26+768G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134486970 | ||||||
| chr3:134487078
|
A | G | 192 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(189): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-26+876A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487078 | ||||||
| chr3:134487115
|
A | G | 3 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096 | 3 | HG00099.hp1 HG02683.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.-26+913A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487115 | ||||||
| chr3:134487207
|
G | C | 1 | a0001c0001t0002g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-26+1005G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487207 | ||||||
| chr3:134487227
|
A | G | 192 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(189): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-26+1025A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487227 | ||||||
| chr3:134487474
|
G | T | 1 | a0002c0002t0001g0311 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-26+1272G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487474 | ||||||
| chr3:134487569
|
A | G | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-26+1367A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487569 | ||||||
| chr3:134487574
|
A | G | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.-26+1372A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487574 | ||||||
| chr3:134487886
|
T | C | 206 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(203): Show | 211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.-26+1684T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487886 | ||||||
| chr3:134487907
|
T | C | 206 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(203): Show | 211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.-26+1705T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487907 | ||||||
| chr3:134487920
|
A | T | 2 | a0001c0001t0001g0309a0001c0001t0001g0310 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-26+1718A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487920 | ||||||
| chr3:134487954
|
A | G | 1 | a0006c0012t0016g0093 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-26+1752A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487954 | ||||||
| chr3:134488003
|
G | A | 215 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(212): Show | 220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.-26+1801G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488003 | ||||||
| chr3:134488151
|
C | T | 1 | a0002c0002t0001g0308 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-26+1949C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488151 | ||||||
| chr3:134488235
|
G | A | 192 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(189): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-26+2033G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488235 | ||||||
| chr3:134488274
|
T | C | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.-26+2072T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488274 | ||||||
| chr3:134488292
|
C | A | 84 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(81): Show | 86 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.-26+2090C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488292 | ||||||
| chr3:134488424
|
T | G | 7 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(4): Show | 7 | HG02630.hp1 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-26+2222T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488424 | ||||||
| chr3:134488616
|
A | G | 3 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307 | 3 | HG00280.hp2 HG00733.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.-26+2414A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488616 | ||||||
| chr3:134488745
|
G | A | 7 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(4): Show | 7 | HG01123.hp2 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-26+2543G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488745 | ||||||
| chr3:134488801
|
C | T | 3 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208 | 3 | HG01891.hp1 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-26+2599C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488801 | ||||||
| chr3:134488837
|
GTTAA | G | 7 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(4): Show | 7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-26+2640_-26+2643d others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134488837 | |||||
| chr3:134488844
|
A | T | 53 | a0001c0003t0003g0154a0001c0003t0003g0155a0001c0003t0003g0156others(50): Show | 54 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.-26+2642A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488844 | ||||||
| chr3:134488877
|
G | A | 5 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(2): Show | 5 | NA18941.hp2 NA18955.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26+2675G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488877 | ||||||
| chr3:134489158
|
C | CA | 20 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0002g0015others(17): Show | 20 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.-26+2978dupA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134489158 | |||||
| chr3:134489158
|
CA | C | 25 | a0001c0001t0004g0089a0001c0001t0005g0128a0001c0001t0007g0113others(22): Show | 25 | HG01069.hp1 HG01081.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.-26+2978delA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134489158 | |||||
| chr3:134489285
|
C | T | 1 | a0001c0001t0012g0105 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-26+3083C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134489285 | ||||||
| chr3:134489290
|
A | G | 206 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(203): Show | 211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.-26+3088A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134489290 | ||||||
| chr3:134489325
|
G | C | 212 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(209): Show | 217 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.-26+3123G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134489325 | ||||||
| chr3:134489377
|
G | T | 5 | a0001c0003t0001g0006a0001c0003t0001g0150a0001c0003t0001g0151others(2): Show | 6 | HG00741.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-26+3175G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134489377 | ||||||
| chr3:134489595
|
G | A | 1 | a0001c0001t0002g0018 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-26+3393G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134489595 | ||||||
| chr3:134489649
|
A | G | 2 | a0001c0001t0021g0108a0002c0002t0001g0303 | 2 | HG02622.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.-26+3447A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134489649 | ||||||
| chr3:134490010
|
A | C | 1 | a0001c0001t0001g0302 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-26+3808A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134490010 | ||||||
| chr3:134490021
|
C | A | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+3819C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134490021 | ||||||
| chr3:134490024
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0299a0001c0001t0001g0300others(1): Show | 5 | HG00609.hp2 HG03490.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-26+3822A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134490024 | ||||||
| chr3:134490183
|
A | T | 4 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111others(1): Show | 4 | HG02559.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+3981A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134490183 | ||||||
| chr3:134490193
|
C | G | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-26+3991C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134490193 | ||||||
| chr3:134490347
|
C | T | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+4145C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134490347 | ||||||
| chr3:134490407
|
T | G | 6 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(3): Show | 6 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26+4205T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134490407 | ||||||
| chr3:134490460
|
A | G | 2 | a0002c0002t0001g0297a0002c0002t0001g0298 | 2 | HG01258.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.-26+4258A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134490460 | ||||||
| chr3:134490575
|
G | GT | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.-26+4376dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134490575 | |||||
| chr3:134490647
|
T | TCCCATAA others(8): Show |
201 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(198): Show | 206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.-26+4458_-26+4472d others(17): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134490647 | |||||
| chr3:134490700
|
A | G | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-26+4498A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134490700 | ||||||
| chr3:134491114
|
A | G | 26 | a0001c0001t0002g0017a0001c0001t0002g0064a0001c0001t0002g0065others(23): Show | 27 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.-25-4182A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134491114 | ||||||
| chr3:134491156
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-25-4140A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134491156 | ||||||
| chr3:134491341
|
A | G | 203 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(200): Show | 208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.-25-3955A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134491341 | ||||||
| chr3:134491391
|
G | A | 1 | a0002c0002t0001g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-25-3905G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134491391 | ||||||
| chr3:134491407
|
A | G | 3 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111 | 3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-25-3889A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134491407 | ||||||
| chr3:134491544
|
A | G | 1 | a0005c0013t0007g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-25-3752A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134491544 | ||||||
| chr3:134491766
|
G | A | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25-3530G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134491766 | ||||||
| chr3:134491881
|
G | C | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-25-3415G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134491881 | ||||||
| chr3:134492070
|
C | CT | 187 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(184): Show | 192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-25-3205dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134492070 | |||||
| chr3:134492070
|
C | CTT | 19 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0005g0121others(16): Show | 19 | HG02738.hp1 HG02809.hp1 HG02818.hp1 others(16): Show |
intron_variant | MODIFIER | c.-25-3206_-25-3205d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134492070 | |||||
| chr3:134492070
|
CT | C | 10 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0004g0019others(7): Show | 10 | HG01168.hp2 HG01169.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-25-3205delT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134492070 | |||||
| chr3:134492077
|
T | C | 3 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111 | 3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-25-3219T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492077 | ||||||
| chr3:134492166
|
C | T | 2 | a0001c0001t0013g0087a0001c0001t0013g0088 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-25-3130C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492166 | ||||||
| chr3:134492194
|
C | G | 203 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(200): Show | 208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.-25-3102C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492194 | ||||||
| chr3:134492211
|
C | T | 1 | a0005c0013t0007g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-25-3085C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492211 | ||||||
| chr3:134492222
|
C | T | 203 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(200): Show | 208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.-25-3074C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492222 | ||||||
| chr3:134492435
|
A | G | 4 | a0001c0001t0009g0097a0001c0001t0009g0098a0001c0001t0009g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-2861A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492435 | ||||||
| chr3:134492480
|
C | CTACT | 218 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(215): Show | 223 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-25-2816_-25-2815i others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492480 | ||||||
| chr3:134492572
|
CT | C | 17 | a0001c0001t0002g0015a0001c0001t0002g0021a0001c0001t0002g0022others(14): Show | 17 | HG00738.hp2 HG01891.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-25-2707delT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134492572 | |||||
| chr3:134492604
|
A | G | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.-25-2692A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492604 | ||||||
| chr3:134492807
|
C | T | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.-25-2489C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492807 | ||||||
| chr3:134492865
|
A | T | 3 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107 | 3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-25-2431A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492865 | ||||||
| chr3:134492998
|
C | T | 3 | a0001c0001t0013g0087a0001c0001t0013g0088a0001c0001t0020g0092 | 3 | HG01884.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-25-2298C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492998 | ||||||
| chr3:134493030
|
A | G | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-25-2266A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134493030 | ||||||
| chr3:134493173
|
C | T | 1 | a0001c0003t0003g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-25-2123C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134493173 | ||||||
| chr3:134493216
|
A | C | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25-2080A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134493216 | ||||||
| chr3:134493275
|
C | T | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-25-2021C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134493275 | ||||||
| chr3:134493284
|
G | A | 1 | a0001c0001t0024g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-25-2012G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134493284 | ||||||
| chr3:134493614
|
A | C | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-1682A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134493614 | ||||||
| chr3:134493684
|
T | C | 218 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(215): Show | 223 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-25-1612T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134493684 | ||||||
| chr3:134493744
|
C | T | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25-1552C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134493744 | ||||||
| chr3:134494048
|
T | G | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-1248T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494048 | ||||||
| chr3:134494092
|
A | ATATT | 37 | a0001c0001t0002g0009a0001c0001t0002g0016a0001c0001t0002g0021others(34): Show | 38 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.-25-1166_-25-1163d others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134494092 | |||||
| chr3:134494092
|
A | ATATTTAT others(1): Show |
11 | a0001c0001t0002g0017a0001c0001t0002g0029a0001c0001t0002g0067others(8): Show | 11 | HG01175.hp1 HG02074.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-25-1170_-25-1163d others(10): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134494092 | |||||
| chr3:134494092
|
A | ATATTTAT others(5): Show |
1 | a0001c0001t0002g0066 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-25-1174_-25-1163d others(14): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134494092 | |||||
| chr3:134494092
|
A | T | 1 | a0001c0001t0002g0101 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-25-1204A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494092 | ||||||
| chr3:134494092
|
ATATT | A | 14 | a0001c0001t0001g0221a0001c0001t0001g0299a0001c0001t0009g0097others(11): Show | 14 | HG00609.hp2 HG01243.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.-25-1166_-25-1163d others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134494092 | |||||
| chr3:134494092
|
ATATTTAT others(1): Show |
A | 193 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(190): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-25-1170_-25-1163d others(10): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134494092 | |||||
| chr3:134494092
|
ATATTTAT others(13): Show |
A | 8 | a0001c0001t0005g0120a0001c0001t0005g0122a0001c0001t0005g0123others(5): Show | 8 | NA18940.hp2 NA18951.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25-1182_-25-1163d others(22): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134494092 | |||||
| chr3:134494201
|
C | T | 1 | a0001c0003t0003g0196 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-25-1095C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494201 | ||||||
| chr3:134494228
|
A | G | 211 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.-25-1068A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494228 | ||||||
| chr3:134494252
|
C | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-25-1044C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494252 | ||||||
| chr3:134494281
|
A | C | 1 | a0006c0012t0016g0093 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-25-1015A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494281 | ||||||
| chr3:134494281
|
AT | A | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25-1001delT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134494281 | |||||
| chr3:134494286
|
T | TC | 3 | a0001c0001t0001g0129a0001c0003t0027g0163a0001c0003t0028g0164 | 3 | HG00735.hp2 HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-25-1010_-25-1009i others(3): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494286 | ||||||
| chr3:134494338
|
ACTC | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0301 | 3 | HG03490.hp1 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-25-955_-25-953del others(3): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134494338 | |||||
| chr3:134494533
|
G | C | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-25-763G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494533 | ||||||
| chr3:134494614
|
A | G | 2 | a0001c0001t0002g0022a0001c0001t0002g0028 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-25-682A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494614 | ||||||
| chr3:134494696
|
C | T | 221 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(218): Show | 226 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.-25-600C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494696 | ||||||
| chr3:134494714
|
G | A | 1 | a0001c0001t0004g0040 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-25-582G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494714 | ||||||
| chr3:134494823
|
A | G | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.-25-473A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494823 | ||||||
| chr3:134494869
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-25-427C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494869 | ||||||
| chr3:134495055
|
T | G | 287 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(284): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.-25-241T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134495055 | ||||||
| chr3:134495077
|
C | T | 1 | a0001c0003t0003g0195 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-25-219C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134495077 | ||||||
| chr3:134495078
|
G | A | 7 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(4): Show | 7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-25-218G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134495078 | ||||||
| chr3:134495090
|
T | A | 1 | a0001c0003t0003g0165 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-25-206T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134495090 | ||||||
| chr3:134495095
|
A | C | 10 | a0001c0001t0004g0001a0001c0001t0004g0019a0001c0001t0004g0020others(7): Show | 12 | HG00558.hp1 HG02083.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.-25-201A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134495095 | ||||||
| chr3:134495124
|
T | A | 1 | a0001c0001t0001g0302 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-25-172T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134495124 | ||||||
| chr3:134495139
|
T | C | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.-25-157T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134495139 | ||||||
| chr3:134495200
|
T | C | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.-25-96T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134495200 | ||||||
| chr3:134495732
|
C | G | 1 | a0001c0001t0002g0060 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.44+368C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134495732 | ||||||
| chr3:134495879
|
A | G | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+515A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134495879 | ||||||
| chr3:134496080
|
A | T | 1 | a0001c0001t0002g0060 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.44+716A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134496080 | ||||||
| chr3:134496174
|
A | G | 7 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(4): Show | 7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.44+810A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134496174 | ||||||
| chr3:134496199
|
A | AT | 191 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(188): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.44+838dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134496199 | |||||
| chr3:134496210
|
A | G | 191 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(188): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.44+846A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134496210 | ||||||
| chr3:134496431
|
A | AG | 58 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0010others(55): Show | 61 | HG00140.hp2 HG00738.hp2 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.44+1078dupG | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134496431 | |||||
| chr3:134496431
|
AG | A | 24 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(21): Show | 24 | HG01109.hp2 HG01123.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.44+1078delG | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134496431 | |||||
| chr3:134496431
|
AGG | A | 187 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(184): Show | 192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.44+1077_44+1078del others(2): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134496431 | |||||
| chr3:134496434
|
G | C | 3 | a0001c0001t0013g0087a0001c0001t0013g0088a0001c0001t0020g0092 | 3 | HG01884.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.44+1070G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134496434 | ||||||
| chr3:134496440
|
G | C | 7 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(4): Show | 7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.44+1076G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134496440 | ||||||
| chr3:134496441
|
G | A | 2 | a0001c0001t0013g0087a0001c0001t0013g0088 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.44+1077G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134496441 | ||||||
| chr3:134496607
|
G | T | 4 | a0001c0003t0003g0191a0001c0004t0003g0190a0001c0004t0003g0192others(1): Show | 4 | HG00423.hp1 HG02523.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.44+1243G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134496607 | ||||||
| chr3:134496632
|
A | G | 1 | a0002c0002t0001g0298 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.44+1268A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134496632 | ||||||
| chr3:134496651
|
A | G | 1 | a0002c0002t0001g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.44+1287A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134496651 | ||||||
| chr3:134496922
|
A | AT | 3 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107 | 3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.44+1559dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134496922 | |||||
| chr3:134496923
|
T | TC | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+1566dupC | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134496923 | |||||
| chr3:134497029
|
C | T | 1 | a0001c0001t0002g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.44+1665C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497029 | ||||||
| chr3:134497139
|
G | A | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.44+1775G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497139 | ||||||
| chr3:134497297
|
G | T | 218 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(215): Show | 223 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.44+1933G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497297 | ||||||
| chr3:134497367
|
A | G | 7 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(4): Show | 7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.44+2003A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497367 | ||||||
| chr3:134497479
|
C | T | 1 | a0001c0001t0004g0295 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.44+2115C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497479 | ||||||
| chr3:134497496
|
C | G | 3 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208 | 3 | HG01891.hp1 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.44+2132C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497496 | ||||||
| chr3:134497511
|
A | G | 1 | a0001c0001t0002g0018 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.44+2147A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497511 | ||||||
| chr3:134497555
|
A | C | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.44+2191A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497555 | ||||||
| chr3:134497739
|
A | ATT | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+2384_44+2385dup others(2): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134497739 | |||||
| chr3:134497801
|
A | G | 14 | a0001c0001t0001g0008a0001c0001t0001g0216a0001c0001t0001g0286others(11): Show | 15 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.44+2437A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497801 | ||||||
| chr3:134497835
|
C | G | 7 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(4): Show | 7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.44+2471C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497835 | ||||||
| chr3:134497933
|
G | A | 7 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.44+2569G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497933 | ||||||
| chr3:134498066
|
G | A | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.44+2702G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134498066 | ||||||
| chr3:134498230
|
C | T | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.44+2866C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134498230 | ||||||
| chr3:134498555
|
C | G | 1 | a0001c0001t0015g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.44+3191C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134498555 | ||||||
| chr3:134498683
|
C | T | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+3319C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134498683 | ||||||
| chr3:134499051
|
T | C | 1 | a0003c0006t0001g0222 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.44+3687T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499051 | ||||||
| chr3:134499062
|
A | G | 14 | a0001c0001t0001g0008a0001c0001t0001g0216a0001c0001t0001g0286others(11): Show | 15 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.44+3698A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499062 | ||||||
| chr3:134499076
|
C | T | 2 | a0002c0002t0001g0297a0002c0002t0001g0298 | 2 | HG01258.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.44+3712C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499076 | ||||||
| chr3:134499110
|
T | C | 4 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.44+3746T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499110 | ||||||
| chr3:134499316
|
A | C | 1 | a0001c0001t0002g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.44+3952A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499316 | ||||||
| chr3:134499320
|
T | G | 3 | a0001c0001t0013g0087a0001c0001t0013g0088a0001c0001t0020g0092 | 3 | HG01884.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.44+3956T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499320 | ||||||
| chr3:134499622
|
G | T | 3 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111 | 3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.44+4258G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499622 | ||||||
| chr3:134499711
|
A | G | 3 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111 | 3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.44+4347A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499711 | ||||||
| chr3:134499715
|
T | C | 218 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(215): Show | 223 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.44+4351T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499715 | ||||||
| chr3:134499820
|
C | CT | 20 | a0001c0001t0001g0139a0001c0001t0002g0009a0001c0001t0004g0295others(17): Show | 20 | HG01123.hp2 HG01168.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.44+4477dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134499820 | |||||
| chr3:134499820
|
C | CTT | 159 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(156): Show | 163 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.44+4476_44+4477dup others(2): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134499820 | |||||
| chr3:134499820
|
C | CTTT | 29 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0216others(26): Show | 30 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.44+4475_44+4477dup others(3): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134499820 | |||||
| chr3:134499820
|
CT | C | 19 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0022others(16): Show | 19 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.44+4477delT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134499820 | |||||
| chr3:134499855
|
G | A | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.44+4491G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499855 | ||||||
| chr3:134499961
|
T | C | 2 | a0001c0001t0002g0029a0001c0001t0018g0030 | 2 | NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.44+4597T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499961 | ||||||
| chr3:134500024
|
C | T | 1 | a0001c0001t0004g0020 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.44+4660C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500024 | ||||||
| chr3:134500031
|
G | T | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.44+4667G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500031 | ||||||
| chr3:134500045
|
C | T | 1 | a0001c0001t0002g0016 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.44+4681C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500045 | ||||||
| chr3:134500103
|
G | A | 1 | a0001c0003t0001g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.44+4739G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500103 | ||||||
| chr3:134500150
|
G | A | 2 | a0001c0001t0013g0087a0001c0001t0013g0088 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.44+4786G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500150 | ||||||
| chr3:134500159
|
A | G | 191 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(188): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.44+4795A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500159 | ||||||
| chr3:134500177
|
C | T | 221 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(218): Show | 226 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.44+4813C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500177 | ||||||
| chr3:134500292
|
T | C | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.44+4928T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500292 | ||||||
| chr3:134500332
|
C | T | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+4968C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500332 | ||||||
| chr3:134500335
|
G | A | 287 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(284): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.44+4971G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500335 | ||||||
| chr3:134500398
|
ACATGTGA others(3): Show |
A | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+5041_44+5050del others(10): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134500398 | |||||
| chr3:134500444
|
C | T | 1 | a0001c0001t0002g0017 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.44+5080C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500444 | ||||||
| chr3:134500477
|
G | A | 2 | a0002c0002t0001g0224a0002c0002t0001g0225 | 2 | HG00544.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.44+5113G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500477 | ||||||
| chr3:134500482
|
G | A | 1 | a0001c0001t0002g0029 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.44+5118G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500482 | ||||||
| chr3:134500506
|
T | C | 26 | a0001c0001t0002g0017a0001c0001t0002g0064a0001c0001t0002g0065others(23): Show | 27 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.44+5142T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500506 | ||||||
| chr3:134500805
|
GT | G | 5 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(2): Show | 5 | HG01109.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+5450delT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134500805 | |||||
| chr3:134500862
|
T | C | 2 | a0001c0001t0013g0087a0001c0001t0013g0088 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.44+5498T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500862 | ||||||
| chr3:134500977
|
T | TA | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.44+5614dupA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134500977 | |||||
| chr3:134501016
|
A | T | 5 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(2): Show | 5 | HG01109.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+5652A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501016 | ||||||
| chr3:134501151
|
C | T | 211 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.44+5787C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501151 | ||||||
| chr3:134501182
|
T | C | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.44+5818T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501182 | ||||||
| chr3:134501216
|
A | G | 7 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.44+5852A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501216 | ||||||
| chr3:134501277
|
C | G | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-5832C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501277 | ||||||
| chr3:134501284
|
C | T | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.45-5825C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501284 | ||||||
| chr3:134501405
|
A | G | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.45-5704A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501405 | ||||||
| chr3:134501479
|
A | T | 1 | a0004c0007t0003g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.45-5630A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501479 | ||||||
| chr3:134501570
|
A | AT | 213 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0131others(210): Show | 218 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.45-5530dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134501570 | |||||
| chr3:134501954
|
T | C | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-5155T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501954 | ||||||
| chr3:134501997
|
G | A | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-5112G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501997 | ||||||
| chr3:134502024
|
G | A | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-5085G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134502024 | ||||||
| chr3:134502163
|
G | T | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-4946G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134502163 | ||||||
| chr3:134502283
|
G | GT | 95 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(92): Show | 97 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.45-4817dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134502283 | |||||
| chr3:134502401
|
A | G | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-4708A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134502401 | ||||||
| chr3:134502597
|
C | G | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-4512C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134502597 | ||||||
| chr3:134502960
|
A | G | 3 | a0001c0001t0001g0216a0001c0001t0001g0289a0001c0010t0001g0290 | 3 | HG00323.hp2 HG02300.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.45-4149A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134502960 | ||||||
| chr3:134502981
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.45-4128A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134502981 | ||||||
| chr3:134503100
|
C | CT | 201 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(198): Show | 206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.45-3989dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134503100 | |||||
| chr3:134503100
|
C | CTT | 20 | a0001c0001t0002g0029a0001c0001t0005g0120a0001c0001t0005g0121others(17): Show | 20 | HG01884.hp1 HG02559.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.45-3990_45-3989dup others(2): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134503100 | |||||
| chr3:134503130
|
C | T | 3 | a0001c0001t0013g0087a0001c0001t0013g0088a0001c0001t0020g0092 | 3 | HG01884.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.45-3979C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503130 | ||||||
| chr3:134503250
|
C | A | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-3859C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503250 | ||||||
| chr3:134503294
|
C | T | 211 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.45-3815C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503294 | ||||||
| chr3:134503319
|
A | C | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.45-3790A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503319 | ||||||
| chr3:134503437
|
G | T | 1 | a0001c0001t0024g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.45-3672G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503437 | ||||||
| chr3:134503526
|
G | C | 1 | a0001c0003t0001g0146 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.45-3583G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503526 | ||||||
| chr3:134503604
|
T | G | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-3505T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503604 | ||||||
| chr3:134503665
|
G | T | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.45-3444G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503665 | ||||||
| chr3:134503739
|
C | A | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-3370C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503739 | ||||||
| chr3:134503840
|
G | GTTTCATT others(14): Show |
1 | a0001c0001t0021g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.45-3265_45-3264ins others(21): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134503840 | |||||
| chr3:134503840
|
G | GTTTCCAT others(15): Show |
201 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(198): Show | 206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.45-3264_45-3263ins others(22): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134503840 | |||||
| chr3:134503869
|
C | T | 1 | a0002c0002t0001g0285 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.45-3240C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503869 | ||||||
| chr3:134503880
|
A | G | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.45-3229A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503880 | ||||||
| chr3:134504003
|
G | C | 1 | a0001c0003t0001g0146 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.45-3106G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504003 | ||||||
| chr3:134504113
|
CT | C | 83 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(80): Show | 85 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.45-2984delT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134504113 | |||||
| chr3:134504115
|
T | C | 1 | a0001c0001t0013g0088 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.45-2994T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504115 | ||||||
| chr3:134504127
|
G | A | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-2982G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504127 | ||||||
| chr3:134504160
|
T | G | 1 | a0002c0002t0001g0298 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.45-2949T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504160 | ||||||
| chr3:134504169
|
C | G | 218 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(215): Show | 223 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.45-2940C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504169 | ||||||
| chr3:134504176
|
G | C | 218 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(215): Show | 223 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.45-2933G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504176 | ||||||
| chr3:134504208
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.45-2901G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504208 | ||||||
| chr3:134504256
|
A | AT | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.45-2847dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134504256 | |||||
| chr3:134504375
|
C | G | 26 | a0001c0001t0002g0017a0001c0001t0002g0064a0001c0001t0002g0065others(23): Show | 27 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.45-2734C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504375 | ||||||
| chr3:134504453
|
A | G | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.45-2656A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504453 | ||||||
| chr3:134504457
|
G | C | 1 | a0001c0003t0003g0167 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.45-2652G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504457 | ||||||
| chr3:134504475
|
A | G | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-2634A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504475 | ||||||
| chr3:134504594
|
G | A | 4 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(1): Show | 4 | HG02572.hp1 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.45-2515G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504594 | ||||||
| chr3:134504706
|
G | GC | 211 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.45-2401dupC | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134504706 | |||||
| chr3:134504721
|
G | A | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.45-2388G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504721 | ||||||
| chr3:134504766
|
C | G | 4 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.45-2343C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504766 | ||||||
| chr3:134504846
|
C | G | 1 | a0002c0002t0001g0275 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.45-2263C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504846 | ||||||
| chr3:134504888
|
T | C | 211 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.45-2221T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504888 | ||||||
| chr3:134504966
|
C | G | 11 | a0001c0001t0002g0074a0001c0001t0002g0083a0001c0001t0002g0084others(8): Show | 12 | HG00140.hp2 HG01099.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.45-2143C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504966 | ||||||
| chr3:134505023
|
C | T | 3 | a0001c0001t0004g0039a0001c0001t0013g0087a0001c0001t0013g0088 | 3 | HG01884.hp1 HG02155.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.45-2086C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505023 | ||||||
| chr3:134505076
|
A | T | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.45-2033A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505076 | ||||||
| chr3:134505264
|
T | A | 10 | a0002c0002t0001g0103a0002c0002t0001g0210a0002c0002t0001g0227others(7): Show | 10 | HG00558.hp2 HG01255.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.45-1845T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505264 | ||||||
| chr3:134505322
|
G | A | 2 | a0001c0003t0003g0188a0001c0003t0003g0195 | 2 | NA18986.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.45-1787G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505322 | ||||||
| chr3:134505330
|
T | G | 1 | a0002c0002t0001g0235 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.45-1779T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505330 | ||||||
| chr3:134505395
|
G | A | 5 | a0001c0003t0003g0154a0001c0003t0003g0155a0001c0003t0003g0168others(2): Show | 5 | HG00733.hp1 HG01123.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.45-1714G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505395 | ||||||
| chr3:134505399
|
G | C | 5 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(2): Show | 5 | NA18941.hp2 NA18955.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-1710G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505399 | ||||||
| chr3:134505551
|
C | T | 1 | a0002c0002t0001g0274 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.45-1558C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505551 | ||||||
| chr3:134505595
|
G | A | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45-1514G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505595 | ||||||
| chr3:134505595
|
G | C | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.45-1514G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505595 | ||||||
| chr3:134505659
|
T | C | 1 | a0002c0002t0001g0236 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.45-1450T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505659 | ||||||
| chr3:134505966
|
C | T | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-1143C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505966 | ||||||
| chr3:134506060
|
T | C | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.45-1049T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134506060 | ||||||
| chr3:134506402
|
C | T | 3 | a0001c0001t0013g0087a0001c0001t0013g0088a0001c0001t0020g0092 | 3 | HG01884.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.45-707C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134506402 | ||||||
| chr3:134506564
|
G | T | 9 | a0002c0002t0001g0213a0002c0002t0001g0217a0002c0002t0001g0269others(6): Show | 9 | HG00099.hp2 HG00323.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.45-545G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134506564 | ||||||
| chr3:134506753
|
C | G | 1 | a0001c0003t0003g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.45-356C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134506753 | ||||||
| chr3:134506843
|
G | A | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.45-266G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134506843 | ||||||
| chr3:134506873
|
A | G | 263 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(260): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.45-236A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134506873 | ||||||
| chr3:134506918
|
C | CA | 36 | a0001c0001t0001g0142a0001c0001t0001g0286a0001c0001t0001g0309others(33): Show | 36 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.45-166dupA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134506918 | |||||
| chr3:134506918
|
CA | C | 20 | a0001c0001t0002g0076a0001c0001t0004g0001a0001c0001t0004g0039others(17): Show | 22 | HG01069.hp2 HG01109.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.45-166delA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134506918 | |||||
| chr3:134506918
|
CAA | C | 10 | a0001c0001t0004g0089a0001c0001t0005g0120a0001c0001t0005g0125others(7): Show | 10 | HG02109.hp1 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.45-167_45-166delAA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134506918 | |||||
| chr3:134507063
|
C | T | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.45-46C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134507063 | ||||||
| chr3:134507317
|
C | T | 211 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.222+31C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134507317 | ||||||
| chr3:134507636
|
C | T | 2 | a0001c0001t0002g0067a0001c0001t0002g0071 | 2 | NA18939.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.222+350C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134507636 | ||||||
| chr3:134507991
|
G | T | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.222+705G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134507991 | ||||||
| chr3:134508074
|
A | C | 1 | a0001c0001t0002g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.222+788A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134508074 | ||||||
| chr3:134508258
|
G | A | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.222+972G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134508258 | ||||||
| chr3:134508260
|
G | T | 1 | a0001c0001t0001g0216 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.222+974G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134508260 | ||||||
| chr3:134508410
|
C | A | 7 | a0001c0003t0003g0170a0001c0003t0003g0171a0001c0003t0003g0172others(4): Show | 7 | HG00280.hp1 HG01069.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.222+1124C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134508410 | ||||||
| chr3:134508450
|
A | G | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.222+1164A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134508450 | ||||||
| chr3:134508464
|
G | T | 7 | a0001c0003t0003g0170a0001c0003t0003g0171a0001c0003t0003g0172others(4): Show | 7 | HG00280.hp1 HG01069.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.222+1178G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134508464 | ||||||
| chr3:134508667
|
C | T | 1 | a0001c0003t0003g0183 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.222+1381C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134508667 | ||||||
| chr3:134508802
|
C | A | 1 | a0001c0003t0001g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+1516C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134508802 | ||||||
| chr3:134508971
|
C | CT | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.222+1698dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134508971 | |||||
| chr3:134509101
|
G | T | 1 | a0001c0001t0004g0049 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.222+1815G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134509101 | ||||||
| chr3:134509196
|
G | A | 1 | a0002c0002t0001g0223 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.222+1910G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134509196 | ||||||
| chr3:134509340
|
C | G | 16 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0021others(13): Show | 16 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.222+2054C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134509340 | ||||||
| chr3:134509357
|
G | A | 1 | a0001c0001t0006g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.222+2071G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134509357 | ||||||
| chr3:134509477
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.222+2191A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134509477 | ||||||
| chr3:134509691
|
C | A | 4 | a0001c0001t0009g0097a0001c0001t0009g0098a0001c0001t0009g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+2405C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134509691 | ||||||
| chr3:134509786
|
A | G | 191 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(188): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.222+2500A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134509786 | ||||||
| chr3:134509787
|
A | G | 2 | a0001c0001t0013g0087a0001c0001t0013g0088 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.222+2501A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134509787 | ||||||
| chr3:134509934
|
G | A | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.222+2648G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134509934 | ||||||
| chr3:134510131
|
T | C | 1 | a0001c0001t0004g0045 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.222+2845T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510131 | ||||||
| chr3:134510187
|
T | C | 11 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(8): Show | 11 | HG01169.hp1 HG02630.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+2901T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510187 | ||||||
| chr3:134510253
|
G | A | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.222+2967G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510253 | ||||||
| chr3:134510375
|
A | G | 5 | a0001c0003t0001g0006a0001c0003t0001g0150a0001c0003t0001g0151others(2): Show | 6 | HG00741.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+3089A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510375 | ||||||
| chr3:134510400
|
G | A | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.222+3114G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510400 | ||||||
| chr3:134510563
|
G | A | 2 | a0001c0001t0013g0087a0001c0001t0013g0088 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.222+3277G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510563 | ||||||
| chr3:134510570
|
C | T | 1 | a0001c0003t0003g0158 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.222+3284C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510570 | ||||||
| chr3:134510701
|
G | A | 3 | a0001c0001t0013g0087a0001c0001t0013g0088a0001c0001t0020g0092 | 3 | HG01884.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.222+3415G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510701 | ||||||
| chr3:134510794
|
C | CTGG | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+3509_222+3511d others(5): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134510794 | |||||
| chr3:134510830
|
G | T | 1 | a0001c0001t0002g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.222+3544G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510830 | ||||||
| chr3:134510898
|
C | G | 2 | a0002c0002t0001g0233a0002c0002t0001g0234 | 2 | NA18950.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.222+3612C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510898 | ||||||
| chr3:134510898
|
C | T | 2 | a0001c0001t0013g0087a0001c0001t0013g0088 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.222+3612C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510898 | ||||||
| chr3:134510973
|
A | AT | 210 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(207): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.222+3699dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134510973 | |||||
| chr3:134511024
|
C | G | 221 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(218): Show | 226 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.222+3738C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511024 | ||||||
| chr3:134511172
|
A | G | 2 | a0002c0002t0001g0212a0002c0002t0001g0267 | 2 | NA18965.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.222+3886A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511172 | ||||||
| chr3:134511324
|
T | C | 1 | a0002c0002t0001g0274 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.222+4038T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511324 | ||||||
| chr3:134511362
|
T | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.222+4076T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511362 | ||||||
| chr3:134511392
|
A | T | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.222+4106A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511392 | ||||||
| chr3:134511535
|
C | T | 1 | a0001c0001t0002g0059 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.222+4249C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511535 | ||||||
| chr3:134511604
|
C | T | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.222+4318C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511604 | ||||||
| chr3:134511662
|
T | C | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.222+4376T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511662 | ||||||
| chr3:134511704
|
G | C | 1 | a0001c0001t0002g0009 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.222+4418G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511704 | ||||||
| chr3:134511861
|
A | G | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.222+4575A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511861 | ||||||
| chr3:134511969
|
A | G | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.222+4683A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511969 | ||||||
| chr3:134512152
|
C | T | 1 | a0002c0002t0001g0226 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.222+4866C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134512152 | ||||||
| chr3:134512164
|
A | G | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG01496.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.222+4878A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134512164 | ||||||
| chr3:134512215
|
CTG | C | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+4932_222+4933d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134512215 | |||||
| chr3:134512223
|
A | G | 2 | a0001c0001t0001g0309a0001c0001t0001g0310 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.222+4937A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134512223 | ||||||
| chr3:134512409
|
T | C | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.222+5123T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134512409 | ||||||
| chr3:134512606
|
C | T | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG01496.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.222+5320C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134512606 | ||||||
| chr3:134512689
|
A | G | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.222+5403A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134512689 | ||||||
| chr3:134513088
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.222+5802C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513088 | ||||||
| chr3:134513281
|
A | G | 3 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111 | 3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.222+5995A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513281 | ||||||
| chr3:134513373
|
C | T | 2 | a0001c0001t0002g0101a0001c0001t0020g0092 | 2 | HG03654.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.222+6087C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513373 | ||||||
| chr3:134513412
|
T | C | 3 | a0002c0002t0001g0282a0002c0002t0001g0291a0002c0002t0001g0292 | 3 | HG01516.hp1 HG04115.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.222+6126T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513412 | ||||||
| chr3:134513486
|
A | T | 308 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(305): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.222+6200A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513486 | ||||||
| chr3:134513497
|
A | G | 84 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(81): Show | 86 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.222+6211A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513497 | ||||||
| chr3:134513508
|
A | G | 90 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(87): Show | 95 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.222+6222A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513508 | ||||||
| chr3:134513554
|
C | A | 309 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(306): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.222+6268C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513554 | ||||||
| chr3:134513586
|
CATT | C | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+6305_222+6307d others(5): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134513586 | |||||
| chr3:134513624
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.222+6338A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513624 | ||||||
| chr3:134513735
|
G | A | 1 | a0002c0002t0001g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.222+6449G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513735 | ||||||
| chr3:134513805
|
A | G | 6 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(3): Show | 6 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+6519A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513805 | ||||||
| chr3:134513825
|
A | G | 1 | a0006c0012t0016g0093 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.222+6539A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513825 | ||||||
| chr3:134513998
|
C | G | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.222+6712C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513998 | ||||||
| chr3:134514078
|
C | G | 191 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(188): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.222+6792C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134514078 | ||||||
| chr3:134514146
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.222+6860G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134514146 | ||||||
| chr3:134514250
|
A | G | 191 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(188): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.222+6964A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134514250 | ||||||
| chr3:134514307
|
A | G | 1 | a0001c0001t0014g0033 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.222+7021A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134514307 | ||||||
| chr3:134514396
|
G | T | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.222+7110G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134514396 | ||||||
| chr3:134514569
|
T | C | 1 | a0001c0001t0006g0072 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.222+7283T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134514569 | ||||||
| chr3:134514623
|
GA | G | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+7341delA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134514623 | |||||
| chr3:134514752
|
C | A | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+7466C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134514752 | ||||||
| chr3:134515503
|
C | T | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.222+8217C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134515503 | ||||||
| chr3:134515514
|
C | T | 308 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(305): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.222+8228C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134515514 | ||||||
| chr3:134515543
|
G | A | 2 | a0001c0003t0027g0163a0001c0003t0028g0164 | 2 | HG00735.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.222+8257G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134515543 | ||||||
| chr3:134515994
|
G | A | 3 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111 | 3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.222+8708G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134515994 | ||||||
| chr3:134516129
|
C | T | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.222+8843C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516129 | ||||||
| chr3:134516279
|
A | G | 1 | a0002c0002t0001g0273 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.222+8993A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516279 | ||||||
| chr3:134516319
|
G | A | 308 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(305): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.222+9033G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516319 | ||||||
| chr3:134516323
|
T | C | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.222+9037T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516323 | ||||||
| chr3:134516476
|
C | A | 1 | a0002c0002t0001g0237 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.222+9190C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516476 | ||||||
| chr3:134516503
|
G | A | 8 | a0001c0003t0001g0006a0001c0003t0001g0141a0001c0003t0001g0146others(5): Show | 9 | HG00741.hp1 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+9217G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516503 | ||||||
| chr3:134516749
|
C | T | 3 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107 | 3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.222+9463C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516749 | ||||||
| chr3:134516750
|
A | C | 14 | a0001c0001t0001g0008a0001c0001t0001g0216a0001c0001t0001g0286others(11): Show | 15 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.222+9464A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516750 | ||||||
| chr3:134516762
|
A | C | 12 | a0001c0001t0001g0211a0001c0001t0001g0221a0001c0001t0001g0263others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.222+9476A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516762 | ||||||
| chr3:134516884
|
C | T | 1 | a0002c0002t0001g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.222+9598C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516884 | ||||||
| chr3:134516948
|
A | G | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.222+9662A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516948 | ||||||
| chr3:134517128
|
G | C | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.222+9842G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134517128 | ||||||
| chr3:134517233
|
C | G | 1 | a0001c0001t0004g0044 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.222+9947C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134517233 | ||||||
| chr3:134517464
|
C | T | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.222+10178C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134517464 | ||||||
| chr3:134517602
|
C | T | 1 | a0005c0013t0007g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.222+10316C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134517602 | ||||||
| chr3:134517607
|
C | T | 81 | a0002c0002t0001g0002a0002c0002t0001g0103a0002c0002t0001g0209others(78): Show | 83 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.222+10321C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134517607 | ||||||
| chr3:134517617
|
G | A | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.222+10331G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134517617 | ||||||
| chr3:134518230
|
A | G | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+10944A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134518230 | ||||||
| chr3:134518261
|
C | T | 191 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(188): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.222+10975C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134518261 | ||||||
| chr3:134518354
|
A | G | 304 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(301): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.222+11068A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134518354 | ||||||
| chr3:134518395
|
C | T | 1 | a0001c0003t0003g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.222+11109C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134518395 | ||||||
| chr3:134518430
|
A | C | 304 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(301): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.222+11144A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134518430 | ||||||
| chr3:134518871
|
C | T | 1 | a0001c0001t0004g0295 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.222+11585C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134518871 | ||||||
| chr3:134518875
|
A | C | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.222+11589A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134518875 | ||||||
| chr3:134518915
|
G | GA | 5 | a0001c0001t0004g0044a0001c0001t0012g0105a0001c0001t0012g0106others(2): Show | 5 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+11635dupA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134518915 | |||||
| chr3:134518937
|
A | C | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+11651A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134518937 | ||||||
| chr3:134519024
|
A | AC | 11 | a0001c0001t0002g0058a0001c0001t0004g0044a0001c0001t0005g0120others(8): Show | 11 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.222+11745dupC | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134519024 | |||||
| chr3:134519158
|
C | T | 1 | a0002c0002t0001g0103 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.222+11872C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519158 | ||||||
| chr3:134519381
|
G | A | 6 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(3): Show | 6 | HG00738.hp2 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+12095G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519381 | ||||||
| chr3:134519392
|
C | T | 1 | a0001c0001t0004g0040 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.222+12106C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519392 | ||||||
| chr3:134519425
|
C | T | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.222+12139C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519425 | ||||||
| chr3:134519430
|
G | A | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.222+12144G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519430 | ||||||
| chr3:134519431
|
G | T | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.222+12145G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519431 | ||||||
| chr3:134519434
|
G | A | 2 | a0002c0002t0001g0241a0002c0002t0001g0293 | 2 | NA18978.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.222+12148G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519434 | ||||||
| chr3:134519499
|
G | A | 191 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(188): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.222+12213G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519499 | ||||||
| chr3:134519564
|
A | T | 1 | a0001c0001t0004g0049 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.222+12278A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519564 | ||||||
| chr3:134519911
|
T | C | 211 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.223-11934T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519911 | ||||||
| chr3:134520017
|
G | A | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-11828G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520017 | ||||||
| chr3:134520062
|
T | G | 1 | a0001c0001t0002g0069 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.223-11783T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520062 | ||||||
| chr3:134520122
|
A | C | 191 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(188): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.223-11723A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520122 | ||||||
| chr3:134520186
|
C | T | 308 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(305): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.223-11659C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520186 | ||||||
| chr3:134520293
|
A | T | 1 | a0001c0001t0018g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.223-11552A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520293 | ||||||
| chr3:134520349
|
T | A | 191 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(188): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.223-11496T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520349 | ||||||
| chr3:134520559
|
C | G | 2 | a0001c0001t0002g0021a0001c0001t0002g0062 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.223-11286C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520559 | ||||||
| chr3:134520594
|
G | C | 1 | a0002c0002t0001g0276 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.223-11251G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520594 | ||||||
| chr3:134520675
|
A | T | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.223-11170A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520675 | ||||||
| chr3:134520702
|
G | T | 2 | a0001c0001t0014g0032a0001c0001t0014g0033 | 2 | HG01106.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.223-11143G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520702 | ||||||
| chr3:134520734
|
A | G | 7 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(4): Show | 7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-11111A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520734 | ||||||
| chr3:134520760
|
T | A | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.223-11085T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520760 | ||||||
| chr3:134520926
|
A | G | 5 | a0001c0003t0003g0154a0001c0003t0003g0155a0001c0003t0003g0168others(2): Show | 5 | HG00733.hp1 HG01123.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-10919A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520926 | ||||||
| chr3:134521446
|
TC | T | 308 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(305): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.223-10394delC | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134521446 | |||||
| chr3:134521451
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.223-10394C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134521451 | ||||||
| chr3:134521572
|
C | T | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.223-10273C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134521572 | ||||||
| chr3:134521707
|
C | T | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.223-10138C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134521707 | ||||||
| chr3:134521777
|
C | T | 7 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(4): Show | 7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-10068C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134521777 | ||||||
| chr3:134521792
|
A | C | 308 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(305): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.223-10053A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134521792 | ||||||
| chr3:134521928
|
G | C | 2 | a0002c0002t0001g0242a0002c0002t0001g0243 | 2 | HG03831.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.223-9917G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134521928 | ||||||
| chr3:134522397
|
TGAAA | T | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.223-9444_223-9441d others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134522397 | |||||
| chr3:134522468
|
A | T | 211 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.223-9377A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134522468 | ||||||
| chr3:134522535
|
G | A | 6 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(3): Show | 6 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.223-9310G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134522535 | ||||||
| chr3:134522726
|
T | A | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.223-9119T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134522726 | ||||||
| chr3:134522865
|
C | T | 1 | a0002c0002t0001g0237 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.223-8980C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134522865 | ||||||
| chr3:134522986
|
C | T | 2 | a0001c0001t0002g0021a0001c0001t0002g0062 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.223-8859C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134522986 | ||||||
| chr3:134523030
|
C | T | 1 | a0001c0003t0003g0158 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.223-8815C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523030 | ||||||
| chr3:134523060
|
T | C | 1 | a0001c0003t0003g0168 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.223-8785T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523060 | ||||||
| chr3:134523179
|
T | G | 90 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(87): Show | 95 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.223-8666T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523179 | ||||||
| chr3:134523209
|
T | A | 211 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.223-8636T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523209 | ||||||
| chr3:134523292
|
G | A | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.223-8553G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523292 | ||||||
| chr3:134523314
|
C | T | 5 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(2): Show | 5 | HG01109.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-8531C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523314 | ||||||
| chr3:134523341
|
C | A | 2 | a0001c0003t0003g0185a0001c0003t0023g0173 | 2 | HG02071.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.223-8504C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523341 | ||||||
| chr3:134523460
|
G | T | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.223-8385G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523460 | ||||||
| chr3:134523543
|
A | G | 2 | a0001c0001t0002g0029a0001c0001t0018g0030 | 2 | NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.223-8302A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523543 | ||||||
| chr3:134523594
|
A | G | 1 | a0001c0001t0002g0069 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.223-8251A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523594 | ||||||
| chr3:134523677
|
T | C | 1 | a0002c0002t0001g0308 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.223-8168T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523677 | ||||||
| chr3:134523756
|
T | C | 4 | a0001c0001t0009g0097a0001c0001t0009g0098a0001c0001t0009g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-8089T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523756 | ||||||
| chr3:134523821
|
G | A | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.223-8024G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523821 | ||||||
| chr3:134523982
|
G | A | 3 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111 | 3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.223-7863G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523982 | ||||||
| chr3:134523996
|
A | G | 2 | a0001c0001t0007g0115a0001c0001t0007g0116 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.223-7849A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523996 | ||||||
| chr3:134524033
|
T | C | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.223-7812T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134524033 | ||||||
| chr3:134524116
|
A | G | 3 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107 | 3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.223-7729A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134524116 | ||||||
| chr3:134524247
|
C | G | 9 | a0002c0002t0001g0226a0002c0002t0001g0237a0002c0002t0001g0240others(6): Show | 9 | HG01081.hp2 HG01346.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-7598C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134524247 | ||||||
| chr3:134524505
|
T | C | 11 | a0001c0001t0002g0074a0001c0001t0002g0083a0001c0001t0002g0084others(8): Show | 12 | HG00140.hp2 HG01099.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.223-7340T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134524505 | ||||||
| chr3:134524522
|
A | G | 1 | a0001c0003t0003g0194 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.223-7323A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134524522 | ||||||
| chr3:134524623
|
C | T | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.223-7222C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134524623 | ||||||
| chr3:134524702
|
G | A | 1 | a0001c0003t0003g0184 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.223-7143G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134524702 | ||||||
| chr3:134524965
|
C | T | 4 | a0001c0001t0002g0004a0001c0001t0002g0056a0001c0001t0002g0057others(1): Show | 5 | NA18972.hp1 NA18981.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-6880C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134524965 | ||||||
| chr3:134525009
|
C | T | 1 | a0001c0001t0021g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.223-6836C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525009 | ||||||
| chr3:134525072
|
C | T | 7 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(4): Show | 7 | HG02630.hp1 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-6773C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525072 | ||||||
| chr3:134525127
|
C | T | 1 | a0008c0008t0003g0182 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.223-6718C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525127 | ||||||
| chr3:134525193
|
C | T | 4 | a0002c0002t0001g0218a0002c0002t0001g0259a0002c0002t0001g0275others(1): Show | 4 | HG00609.hp1 NA18940.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-6652C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525193 | ||||||
| chr3:134525313
|
G | A | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.223-6532G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525313 | ||||||
| chr3:134525410
|
A | G | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.223-6435A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525410 | ||||||
| chr3:134525548
|
T | G | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.223-6297T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525548 | ||||||
| chr3:134525717
|
G | A | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.223-6128G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525717 | ||||||
| chr3:134525858
|
C | T | 4 | a0001c0001t0009g0097a0001c0001t0009g0098a0001c0001t0009g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-5987C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525858 | ||||||
| chr3:134525882
|
C | T | 1 | a0002c0002t0001g0236 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.223-5963C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525882 | ||||||
| chr3:134526117
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.223-5728G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526117 | ||||||
| chr3:134526149
|
C | T | 3 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107 | 3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.223-5696C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526149 | ||||||
| chr3:134526259
|
G | A | 308 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(305): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.223-5586G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526259 | ||||||
| chr3:134526272
|
G | C | 1 | a0005c0013t0007g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.223-5573G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526272 | ||||||
| chr3:134526318
|
T | A | 82 | a0001c0001t0001g0008a0002c0002t0001g0002a0002c0002t0001g0103others(79): Show | 85 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.223-5527T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526318 | ||||||
| chr3:134526434
|
C | T | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.223-5411C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526434 | ||||||
| chr3:134526459
|
C | T | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.223-5386C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526459 | ||||||
| chr3:134526486
|
C | G | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG01496.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.223-5359C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526486 | ||||||
| chr3:134526536
|
G | A | 1 | a0001c0003t0003g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.223-5309G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526536 | ||||||
| chr3:134526592
|
T | C | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.223-5253T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526592 | ||||||
| chr3:134526609
|
C | G | 5 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(2): Show | 5 | NA18941.hp2 NA18955.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-5236C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526609 | ||||||
| chr3:134526663
|
G | A | 12 | a0001c0001t0001g0211a0001c0001t0001g0221a0001c0001t0001g0263others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.223-5182G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526663 | ||||||
| chr3:134526870
|
G | A | 1 | a0001c0001t0002g0312 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.223-4975G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526870 | ||||||
| chr3:134526917
|
TG | T | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.223-4921delG | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134526917 | |||||
| chr3:134526921
|
G | C | 1 | a0001c0001t0002g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.223-4924G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526921 | ||||||
| chr3:134526954
|
G | T | 6 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(3): Show | 6 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.223-4891G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526954 | ||||||
| chr3:134527024
|
A | G | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.223-4821A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134527024 | ||||||
| chr3:134527087
|
T | C | 11 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(8): Show | 11 | HG01109.hp2 HG01123.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.223-4758T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134527087 | ||||||
| chr3:134527217
|
G | T | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.223-4628G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134527217 | ||||||
| chr3:134527252
|
A | T | 1 | a0002c0002t0001g0243 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.223-4593A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134527252 | ||||||
| chr3:134527870
|
A | AGTTCGGG others(15): Show |
2 | a0001c0003t0003g0165a0008c0008t0003g0182 | 2 | HG02015.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.223-3974_223-3953d others(24): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134527870 | |||||
| chr3:134527966
|
T | A | 308 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(305): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.223-3879T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134527966 | ||||||
| chr3:134527967
|
C | A | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.223-3878C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134527967 | ||||||
| chr3:134528361
|
C | G | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.223-3484C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134528361 | ||||||
| chr3:134528389
|
T | C | 191 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(188): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.223-3456T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134528389 | ||||||
| chr3:134528565
|
T | TGC | 19 | a0001c0001t0002g0017a0001c0001t0002g0059a0001c0001t0002g0064others(16): Show | 19 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.223-3279_223-3278i others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528565 | |||||
| chr3:134528567
|
T | C | 69 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(66): Show | 74 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.223-3278T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134528567 | ||||||
| chr3:134528569
|
C | CGT | 9 | a0001c0001t0006g0005a0001c0001t0006g0072a0001c0001t0006g0073others(6): Show | 10 | HG01175.hp1 HG01261.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.223-3252_223-3251d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | |||||
| chr3:134528569
|
C | CGTGT | 5 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091others(2): Show | 5 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-3254_223-3251d others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | |||||
| chr3:134528569
|
C | CGTGTGT | 68 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(65): Show | 70 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.223-3256_223-3251d others(8): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | |||||
| chr3:134528569
|
C | CGTGTGTA others(7): Show |
1 | a0001c0001t0009g0099 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.223-3270_223-3269i others(16): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | |||||
| chr3:134528569
|
C | CGTGTGTG others(1): Show |
20 | a0001c0001t0001g0149a0001c0001t0001g0206a0001c0001t0001g0207others(17): Show | 20 | HG00140.hp1 HG01109.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.223-3258_223-3251d others(10): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | |||||
| chr3:134528569
|
C | CGTGTGTG others(3): Show |
89 | a0001c0001t0001g0008a0001c0001t0001g0216a0001c0001t0001g0286others(86): Show | 92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.223-3260_223-3251d others(12): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | |||||
| chr3:134528569
|
C | CGTGTGTG others(5): Show |
13 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265others(10): Show | 13 | HG01081.hp2 HG01496.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.223-3262_223-3251d others(14): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | |||||
| chr3:134528569
|
C | CGTGTGTG others(7): Show |
7 | a0001c0001t0001g0211a0001c0001t0005g0122a0001c0001t0009g0097others(4): Show | 7 | HG01109.hp1 HG01243.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-3264_223-3251d others(16): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | |||||
| chr3:134528569
|
C | CGTGTGTG others(9): Show |
6 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0123others(3): Show | 6 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.223-3266_223-3251d others(18): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | |||||
| chr3:134528569
|
C | CGTGTGTG others(11): Show |
4 | a0001c0001t0005g0124a0001c0001t0005g0127a0001c0001t0025g0119others(1): Show | 4 | HG02818.hp1 HG03540.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-3268_223-3251d others(20): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | |||||
| chr3:134528569
|
C | T | 84 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(81): Show | 88 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.223-3276C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134528569 | ||||||
| chr3:134528594
|
G | GTGTGTGT others(4): Show |
1 | a0002c0002t0001g0262 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.223-3251_223-3250i others(13): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134528594 | ||||||
| chr3:134528759
|
G | A | 23 | a0001c0001t0004g0001a0001c0001t0004g0019a0001c0001t0004g0020others(20): Show | 25 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.223-3086G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134528759 | ||||||
| chr3:134528864
|
A | C | 26 | a0001c0001t0002g0017a0001c0001t0002g0064a0001c0001t0002g0065others(23): Show | 27 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.223-2981A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134528864 | ||||||
| chr3:134529021
|
C | A | 304 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(301): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.223-2824C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134529021 | ||||||
| chr3:134529026
|
A | G | 3 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111 | 3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.223-2819A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134529026 | ||||||
| chr3:134529168
|
G | C | 304 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(301): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.223-2677G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134529168 | ||||||
| chr3:134529185
|
G | A | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-2660G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134529185 | ||||||
| chr3:134529339
|
C | CT | 96 | a0001c0001t0001g0305a0001c0001t0002g0003a0001c0001t0002g0004others(93): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.223-2487dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134529339 | |||||
| chr3:134529339
|
C | CTT | 189 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(186): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.223-2488_223-2487d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134529339 | |||||
| chr3:134529339
|
C | CTTT | 7 | a0001c0001t0001g0139a0001c0001t0001g0300a0001c0001t0021g0108others(4): Show | 7 | HG01099.hp2 HG02071.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-2489_223-2487d others(5): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134529339 | |||||
| chr3:134529444
|
G | A | 7 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(4): Show | 7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-2401G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134529444 | ||||||
| chr3:134529576
|
A | G | 2 | a0001c0001t0015g0144a0001c0001t0015g0145 | 2 | HG01169.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.223-2269A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134529576 | ||||||
| chr3:134529604
|
G | A | 1 | a0001c0001t0004g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.223-2241G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134529604 | ||||||
| chr3:134529672
|
C | A | 1 | a0002c0002t0001g0223 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.223-2173C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134529672 | ||||||
| chr3:134529868
|
A | AT | 229 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(226): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.223-1953dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134529868 | |||||
| chr3:134529868
|
A | ATT | 44 | a0001c0001t0001g0008a0001c0001t0001g0206a0001c0001t0001g0207others(41): Show | 45 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.223-1954_223-1953d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134529868 | |||||
| chr3:134529868
|
A | ATTT | 11 | a0001c0001t0001g0208a0001c0001t0001g0300a0001c0001t0002g0028others(8): Show | 11 | HG01891.hp1 HG03540.hp2 HG04115.hp2 others(8): Show |
intron_variant | MODIFIER | c.223-1955_223-1953d others(5): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134529868 | |||||
| chr3:134529959
|
C | T | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.223-1886C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134529959 | ||||||
| chr3:134530027
|
C | T | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.223-1818C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530027 | ||||||
| chr3:134530064
|
G | T | 6 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(3): Show | 6 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.223-1781G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530064 | ||||||
| chr3:134530118
|
C | T | 1 | a0001c0001t0004g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.223-1727C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530118 | ||||||
| chr3:134530162
|
C | T | 1 | a0001c0003t0001g0134 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.223-1683C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530162 | ||||||
| chr3:134530209
|
C | T | 1 | a0001c0001t0005g0126 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.223-1636C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530209 | ||||||
| chr3:134530505
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.223-1340T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530505 | ||||||
| chr3:134530574
|
T | C | 1 | a0001c0001t0002g0084 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.223-1271T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530574 | ||||||
| chr3:134530829
|
T | C | 1 | a0002c0002t0001g0285 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.223-1016T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530829 | ||||||
| chr3:134530927
|
C | G | 195 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(192): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.223-918C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530927 | ||||||
| chr3:134530946
|
C | T | 5 | a0002c0002t0001g0218a0002c0002t0001g0259a0002c0002t0001g0275others(2): Show | 5 | HG00609.hp1 NA18940.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-899C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530946 | ||||||
| chr3:134530970
|
G | A | 1 | a0007c0009t0001g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.223-875G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530970 | ||||||
| chr3:134531057
|
A | G | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.223-788A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134531057 | ||||||
| chr3:134531072
|
C | T | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-773C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134531072 | ||||||
| chr3:134531129
|
G | A | 5 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0001t0002g0068others(2): Show | 5 | NA18939.hp2 NA18999.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-716G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134531129 | ||||||
| chr3:134531257
|
G | T | 90 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(87): Show | 95 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.223-588G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134531257 | ||||||
| chr3:134531294
|
C | G | 3 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307 | 3 | HG00280.hp2 HG00733.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.223-551C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134531294 | ||||||
| chr3:134531483
|
C | T | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.223-362C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134531483 | ||||||
| chr3:134531553
|
G | A | 3 | a0001c0001t0001g0216a0001c0001t0001g0289a0001c0010t0001g0290 | 3 | HG00323.hp2 HG02300.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.223-292G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134531553 | ||||||
| chr3:134531734
|
T | C | 1 | a0001c0001t0021g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.223-111T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134531734 | ||||||
| chr3:134531766
|
G | T | 1 | a0001c0003t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.223-79G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134531766 | ||||||
| chr3:134531969
|
G | A | 8 | a0001c0001t0005g0120a0001c0001t0005g0122a0001c0001t0005g0123others(5): Show | 8 | NA18940.hp2 NA18951.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.318+29G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 4/14 | chr3 | 134531969 | ||||||
| chr3:134532053
|
A | G | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.318+113A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 4/14 | chr3 | 134532053 | ||||||
| chr3:134532197
|
A | G | 309 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(306): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.318+257A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 4/14 | chr3 | 134532197 | ||||||
| chr3:134532326
|
A | C | 1 | a0001c0001t0001g0287 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.318+386A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 4/14 | chr3 | 134532326 | ||||||
| chr3:134532342
|
A | G | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.318+402A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 4/14 | chr3 | 134532342 | ||||||
| chr3:134532540
|
T | G | 13 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(10): Show | 13 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.319-238T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 4/14 | chr3 | 134532540 | ||||||
| chr3:134532564
|
A | T | 1 | a0002c0002t0001g0285 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.319-214A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 4/14 | chr3 | 134532564 | ||||||
| chr3:134532573
|
A | T | 1 | a0001c0001t0001g0221 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.319-205A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 4/14 | chr3 | 134532573 | ||||||
| chr3:134532634
|
T | C | 1 | a0001c0001t0011g0110 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.319-144T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 4/14 | chr3 | 134532634 | ||||||
| chr3:134533017
|
A | G | 1 | a0001c0003t0003g0179 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.441+117A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533017 | ||||||
| chr3:134533052
|
C | T | 6 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(3): Show | 6 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+152C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533052 | ||||||
| chr3:134533272
|
C | T | 191 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(188): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.441+372C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533272 | ||||||
| chr3:134533292
|
A | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.441+392A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533292 | ||||||
| chr3:134533372
|
C | T | 1 | a0002c0002t0001g0242 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.441+472C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533372 | ||||||
| chr3:134533508
|
A | G | 1 | a0001c0001t0024g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.441+608A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533508 | ||||||
| chr3:134533543
|
T | C | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.441+643T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533543 | ||||||
| chr3:134533611
|
C | G | 1 | a0001c0001t0004g0019 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.441+711C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533611 | ||||||
| chr3:134533620
|
C | T | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.441+720C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533620 | ||||||
| chr3:134533649
|
G | T | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.441+749G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533649 | ||||||
| chr3:134534412
|
A | G | 2 | a0002c0002t0001g0254a0002c0002t0001g0274 | 2 | HG00423.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.441+1512A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134534412 | ||||||
| chr3:134534755
|
T | C | 13 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(10): Show | 13 | HG02572.hp1 HG03139.hp1 HG03579.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+1855T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134534755 | ||||||
| chr3:134534803
|
A | G | 14 | a0001c0001t0001g0008a0001c0001t0001g0216a0001c0001t0001g0286others(11): Show | 15 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+1903A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134534803 | ||||||
| chr3:134534889
|
T | C | 2 | a0002c0002t0001g0238a0002c0002t0001g0245 | 2 | HG01884.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.441+1989T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134534889 | ||||||
| chr3:134535079
|
A | G | 4 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(1): Show | 4 | HG02572.hp1 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-2076A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134535079 | ||||||
| chr3:134535209
|
G | A | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-1946G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134535209 | ||||||
| chr3:134535340
|
C | T | 1 | a0001c0001t0002g0066 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.442-1815C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134535340 | ||||||
| chr3:134535495
|
C | CT | 186 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(183): Show | 191 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.442-1657dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 134535495 | |||||
| chr3:134535495
|
C | CTT | 5 | a0001c0003t0001g0153a0001c0003t0003g0170a0001c0003t0003g0171others(2): Show | 5 | HG00280.hp1 HG01106.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-1658_442-1657d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 134535495 | |||||
| chr3:134535498
|
TC | T | 91 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(88): Show | 96 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.442-1655delC | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 134535498 | |||||
| chr3:134535499
|
C | T | 217 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(214): Show | 222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.442-1656C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134535499 | ||||||
| chr3:134535500
|
C | T | 308 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(305): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.442-1655C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134535500 | ||||||
| chr3:134535665
|
A | T | 1 | a0001c0003t0003g0161 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.442-1490A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134535665 | ||||||
| chr3:134535788
|
G | A | 1 | a0001c0001t0013g0088 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.442-1367G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134535788 | ||||||
| chr3:134535870
|
A | G | 6 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0001t0002g0068others(3): Show | 6 | NA18939.hp2 NA18999.hp2 NA19066.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-1285A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134535870 | ||||||
| chr3:134536062
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.442-1093C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536062 | ||||||
| chr3:134536147
|
C | G | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.442-1008C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536147 | ||||||
| chr3:134536149
|
A | G | 198 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(195): Show | 203 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.442-1006A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536149 | ||||||
| chr3:134536153
|
C | G | 90 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(87): Show | 95 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.442-1002C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536153 | ||||||
| chr3:134536189
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.442-966C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536189 | ||||||
| chr3:134536300
|
A | T | 1 | a0002c0002t0001g0278 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.442-855A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536300 | ||||||
| chr3:134536410
|
G | C | 3 | a0001c0001t0007g0114a0001c0001t0007g0115a0001c0001t0007g0116 | 3 | HG02572.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.442-745G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536410 | ||||||
| chr3:134536457
|
C | T | 4 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-698C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536457 | ||||||
| chr3:134536834
|
A | T | 1 | a0001c0003t0003g0157 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.442-321A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536834 | ||||||
| chr3:134536909
|
T | G | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-246T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536909 | ||||||
| chr3:134536912
|
G | T | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-243G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536912 | ||||||
| chr3:134537091
|
G | A | 1 | a0001c0001t0002g0018 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.442-64G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134537091 | ||||||
| chr3:134537317
|
A | G | 97 | a0001c0001t0001g0008a0001c0001t0001g0216a0001c0001t0001g0286others(94): Show | 100 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.555+49A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134537317 | ||||||
| chr3:134537378
|
C | T | 8 | a0002c0002t0001g0236a0002c0002t0001g0239a0002c0002t0001g0242others(5): Show | 8 | HG01981.hp1 HG02698.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.555+110C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134537378 | ||||||
| chr3:134537404
|
C | T | 1 | a0001c0001t0005g0126 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.555+136C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134537404 | ||||||
| chr3:134537628
|
C | T | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.555+360C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134537628 | ||||||
| chr3:134537658
|
C | T | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.555+390C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134537658 | ||||||
| chr3:134537789
|
G | A | 1 | a0001c0003t0003g0174 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.555+521G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134537789 | ||||||
| chr3:134538058
|
G | A | 3 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096 | 3 | HG00099.hp1 HG02683.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.555+790G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134538058 | ||||||
| chr3:134538198
|
G | GT | 7 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0054others(4): Show | 7 | HG00140.hp2 HG01175.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.555+950dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538198 | |||||
| chr3:134538198
|
G | GTTT | 8 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(5): Show | 8 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.555+948_555+950dup others(3): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538198 | |||||
| chr3:134538198
|
GT | G | 30 | a0001c0001t0001g0221a0001c0001t0001g0266a0001c0001t0001g0286others(27): Show | 30 | HG00099.hp1 HG00733.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.555+950delT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538198 | |||||
| chr3:134538198
|
GTT | G | 161 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(158): Show | 165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.555+949_555+950del others(2): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538198 | |||||
| chr3:134538198
|
GTTT | G | 10 | a0001c0001t0001g0131a0001c0003t0001g0006a0001c0003t0001g0140others(7): Show | 11 | HG00741.hp1 HG02895.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.555+948_555+950del others(3): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538198 | |||||
| chr3:134538328
|
C | T | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.555+1060C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134538328 | ||||||
| chr3:134538372
|
G | T | 4 | a0001c0001t0009g0097a0001c0001t0009g0098a0001c0001t0009g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+1104G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134538372 | ||||||
| chr3:134538397
|
A | G | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.555+1129A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134538397 | ||||||
| chr3:134538474
|
G | GT | 8 | a0001c0003t0003g0191a0001c0003t0003g0196a0001c0003t0003g0200others(5): Show | 8 | HG00423.hp1 HG02523.hp1 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.555+1213dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538474 | |||||
| chr3:134538517
|
G | T | 2 | a0001c0001t0009g0097a0001c0001t0009g0098 | 2 | HG01243.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.555+1249G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134538517 | ||||||
| chr3:134538529
|
G | GTGTATAT others(23): Show |
1 | a0002c0002t0001g0291 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.555+1264_555+1265i others(32): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538529 | |||||
| chr3:134538529
|
G | GTGTATAT others(25): Show |
1 | a0002c0002t0001g0292 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.555+1264_555+1265i others(34): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538529 | |||||
| chr3:134538529
|
G | GTGTATAT others(27): Show |
1 | a0002c0002t0001g0236 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.555+1264_555+1265i others(36): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538529 | |||||
| chr3:134538531
|
G | GTA | 67 | a0001c0001t0002g0009a0001c0001t0002g0015a0001c0001t0002g0016others(64): Show | 70 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.555+1264_555+1265i others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATA | 91 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(88): Show | 93 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.555+1264_555+1265i others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATATA | 42 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0149others(39): Show | 45 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.555+1264_555+1265i others(8): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATATAT others(1): Show |
7 | a0001c0001t0001g0299a0001c0001t0002g0060a0001c0001t0002g0104others(4): Show | 7 | HG00609.hp2 HG01255.hp2 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.555+1264_555+1265i others(10): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATATAT others(3): Show |
2 | a0001c0001t0009g0097a0001c0003t0003g0204 | 2 | HG01069.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.555+1264_555+1265i others(12): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATATAT others(15): Show |
1 | a0002c0002t0001g0223 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.555+1264_555+1265i others(24): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATATAT others(33): Show |
2 | a0002c0002t0001g0238a0002c0002t0001g0243 | 2 | HG01884.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.555+1264_555+1265i others(42): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATATAT others(35): Show |
3 | a0002c0002t0001g0239a0002c0002t0001g0245a0002c0002t0001g0252 | 3 | HG01981.hp1 NA18969.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.555+1264_555+1265i others(44): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATATAT others(31): Show |
2 | a0002c0002t0001g0242a0002c0002t0001g0280 | 2 | HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.555+1264_555+1265i others(40): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATATAT others(29): Show |
9 | a0002c0002t0001g0214a0002c0002t0001g0241a0002c0002t0001g0253others(6): Show | 9 | HG00735.hp1 HG01099.hp2 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.555+1264_555+1265i others(38): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATATAT others(31): Show |
1 | a0002c0002t0001g0258 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.555+1264_555+1265i others(40): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATATAT others(25): Show |
1 | a0002c0002t0001g0282 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.555+1264_555+1265i others(34): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATATAT others(27): Show |
1 | a0002c0002t0001g0256 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.555+1264_555+1265i others(36): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATATAT others(55): Show |
2 | a0002c0002t0001g0212a0002c0002t0001g0267 | 2 | NA18965.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.555+1264_555+1265i others(64): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATATAT others(23): Show |
2 | a0002c0002t0001g0233a0002c0002t0001g0234 | 2 | NA18950.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.555+1264_555+1265i others(32): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATATAT others(25): Show |
31 | a0002c0002t0001g0002a0002c0002t0001g0209a0002c0002t0001g0215others(28): Show | 33 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.555+1264_555+1265i others(34): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATATAT others(27): Show |
13 | a0002c0002t0001g0224a0002c0002t0001g0225a0002c0002t0001g0244others(10): Show | 13 | HG00544.hp1 HG00609.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.555+1264_555+1265i others(36): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATATAT others(29): Show |
3 | a0002c0002t0001g0268a0002c0002t0001g0298a0002c0002t0022g0246 | 3 | HG01258.hp1 HG02015.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.555+1264_555+1265i others(38): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATATAT others(33): Show |
1 | a0002c0002t0001g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.555+1264_555+1265i others(42): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATATAT others(55): Show |
1 | a0002c0002t0001g0303 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.555+1264_555+1265i others(64): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538531
|
G | GTATATAT others(27): Show |
1 | a0002c0002t0001g0251 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.555+1264_555+1265i others(36): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | |||||
| chr3:134538533
|
G | A | 290 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(287): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.555+1265G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134538533 | ||||||
| chr3:134538533
|
G | GTA | 4 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+1285_555+1286d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538533 | |||||
| chr3:134538533
|
G | GTATA | 9 | a0001c0001t0001g0211a0001c0001t0001g0221a0001c0001t0001g0263others(6): Show | 9 | HG01496.hp2 HG02280.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.555+1283_555+1286d others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538533 | |||||
| chr3:134538567
|
T | A | 1 | a0001c0001t0005g0122 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.555+1299T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134538567 | ||||||
| chr3:134538698
|
G | A | 1 | a0001c0001t0004g0049 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.555+1430G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134538698 | ||||||
| chr3:134539275
|
A | ATT | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.555+2011_555+2012d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134539275 | |||||
| chr3:134539452
|
T | A | 3 | a0001c0001t0006g0005a0001c0001t0006g0072a0001c0001t0006g0080 | 4 | HG01346.hp1 HG01981.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.555+2184T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134539452 | ||||||
| chr3:134539692
|
T | TA | 7 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(4): Show | 7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.555+2433dupA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134539692 | |||||
| chr3:134539863
|
A | C | 2 | a0001c0003t0001g0134a0001c0003t0001g0140 | 2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.555+2595A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134539863 | ||||||
| chr3:134540004
|
C | T | 4 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(1): Show | 4 | HG02572.hp1 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+2736C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134540004 | ||||||
| chr3:134540284
|
T | G | 308 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(305): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.555+3016T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134540284 | ||||||
| chr3:134540361
|
C | T | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.555+3093C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134540361 | ||||||
| chr3:134540604
|
T | A | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.555+3336T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134540604 | ||||||
| chr3:134540764
|
A | AT | 243 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(240): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.555+3514dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134540764 | |||||
| chr3:134540764
|
A | ATT | 7 | a0001c0001t0001g0286a0001c0001t0005g0121a0001c0001t0024g0117others(4): Show | 7 | HG02056.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.555+3513_555+3514d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134540764 | |||||
| chr3:134540783
|
A | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.555+3515A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134540783 | ||||||
| chr3:134540811
|
T | C | 20 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(17): Show | 20 | HG01109.hp2 HG01123.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.555+3543T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134540811 | ||||||
| chr3:134540938
|
C | T | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.555+3670C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134540938 | ||||||
| chr3:134540969
|
A | T | 1 | a0001c0001t0024g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.555+3701A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134540969 | ||||||
| chr3:134541061
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.555+3793C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541061 | ||||||
| chr3:134541112
|
C | T | 90 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(87): Show | 95 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.555+3844C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541112 | ||||||
| chr3:134541145
|
T | C | 1 | a0001c0003t0003g0157 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.555+3877T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541145 | ||||||
| chr3:134541199
|
C | G | 6 | a0001c0003t0003g0191a0001c0003t0003g0196a0001c0003t0003g0200others(3): Show | 6 | HG00423.hp1 HG02523.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.555+3931C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541199 | ||||||
| chr3:134541510
|
C | CT | 24 | a0001c0001t0001g0265a0001c0001t0001g0286a0001c0001t0001g0305others(21): Show | 24 | HG00280.hp2 HG00738.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.556-4054dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134541510 | |||||
| chr3:134541510
|
CT | C | 7 | a0001c0001t0001g0139a0001c0001t0002g0076a0001c0001t0002g0077others(4): Show | 7 | HG01069.hp2 HG01516.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-4054delT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134541510 | |||||
| chr3:134541602
|
G | A | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.556-3984G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541602 | ||||||
| chr3:134541655
|
A | C | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.556-3931A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541655 | ||||||
| chr3:134541658
|
C | T | 1 | a0002c0002t0001g0311 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.556-3928C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541658 | ||||||
| chr3:134541733
|
G | A | 1 | a0002c0002t0001g0268 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.556-3853G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541733 | ||||||
| chr3:134541753
|
TC | T | 90 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(87): Show | 95 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.556-3831delC | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134541753 | |||||
| chr3:134541759
|
C | T | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.556-3827C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541759 | ||||||
| chr3:134541843
|
G | T | 1 | a0001c0001t0004g0295 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.556-3743G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541843 | ||||||
| chr3:134541873
|
A | G | 1 | a0001c0001t0004g0295 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.556-3713A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541873 | ||||||
| chr3:134541921
|
A | C | 308 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(305): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.556-3665A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541921 | ||||||
| chr3:134541972
|
A | C | 53 | a0001c0003t0003g0154a0001c0003t0003g0155a0001c0003t0003g0156others(50): Show | 54 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.556-3614A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541972 | ||||||
| chr3:134542018
|
G | A | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.556-3568G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542018 | ||||||
| chr3:134542023
|
G | A | 3 | a0001c0001t0002g0016a0001c0001t0002g0031a0001c0001t0002g0041 | 3 | HG01243.hp2 HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.556-3563G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542023 | ||||||
| chr3:134542273
|
T | A | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.556-3313T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542273 | ||||||
| chr3:134542281
|
C | T | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.556-3305C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542281 | ||||||
| chr3:134542402
|
C | A | 1 | a0001c0003t0003g0157 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.556-3184C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542402 | ||||||
| chr3:134542403
|
A | C | 1 | a0001c0003t0003g0157 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.556-3183A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542403 | ||||||
| chr3:134542500
|
G | T | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.556-3086G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542500 | ||||||
| chr3:134542595
|
T | C | 211 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.556-2991T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542595 | ||||||
| chr3:134542596
|
T | C | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.556-2990T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542596 | ||||||
| chr3:134542705
|
C | A | 1 | a0001c0001t0024g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.556-2881C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542705 | ||||||
| chr3:134542812
|
C | T | 211 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.556-2774C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542812 | ||||||
| chr3:134542940
|
C | CA | 99 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(96): Show | 104 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.556-2633dupA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134542940 | |||||
| chr3:134542940
|
C | CAA | 193 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(190): Show | 198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.556-2634_556-2633d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134542940 | |||||
| chr3:134542940
|
C | CAAA | 13 | a0001c0001t0001g0142a0001c0001t0005g0120a0001c0001t0005g0121others(10): Show | 13 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.556-2635_556-2633d others(5): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134542940 | |||||
| chr3:134543248
|
A | G | 7 | a0001c0001t0004g0042a0001c0003t0003g0166a0001c0003t0003g0167others(4): Show | 7 | HG02056.hp1 HG02155.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.556-2338A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134543248 | ||||||
| chr3:134543406
|
T | A | 1 | a0001c0003t0003g0157 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.556-2180T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134543406 | ||||||
| chr3:134543779
|
C | T | 1 | a0002c0002t0001g0239 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.556-1807C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134543779 | ||||||
| chr3:134543845
|
AG | A | 191 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(188): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.556-1740delG | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134543845 | ||||||
| chr3:134543846
|
G | A | 117 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(114): Show | 122 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.556-1740G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134543846 | ||||||
| chr3:134543961
|
T | TA | 7 | a0001c0001t0002g0015a0001c0001t0002g0025a0001c0001t0010g0086others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.556-1612dupA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134543961 | |||||
| chr3:134543961
|
TA | T | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.556-1612delA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134543961 | |||||
| chr3:134544055
|
C | G | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.556-1531C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544055 | ||||||
| chr3:134544151
|
G | A | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.556-1435G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544151 | ||||||
| chr3:134544248
|
C | T | 4 | a0001c0001t0002g0004a0001c0001t0002g0056a0001c0001t0002g0057others(1): Show | 5 | NA18972.hp1 NA18981.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.556-1338C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544248 | ||||||
| chr3:134544309
|
T | C | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.556-1277T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544309 | ||||||
| chr3:134544333
|
T | C | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.556-1253T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544333 | ||||||
| chr3:134544414
|
T | A | 1 | a0001c0003t0003g0179 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.556-1172T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544414 | ||||||
| chr3:134544511
|
C | T | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.556-1075C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544511 | ||||||
| chr3:134544631
|
C | G | 1 | a0002c0002t0001g0253 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.556-955C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544631 | ||||||
| chr3:134544636
|
T | G | 2 | a0001c0001t0011g0109a0001c0001t0011g0111 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.556-950T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544636 | ||||||
| chr3:134544636
|
T | TGG | 178 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(175): Show | 182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.556-942_556-941dup others(2): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134544636 | |||||
| chr3:134544696
|
A | G | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.556-890A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544696 | ||||||
| chr3:134544770
|
G | A | 1 | a0002c0002t0001g0228 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.556-816G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544770 | ||||||
| chr3:134544895
|
C | T | 1 | a0001c0001t0024g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.556-691C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544895 | ||||||
| chr3:134544957
|
C | T | 1 | a0001c0001t0006g0082 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.556-629C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544957 | ||||||
| chr3:134545079
|
C | T | 4 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(1): Show | 4 | HG02572.hp1 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-507C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134545079 | ||||||
| chr3:134545080
|
A | G | 309 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(306): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.556-506A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134545080 | ||||||
| chr3:134545148
|
C | T | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.556-438C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134545148 | ||||||
| chr3:134545149
|
G | A | 191 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(188): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.556-437G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134545149 | ||||||
| chr3:134545200
|
T | C | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.556-386T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134545200 | ||||||
| chr3:134545218
|
C | T | 2 | a0001c0001t0002g0029a0001c0001t0018g0030 | 2 | NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.556-368C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134545218 | ||||||
| chr3:134545350
|
G | A | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.556-236G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134545350 | ||||||
| chr3:134545376
|
T | C | 309 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(306): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.556-210T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134545376 | ||||||
| chr3:134545450
|
T | C | 1 | a0001c0003t0027g0163 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.556-136T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134545450 | ||||||
| chr3:134545455
|
AAT | A | 295 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(292): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.556-116_556-115del others(2): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134545455 | |||||
| chr3:134545886
|
G | A | 1 | a0001c0003t0001g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.789+67G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/14 | chr3 | 134545886 | ||||||
| chr3:134545924
|
C | G | 3 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107 | 3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.789+105C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/14 | chr3 | 134545924 | ||||||
| chr3:134545966
|
T | C | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.789+147T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/14 | chr3 | 134545966 | ||||||
| chr3:134546008
|
G | A | 1 | a0002c0002t0001g0283 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.790-141G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/14 | chr3 | 134546008 | ||||||
| chr3:134546017
|
A | C | 191 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(188): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.790-132A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/14 | chr3 | 134546017 | ||||||
| chr3:134546038
|
G | C | 1 | a0007c0009t0001g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.790-111G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/14 | chr3 | 134546038 | ||||||
| chr3:134546079
|
C | A | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.790-70C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/14 | chr3 | 134546079 | ||||||
| chr3:134546081
|
G | A | 8 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(5): Show | 8 | HG00738.hp2 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.790-68G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/14 | chr3 | 134546081 | ||||||
| chr3:134546113
|
G | C | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.790-36G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/14 | chr3 | 134546113 | ||||||
| chr3:134546365
|
T | A | 4 | a0002c0002t0001g0226a0002c0002t0001g0237a0002c0002t0001g0240others(1): Show | 4 | HG01346.hp2 HG01993.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.929+77T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134546365 | ||||||
| chr3:134546450
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.929+162C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134546450 | ||||||
| chr3:134546451
|
G | C | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.929+163G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134546451 | ||||||
| chr3:134546678
|
A | G | 1 | a0001c0003t0003g0156 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.929+390A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134546678 | ||||||
| chr3:134546846
|
G | C | 1 | a0001c0001t0002g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.930-489G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134546846 | ||||||
| chr3:134546907
|
C | T | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.930-428C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134546907 | ||||||
| chr3:134547001
|
A | G | 308 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(305): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.930-334A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134547001 | ||||||
| chr3:134547109
|
A | G | 8 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(5): Show | 8 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.930-226A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134547109 | ||||||
| chr3:134547282
|
A | G | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.930-53A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134547282 | ||||||
| chr3:134547306
|
G | C | 308 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(305): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.930-29G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134547306 | ||||||
| chr3:134547479
|
A | G | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
splice_region_variant&intron_variant | LOW | c.1067+7A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134547479 | ||||||
| chr3:134547485
|
A | G | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1067+13A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134547485 | ||||||
| chr3:134547605
|
T | G | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1067+133T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134547605 | ||||||
| chr3:134547614
|
C | CTTTTTTT others(3): Show |
1 | a0002c0002t0001g0280 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1067+148_1067+157d others(12): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | |||||
| chr3:134547614
|
C | CTTTTTTT others(6): Show |
5 | a0001c0001t0007g0113a0001c0001t0007g0115a0001c0001t0007g0116others(2): Show | 5 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1067+145_1067+157d others(15): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | |||||
| chr3:134547614
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1067+144_1067+157d others(16): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | |||||
| chr3:134547614
|
C | CTTTTTTT others(8): Show |
3 | a0001c0003t0003g0170a0001c0003t0003g0171a0007c0009t0001g0135 | 3 | HG03491.hp2 HG03492.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1067+143_1067+157d others(17): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | |||||
| chr3:134547614
|
C | CTTTTTTT others(9): Show |
53 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(50): Show | 54 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1067+157_1067+158i others(18): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | |||||
| chr3:134547614
|
C | CTTTTTTT others(10): Show |
26 | a0001c0001t0001g0138a0001c0001t0001g0149a0001c0001t0001g0207others(23): Show | 27 | HG01496.hp2 HG01891.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.1067+157_1067+158i others(19): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | |||||
| chr3:134547614
|
C | CTTTTTTT others(11): Show |
11 | a0001c0001t0001g0148a0001c0001t0001g0302a0001c0001t0029g0136others(8): Show | 11 | HG00741.hp1 HG02145.hp2 HG03195.hp1 others(8): Show |
intron_variant | MODIFIER | c.1067+157_1067+158i others(20): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | |||||
| chr3:134547614
|
C | CTTTTTTT others(12): Show |
9 | a0001c0001t0001g0287a0001c0001t0001g0305a0001c0001t0001g0306others(6): Show | 9 | HG00140.hp1 HG00280.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1067+157_1067+158i others(21): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | |||||
| chr3:134547614
|
C | CTTTTTTT others(13): Show |
26 | a0001c0001t0001g0288a0001c0001t0001g0307a0001c0003t0003g0203others(23): Show | 28 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.1067+157_1067+158i others(22): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | |||||
| chr3:134547614
|
C | CTTTTTTT others(14): Show |
32 | a0001c0001t0001g0008a0001c0001t0001g0216a0001c0001t0001g0286others(29): Show | 33 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1067+157_1067+158i others(23): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | |||||
| chr3:134547614
|
C | CTTTTTTT others(15): Show |
22 | a0002c0002t0001g0212a0002c0002t0001g0213a0002c0002t0001g0231others(19): Show | 22 | HG00323.hp1 HG00738.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1067+157_1067+158i others(24): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | |||||
| chr3:134547614
|
C | CTTTTTTT others(16): Show |
5 | a0001c0001t0001g0300a0002c0002t0001g0223a0002c0002t0001g0238others(2): Show | 5 | HG01168.hp1 HG01884.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.1067+157_1067+158i others(25): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | |||||
| chr3:134547614
|
C | CTTTTTTT others(17): Show |
1 | a0002c0002t0001g0292 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1067+157_1067+158i others(26): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | |||||
| chr3:134547614
|
C | CTTTTTTT others(18): Show |
1 | a0002c0002t0001g0103 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1067+157_1067+158i others(27): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | |||||
| chr3:134547614
|
CTT | C | 8 | a0001c0001t0005g0121a0001c0001t0005g0122a0001c0001t0005g0123others(5): Show | 8 | HG03704.hp1 NA18940.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.1067+156_1067+157d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | |||||
| chr3:134547614
|
CTTT | C | 94 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(91): Show | 99 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.1067+155_1067+157d others(5): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | |||||
| chr3:134547634
|
C | T | 7 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(4): Show | 7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1067+162C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134547634 | ||||||
| chr3:134547636
|
G | C | 6 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(3): Show | 6 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1067+164G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134547636 | ||||||
| chr3:134547691
|
A | G | 1 | a0001c0001t0024g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1067+219A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134547691 | ||||||
| chr3:134547916
|
C | G | 1 | a0001c0001t0004g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1067+444C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134547916 | ||||||
| chr3:134548144
|
G | A | 1 | a0002c0002t0022g0246 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1067+672G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134548144 | ||||||
| chr3:134548259
|
T | G | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.1067+787T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134548259 | ||||||
| chr3:134548523
|
T | A | 1 | a0002c0002t0001g0256 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1068-539T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134548523 | ||||||
| chr3:134548650
|
AGTAATAC others(7): Show |
A | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1068-409_1068-396d others(16): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134548650 | |||||
| chr3:134548677
|
A | G | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1068-385A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134548677 | ||||||
| chr3:134548810
|
A | G | 1 | a0001c0001t0002g0023 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1068-252A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134548810 | ||||||
| chr3:134548836
|
C | T | 1 | a0001c0001t0006g0072 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1068-226C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134548836 | ||||||
| chr3:134548935
|
A | G | 1 | a0002c0002t0001g0291 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1068-127A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134548935 | ||||||
| chr3:134549207
|
T | C | 1 | a0007c0009t0001g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1182+31T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549207 | ||||||
| chr3:134549211
|
A | G | 7 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(4): Show | 7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1182+35A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549211 | ||||||
| chr3:134549329
|
T | A | 3 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107 | 3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1182+153T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549329 | ||||||
| chr3:134549357
|
C | T | 1 | a0001c0001t0002g0312 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1182+181C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549357 | ||||||
| chr3:134549429
|
A | T | 1 | a0002c0002t0001g0256 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1182+253A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549429 | ||||||
| chr3:134549777
|
A | G | 191 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(188): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1183-286A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549777 | ||||||
| chr3:134549782
|
T | C | 2 | a0002c0002t0001g0224a0002c0002t0001g0225 | 2 | HG00544.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1183-281T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549782 | ||||||
| chr3:134549857
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1183-206G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549857 | ||||||
| chr3:134549895
|
A | C | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1183-168A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549895 | ||||||
| chr3:134549905
|
T | C | 1 | a0001c0001t0002g0078 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1183-158T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549905 | ||||||
| chr3:134550059
|
A | G | 2 | a0002c0002t0001g0260a0002c0002t0001g0262 | 2 | NA19006.hp2 NA19066.hp1 |
splice_region_variant&intron_variant | LOW | c.1183-4A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134550059 | ||||||
| chr3:134550318
|
T | C | 7 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(4): Show | 7 | HG02630.hp1 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1380+58T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134550318 | ||||||
| chr3:134550396
|
A | G | 1 | a0001c0001t0002g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1380+136A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134550396 | ||||||
| chr3:134550543
|
G | T | 1 | a0001c0001t0004g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1380+283G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134550543 | ||||||
| chr3:134550545
|
T | A | 1 | a0001c0001t0004g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1380+285T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134550545 | ||||||
| chr3:134550547
|
G | A | 1 | a0001c0001t0004g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1380+287G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134550547 | ||||||
| chr3:134550548
|
C | A | 1 | a0001c0001t0004g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1380+288C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134550548 | ||||||
| chr3:134550665
|
CAAGTGGG others(8): Show |
C | 2 | a0001c0003t0001g0151a0002c0002t0001g0270 | 2 | NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1380+409_1380+423d others(17): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134550665 | |||||
| chr3:134550699
|
G | C | 211 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1380+439G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134550699 | ||||||
| chr3:134550800
|
G | C | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1380+540G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134550800 | ||||||
| chr3:134550958
|
A | T | 1 | a0007c0009t0001g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1380+698A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134550958 | ||||||
| chr3:134551181
|
AAT | A | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381-743_1381-742d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551181 | |||||
| chr3:134551231
|
G | A | 8 | a0001c0001t0005g0120a0001c0001t0005g0122a0001c0001t0005g0123others(5): Show | 8 | NA18940.hp2 NA18951.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.1381-695G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134551231 | ||||||
| chr3:134551286
|
A | G | 2 | a0002c0002t0001g0241a0002c0002t0001g0293 | 2 | NA18978.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1381-640A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134551286 | ||||||
| chr3:134551314
|
C | T | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1381-612C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134551314 | ||||||
| chr3:134551505
|
A | G | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1381-421A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134551505 | ||||||
| chr3:134551519
|
T | C | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381-407T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134551519 | ||||||
| chr3:134551626
|
T | C | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1381-300T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134551626 | ||||||
| chr3:134551724
|
CAT | C | 4 | a0001c0001t0004g0102a0001c0001t0004g0295a0001c0001t0013g0088others(1): Show | 4 | HG03017.hp1 HG03453.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1381-172_1381-171d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551724 | |||||
| chr3:134551724
|
CATAT | C | 22 | a0001c0001t0002g0053a0001c0001t0002g0071a0001c0001t0002g0101others(19): Show | 24 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.1381-174_1381-171d others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551724 | |||||
| chr3:134551724
|
CATATAT | C | 65 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(62): Show | 68 | HG00140.hp2 HG00738.hp2 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.1381-176_1381-171d others(8): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551724 | |||||
| chr3:134551724
|
CATATATA others(3): Show |
C | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1381-180_1381-171d others(12): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551724 | |||||
| chr3:134551724
|
CATATATA others(7): Show |
C | 1 | a0002c0002t0001g0284 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1381-184_1381-171d others(16): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551724 | |||||
| chr3:134551738
|
TATATATA others(11): Show |
T | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381-186_1381-169d others(20): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551738 | |||||
| chr3:134551740
|
TATATATA others(9): Show |
T | 83 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(80): Show | 85 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.1381-184_1381-169d others(18): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551740 | |||||
| chr3:134551742
|
TATATATA others(7): Show |
T | 101 | a0001c0001t0001g0008a0001c0001t0001g0211a0001c0001t0001g0221others(98): Show | 104 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1381-182_1381-169d others(16): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551742 | |||||
| chr3:134551744
|
TATATATA others(5): Show |
T | 13 | a0001c0001t0001g0216a0001c0001t0001g0286a0001c0001t0001g0287others(10): Show | 13 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.1381-180_1381-169d others(14): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551744 | |||||
| chr3:134551752
|
T | C | 1 | a0001c0001t0005g0126 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1381-174T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134551752 | ||||||
| chr3:134551754
|
T | C | 16 | a0001c0001t0002g0009a0001c0001t0002g0035a0001c0001t0002g0036others(13): Show | 16 | HG01106.hp2 HG01496.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1381-172T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134551754 | ||||||
| chr3:134551807
|
G | GTA | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.1381-108_1381-107d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551807 | |||||
| chr3:134552044
|
A | C | 46 | a0001c0003t0003g0154a0001c0003t0003g0155a0001c0003t0003g0156others(43): Show | 46 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.1467+32A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552044 | ||||||
| chr3:134552092
|
G | A | 1 | a0002c0002t0001g0242 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1467+80G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552092 | ||||||
| chr3:134552226
|
G | A | 2 | a0001c0003t0003g0160a0001c0003t0003g0176 | 2 | HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1467+214G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552226 | ||||||
| chr3:134552295
|
C | G | 90 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(87): Show | 95 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1467+283C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552295 | ||||||
| chr3:134552354
|
C | G | 4 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1467+342C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552354 | ||||||
| chr3:134552384
|
G | C | 1 | a0001c0001t0004g0019 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1467+372G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552384 | ||||||
| chr3:134552388
|
A | G | 6 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(3): Show | 6 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1467+376A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552388 | ||||||
| chr3:134552390
|
G | A | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1467+378G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552390 | ||||||
| chr3:134552432
|
A | G | 1 | a0001c0001t0009g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1467+420A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552432 | ||||||
| chr3:134552750
|
T | C | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.1467+738T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552750 | ||||||
| chr3:134552907
|
G | A | 19 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(16): Show | 19 | HG01169.hp1 HG01891.hp1 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.1467+895G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552907 | ||||||
| chr3:134552938
|
C | T | 1 | a0001c0001t0002g0059 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1467+926C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552938 | ||||||
| chr3:134553167
|
G | A | 6 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(3): Show | 6 | NA18941.hp2 NA18955.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.1467+1155G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553167 | ||||||
| chr3:134553214
|
G | A | 3 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107 | 3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1467+1202G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553214 | ||||||
| chr3:134553447
|
A | T | 1 | a0002c0002t0001g0248 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1467+1435A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553447 | ||||||
| chr3:134553518
|
G | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0054 | 4 | NA18949.hp1 NA18960.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.1467+1506G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553518 | ||||||
| chr3:134553566
|
T | C | 1 | a0001c0003t0003g0179 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1467+1554T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553566 | ||||||
| chr3:134553660
|
T | A | 16 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0021others(13): Show | 16 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1467+1648T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553660 | ||||||
| chr3:134553716
|
A | G | 1 | a0005c0013t0007g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1467+1704A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553716 | ||||||
| chr3:134553779
|
A | G | 211 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1467+1767A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553779 | ||||||
| chr3:134553874
|
G | A | 1 | a0001c0001t0002g0312 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1467+1862G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553874 | ||||||
| chr3:134553930
|
T | TAA | 308 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(305): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1467+1919_1467+192 others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134553930 | |||||
| chr3:134553941
|
C | T | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1467+1929C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553941 | ||||||
| chr3:134553943
|
A | G | 9 | a0001c0001t0005g0120a0001c0001t0005g0121a0001c0001t0005g0122others(6): Show | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.1467+1931A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553943 | ||||||
| chr3:134554018
|
C | G | 1 | a0002c0002t0001g0276 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1467+2006C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554018 | ||||||
| chr3:134554023
|
C | T | 1 | a0007c0009t0001g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1467+2011C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554023 | ||||||
| chr3:134554042
|
G | A | 310 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(307): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.1467+2030G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554042 | ||||||
| chr3:134554066
|
C | A | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1467+2054C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554066 | ||||||
| chr3:134554173
|
A | G | 304 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(301): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1467+2161A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554173 | ||||||
| chr3:134554185
|
A | G | 211 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1467+2173A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554185 | ||||||
| chr3:134554232
|
C | G | 1 | a0004c0007t0003g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1467+2220C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554232 | ||||||
| chr3:134554238
|
C | A | 1 | a0002c0002t0001g0244 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1467+2226C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554238 | ||||||
| chr3:134554268
|
G | A | 2 | a0001c0001t0019g0061a0001c0001t0020g0092 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1467+2256G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554268 | ||||||
| chr3:134554304
|
A | G | 192 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(189): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1467+2292A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554304 | ||||||
| chr3:134554471
|
C | T | 308 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(305): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1467+2459C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554471 | ||||||
| chr3:134554485
|
G | C | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1467+2473G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554485 | ||||||
| chr3:134554502
|
C | G | 1 | a0001c0003t0001g0150 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1467+2490C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554502 | ||||||
| chr3:134554655
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1467+2643C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554655 | ||||||
| chr3:134554684
|
C | G | 1 | a0001c0003t0003g0200 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1467+2672C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554684 | ||||||
| chr3:134554904
|
G | A | 1 | a0001c0001t0006g0081 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1467+2892G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554904 | ||||||
| chr3:134555116
|
C | T | 51 | a0001c0003t0003g0154a0001c0003t0003g0155a0001c0003t0003g0156others(48): Show | 52 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.1468-3026C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555116 | ||||||
| chr3:134555117
|
G | A | 15 | a0001c0001t0001g0211a0001c0001t0001g0221a0001c0001t0001g0264others(12): Show | 15 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1468-3025G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555117 | ||||||
| chr3:134555349
|
G | A | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1468-2793G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555349 | ||||||
| chr3:134555360
|
A | G | 3 | a0001c0001t0011g0109a0001c0001t0011g0110a0001c0001t0011g0111 | 3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1468-2782A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555360 | ||||||
| chr3:134555496
|
C | G | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1468-2646C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555496 | ||||||
| chr3:134555517
|
T | C | 1 | a0001c0003t0003g0179 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1468-2625T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555517 | ||||||
| chr3:134555563
|
C | T | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1468-2579C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555563 | ||||||
| chr3:134555646
|
A | G | 4 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265others(1): Show | 4 | HG01496.hp2 HG02280.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-2496A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555646 | ||||||
| chr3:134555811
|
G | A | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468-2331G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555811 | ||||||
| chr3:134555855
|
C | T | 304 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(301): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1468-2287C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555855 | ||||||
| chr3:134555878
|
A | G | 203 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(200): Show | 208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1468-2264A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555878 | ||||||
| chr3:134555969
|
G | A | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1468-2173G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555969 | ||||||
| chr3:134556068
|
C | T | 191 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(188): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1468-2074C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556068 | ||||||
| chr3:134556110
|
T | G | 12 | a0001c0001t0001g0211a0001c0001t0001g0221a0001c0001t0001g0263others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1468-2032T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556110 | ||||||
| chr3:134556276
|
G | T | 1 | a0002c0002t0001g0228 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1468-1866G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556276 | ||||||
| chr3:134556302
|
T | C | 1 | a0001c0001t0002g0018 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1468-1840T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556302 | ||||||
| chr3:134556303
|
A | G | 1 | a0002c0002t0001g0209 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1468-1839A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556303 | ||||||
| chr3:134556304
|
C | G | 1 | a0001c0001t0001g0288 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1468-1838C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556304 | ||||||
| chr3:134556384
|
G | A | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1468-1758G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556384 | ||||||
| chr3:134556453
|
G | C | 1 | a0003c0006t0001g0222 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1468-1689G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556453 | ||||||
| chr3:134556479
|
A | G | 1 | a0002c0002t0001g0103 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1468-1663A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556479 | ||||||
| chr3:134556502
|
A | G | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1468-1640A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556502 | ||||||
| chr3:134556518
|
A | T | 1 | a0001c0003t0001g0134 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1468-1624A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556518 | ||||||
| chr3:134556605
|
G | C | 9 | a0002c0002t0001g0214a0002c0002t0001g0223a0002c0002t0001g0238others(6): Show | 9 | HG00735.hp1 HG01099.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1468-1537G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556605 | ||||||
| chr3:134556759
|
G | C | 211 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1468-1383G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556759 | ||||||
| chr3:134556778
|
G | A | 1 | a0001c0003t0003g0169 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1468-1364G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556778 | ||||||
| chr3:134557252
|
A | G | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1468-890A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557252 | ||||||
| chr3:134557376
|
G | GT | 30 | a0001c0001t0002g0009a0001c0001t0002g0015a0001c0001t0002g0022others(27): Show | 31 | HG00544.hp2 HG01106.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1468-738dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | |||||
| chr3:134557376
|
G | GTTTTTTT others(2): Show |
11 | a0001c0003t0003g0155a0001c0003t0003g0170a0001c0003t0003g0184others(8): Show | 12 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.1468-746_1468-738d others(11): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | |||||
| chr3:134557376
|
G | GTTTTTTT others(3): Show |
34 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0003t0001g0141others(31): Show | 34 | HG00735.hp2 HG01106.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.1468-747_1468-738d others(12): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | |||||
| chr3:134557376
|
G | GTTTTTTT others(4): Show |
23 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0133others(20): Show | 23 | HG00423.hp1 HG00741.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.1468-748_1468-738d others(13): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | |||||
| chr3:134557376
|
G | GTTTTTTT others(5): Show |
10 | a0001c0001t0001g0137a0001c0001t0001g0148a0001c0001t0001g0149others(7): Show | 11 | HG02622.hp2 HG02809.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.1468-749_1468-738d others(14): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | |||||
| chr3:134557376
|
G | GTTTTTTT others(6): Show |
2 | a0001c0001t0001g0207a0001c0003t0001g0152 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1468-750_1468-738d others(15): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | |||||
| chr3:134557376
|
G | GTTTTTTT others(7): Show |
3 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0009g0099 | 3 | HG01891.hp1 HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1468-751_1468-738d others(16): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | |||||
| chr3:134557376
|
G | GTTTTTTT others(11): Show |
1 | a0001c0001t0001g0138 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1468-755_1468-738d others(20): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | |||||
| chr3:134557376
|
GT | G | 10 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0010others(7): Show | 12 | NA18955.hp2 NA18960.hp2 NA18965.hp2 others(9): Show |
intron_variant | MODIFIER | c.1468-738delT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | |||||
| chr3:134557376
|
GTTTT | G | 81 | a0002c0002t0001g0002a0002c0002t0001g0103a0002c0002t0001g0209others(78): Show | 83 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1468-741_1468-738d others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | |||||
| chr3:134557376
|
GTTTTTTT others(3): Show |
G | 16 | a0001c0001t0001g0008a0001c0001t0001g0216a0001c0001t0001g0286others(13): Show | 17 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.1468-747_1468-738d others(12): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | |||||
| chr3:134557376
|
GTTTTTTT others(4): Show |
G | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1468-748_1468-738d others(13): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | |||||
| chr3:134557382
|
T | G | 1 | a0001c0001t0021g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1468-760T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557382 | ||||||
| chr3:134557387
|
T | G | 2 | a0002c0002t0001g0234a0002c0002t0001g0262 | 2 | NA18998.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1468-755T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557387 | ||||||
| chr3:134557388
|
T | G | 79 | a0002c0002t0001g0002a0002c0002t0001g0103a0002c0002t0001g0209others(76): Show | 81 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1468-754T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557388 | ||||||
| chr3:134557404
|
T | A | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1468-738T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557404 | ||||||
| chr3:134557500
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1468-642C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557500 | ||||||
| chr3:134557623
|
C | G | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1468-519C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557623 | ||||||
| chr3:134557638
|
A | G | 7 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(4): Show | 7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468-504A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557638 | ||||||
| chr3:134557791
|
G | A | 6 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(3): Show | 6 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1468-351G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557791 | ||||||
| chr3:134557865
|
C | A | 1 | a0001c0001t0002g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1468-277C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557865 | ||||||
| chr3:134557963
|
A | G | 1 | a0002c0002t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1468-179A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557963 | ||||||
| chr3:134558353
|
A | AT | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1673+12dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr3 | 134558353 | |||||
| chr3:134558457
|
A | G | 1 | a0001c0001t0007g0113 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1673+110A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 13/14 | chr3 | 134558457 | ||||||
| chr3:134558459
|
G | A | 202 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0130others(199): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1673+112G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 13/14 | chr3 | 134558459 | ||||||
| chr3:134558485
|
A | G | 1 | a0001c0001t0024g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1673+138A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 13/14 | chr3 | 134558485 | ||||||
| chr3:134558558
|
A | G | 4 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1673+211A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 13/14 | chr3 | 134558558 | ||||||
| chr3:134558898
|
T | C | 83 | a0002c0002t0001g0002a0002c0002t0001g0103a0002c0002t0001g0209others(80): Show | 85 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1674-252T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 13/14 | chr3 | 134558898 | ||||||
| chr3:134558960
|
T | G | 8 | a0001c0001t0005g0120a0001c0001t0005g0122a0001c0001t0005g0123others(5): Show | 8 | NA18940.hp2 NA18951.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.1674-190T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 13/14 | chr3 | 134558960 | ||||||
| chr3:134559461
|
T | C | 4 | a0001c0001t0007g0113a0001c0001t0007g0114a0001c0001t0007g0115others(1): Show | 4 | HG02572.hp1 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1953+32T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134559461 | ||||||
| chr3:134559761
|
A | G | 1 | a0001c0001t0005g0121 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1953+332A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134559761 | ||||||
| chr3:134559803
|
G | A | 1 | a0002c0002t0001g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1953+374G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134559803 | ||||||
| chr3:134559863
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1953+434G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134559863 | ||||||
| chr3:134560225
|
A | G | 3 | a0001c0001t0012g0105a0001c0001t0012g0106a0001c0001t0012g0107 | 3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1953+796A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134560225 | ||||||
| chr3:134560275
|
C | T | 3 | a0001c0001t0010g0086a0001c0001t0010g0090a0001c0001t0010g0091 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1953+846C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134560275 | ||||||
| chr3:134560355
|
A | G | 93 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1953+926A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134560355 | ||||||
| chr3:134560437
|
C | T | 3 | a0001c0003t0008g0007a0001c0003t0008g0180a0001c0003t0008g0199 | 4 | HG01256.hp2 HG01258.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1954-940C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134560437 | ||||||
| chr3:134560529
|
G | A | 83 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(80): Show | 85 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.1954-848G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134560529 | ||||||
| chr3:134560729
|
A | G | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1954-648A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134560729 | ||||||
| chr3:134560835
|
A | G | 83 | a0002c0002t0001g0002a0002c0002t0001g0103a0002c0002t0001g0209others(80): Show | 85 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1954-542A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134560835 | ||||||
| chr3:134561315
|
G | A | 2 | a0001c0003t0003g0165a0008c0008t0003g0182 | 2 | HG02015.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1954-62G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134561315 |