| geneid | 153241 |
|---|---|
| ensemblid | ENSG00000168944.17 |
| hgncid | 26690 |
| symbol | CEP120 |
| name | centrosomal protein 120 |
| refseq_nuc | NM_001375405.1 |
| refseq_prot | NP_001362334.1 |
| ensembl_nuc | ENST00000306467.10 |
| ensembl_prot | ENSP00000303058.6 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 123344892 |
| end | 123423403 |
| strand | - |
| ver | v1.2 |
| region | chr5:123344892-123423403 |
| region5000 | chr5:123339892-123428403 |
| regionname0 | CEP120_chr5_123344892_123423403 |
| regionname5000 | CEP120_chr5_123339892_123428403 |
| 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 | 1/1 | 986 | 167 | 52 | 38 | 53 | 8 | 14 | 43 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0002 | 0/0 | 986 | 89 | 14 | 12 | 53 | 2 | 8 | 44 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0003 | 0/0 | 986 | 74 | 13 | 11 | 42 | 1 | 7 | 32 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0004 | 0/0 | 986 | 34 | 6 | 8 | 14 | 0 | 6 | 9 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0005 | 0/0 | 986 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0006 | 0/0 | 986 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0007 | 0/0 | 986 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0008 | 0/0 | 986 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0009 | 0/0 | 986 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0010 | 0/0 | 986 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| 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 | 1/1 | 2961 | 117 | 24 | 20 | 52 | 5 | 14 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| c0002 | 0/0 | 2961 | 82 | 13 | 12 | 47 | 2 | 8 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| c0003 | 0/0 | 2961 | 73 | 13 | 10 | 42 | 1 | 7 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| c0004 | 0/0 | 2961 | 34 | 6 | 8 | 14 | 0 | 6 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| c0005 | 0/0 | 2961 | 33 | 15 | 15 | 0 | 3 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| c0006 | 0/0 | 2961 | 14 | 11 | 3 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| c0007 | 0/0 | 2961 | 6 | 6 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| c0008 | 0/0 | 2961 | 4 | 0 | 0 | 4 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| c0009 | 0/0 | 2961 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| c0010 | 0/0 | 2961 | 2 | 1 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| c0011 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| c0012 | 0/0 | 2961 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| c0013 | 0/0 | 2961 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| c0014 | 0/0 | 2961 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| c0015 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| c0016 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| c0017 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| c0018 | 0/0 | 2961 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| c0019 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| 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 | 0/0 | 2033 | 156 | 27 | 23 | 88 | 3 | 15 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| t0002 | 1/1 | 2033 | 103 | 31 | 13 | 42 | 3 | 12 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| t0003 | 0/0 | 2033 | 55 | 23 | 10 | 14 | 2 | 6 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| t0004 | 0/0 | 2033 | 21 | 0 | 6 | 15 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| t0005 | 0/0 | 2033 | 21 | 6 | 13 | 0 | 2 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| t0006 | 0/0 | 2033 | 5 | 0 | 2 | 0 | 2 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| t0007 | 0/0 | 2033 | 3 | 2 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| t0008 | 0/0 | 2033 | 2 | 2 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| t0009 | 0/0 | 2033 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| t0010 | 0/0 | 2033 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| t0011 | 0/0 | 2033 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| t0012 | 0/0 | 2033 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| t0013 | 0/0 | 2033 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| t0014 | 0/0 | 2033 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| t0015 | 0/0 | 2033 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| t0016 | 0/0 | 2033 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| t0017 | 0/0 | 2033 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| t0018 | 0/0 | 2033 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| 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 | 0/1 | 9 | 0 | 3 | 2 | 0 | 3 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0002 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0003 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0008 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| 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 | 1/1 | 2961 | 117 | 24 | 20 | 52 | 5 | 14 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0005 | 0/0 | 2961 | 33 | 15 | 15 | 0 | 3 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0006 | 0/0 | 2961 | 14 | 11 | 3 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0011 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0013 | 0/0 | 2961 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0016 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0002c0002 | 0/0 | 2961 | 82 | 13 | 12 | 47 | 2 | 8 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0002c0008 | 0/0 | 2961 | 4 | 0 | 0 | 4 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0002c0009 | 0/0 | 2961 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0002c0015 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0003c0003 | 0/0 | 2961 | 73 | 13 | 10 | 42 | 1 | 7 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0003c0018 | 0/0 | 2961 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0004c0004 | 0/0 | 2961 | 34 | 6 | 8 | 14 | 0 | 6 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0005c0007 | 0/0 | 2961 | 6 | 6 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0006c0010 | 0/0 | 2961 | 2 | 1 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0007c0017 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0008c0012 | 0/0 | 2961 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0009c0014 | 0/0 | 2961 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0010c0019 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 1/1 | 4993 | 87 | 21 | 11 | 38 | 3 | 12 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0001t0004 | 0/0 | 4993 | 20 | 0 | 6 | 14 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0001t0006 | 0/0 | 4993 | 5 | 0 | 2 | 0 | 2 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0001t0007 | 0/0 | 4993 | 3 | 2 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0001t0011 | 0/0 | 4993 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0001t0012 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0005t0003 | 0/0 | 4993 | 13 | 9 | 2 | 0 | 2 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0005t0005 | 0/0 | 4993 | 20 | 6 | 13 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0006t0001 | 0/0 | 4993 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0006t0002 | 0/0 | 4993 | 8 | 6 | 2 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0006t0003 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0006t0008 | 0/0 | 4993 | 2 | 2 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0006t0009 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0006t0013 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0011t0002 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0013t0004 | 0/0 | 4993 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0001c0016t0002 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0002c0002t0001 | 0/0 | 4993 | 80 | 13 | 11 | 46 | 2 | 8 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0002c0002t0014 | 0/0 | 4993 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0002c0002t0018 | 0/0 | 4993 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0002c0008t0002 | 0/0 | 4993 | 4 | 0 | 0 | 4 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0002c0009t0001 | 0/0 | 4993 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0002c0009t0010 | 0/0 | 4993 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0002c0015t0001 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0003c0003t0001 | 0/0 | 4993 | 72 | 13 | 10 | 41 | 1 | 7 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0003c0003t0017 | 0/0 | 4993 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0003c0018t0001 | 0/0 | 4993 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0004c0004t0003 | 0/0 | 4993 | 34 | 6 | 8 | 14 | 0 | 6 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0005c0007t0003 | 0/0 | 4993 | 6 | 6 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0006c0010t0002 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0006c0010t0015 | 0/0 | 4993 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0007c0017t0002 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0008c0012t0016 | 0/0 | 4993 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0009c0014t0005 | 0/0 | 4993 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| a0010c0019t0003 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | copy fasta | chr5 | 123339892 | 123428403 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/1 | 9 | 0 | 3 | 2 | 0 | 3 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0008 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0006g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0006g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0006g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0006g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0007g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0007g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0011g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0012g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0002g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0008g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0009g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0013g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0011t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0013t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0016t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0014g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0018g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0008t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0008t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0008t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0008t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0009t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0009t0010g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0015t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0002 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0003 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0017g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0018t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0005c0007t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0005c0007t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0005c0007t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0005c0007t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0005c0007t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0005c0007t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0006c0010t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0006c0010t0015g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0007c0017t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0008c0012t0016g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0009c0014t0005g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0010c0019t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0009 | c0014 | t0005 | g0076 | EUR | GBR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0281 | EUR | GBR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00280 | hp1 | a0003 | c0003 | t0001 | g0003 | EUR | FIN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0262 | EUR | FIN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0200 | EUR | FIN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00323 | hp2 | a0001 | c0005 | t0005 | g0071 | EUR | FIN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00423 | hp1 | a0003 | c0003 | t0001 | g0133 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00438 | hp1 | a0002 | c0009 | t0010 | g0031 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00558 | hp2 | a0003 | c0003 | t0001 | g0301 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00597 | hp1 | a0003 | c0003 | t0001 | g0139 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00609 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00609 | hp2 | a0004 | c0004 | t0003 | g0100 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00621 | hp2 | a0003 | c0003 | t0001 | g0292 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0106 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0198 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00642 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00733 | hp1 | a0004 | c0004 | t0003 | g0015 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00735 | hp1 | a0004 | c0004 | t0003 | g0055 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0105 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00738 | hp1 | a0001 | c0005 | t0005 | g0080 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00741 | hp1 | a0001 | c0005 | t0005 | g0004 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01069 | hp1 | a0001 | c0006 | t0002 | g0207 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0104 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01070 | hp2 | a0004 | c0004 | t0003 | g0044 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01071 | hp1 | a0001 | c0006 | t0002 | g0006 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01071 | hp2 | a0004 | c0004 | t0003 | g0043 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01074 | hp2 | a0001 | c0005 | t0005 | g0066 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01081 | hp1 | a0002 | c0002 | t0014 | g0124 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0247 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0129 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01099 | hp2 | a0003 | c0018 | t0001 | g0304 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0107 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01167 | hp1 | a0001 | c0005 | t0005 | g0004 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01167 | hp2 | a0004 | c0004 | t0003 | g0013 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01168 | hp2 | a0001 | c0005 | t0005 | g0064 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01169 | hp1 | a0001 | c0005 | t0005 | g0072 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01192 | hp1 | a0001 | c0005 | t0005 | g0075 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01192 | hp2 | a0004 | c0004 | t0003 | g0013 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01243 | hp1 | a0006 | c0010 | t0015 | g0033 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0146 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01255 | hp1 | a0001 | c0005 | t0003 | g0091 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01255 | hp2 | a0001 | c0005 | t0003 | g0011 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01257 | hp1 | a0001 | c0006 | t0001 | g0103 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01257 | hp2 | a0001 | c0005 | t0005 | g0067 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01346 | hp1 | a0001 | c0005 | t0005 | g0074 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0271 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01358 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01361 | hp2 | a0001 | c0005 | t0005 | g0079 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01433 | hp1 | a0003 | c0003 | t0001 | g0305 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01496 | hp1 | a0001 | c0005 | t0005 | g0012 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01496 | hp2 | a0001 | c0001 | t0007 | g0325 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0244 | EUR | IBS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01515 | hp2 | a0001 | c0005 | t0003 | g0011 | EUR | IBS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0029 | EUR | IBS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01517 | hp2 | a0001 | c0005 | t0003 | g0081 | EUR | IBS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0110 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01884 | hp2 | a0003 | c0003 | t0001 | g0184 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01891 | hp1 | a0004 | c0004 | t0003 | g0061 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0192 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01943 | hp1 | a0003 | c0003 | t0001 | g0298 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01943 | hp2 | a0001 | c0005 | t0005 | g0012 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01952 | hp1 | a0004 | c0004 | t0003 | g0015 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0238 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01975 | hp2 | a0003 | c0003 | t0001 | g0306 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01981 | hp1 | a0004 | c0004 | t0003 | g0047 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0122 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02004 | hp1 | a0003 | c0003 | t0001 | g0297 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02004 | hp2 | a0001 | c0005 | t0005 | g0004 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02027 | hp2 | a0002 | c0002 | t0018 | g0328 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02040 | hp1 | a0004 | c0004 | t0003 | g0052 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0213 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02056 | hp2 | a0004 | c0004 | t0003 | g0051 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02071 | hp1 | a0003 | c0003 | t0001 | g0313 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02074 | hp2 | a0003 | c0003 | t0001 | g0101 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02080 | hp1 | a0003 | c0003 | t0001 | g0302 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0294 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02132 | hp1 | a0003 | c0003 | t0001 | g0309 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02145 | hp1 | a0005 | c0007 | t0003 | g0087 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0193 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02148 | hp2 | a0003 | c0003 | t0001 | g0307 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02165 | hp1 | a0003 | c0003 | t0001 | g0178 | EAS | CDX | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | CDX | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02257 | hp1 | a0001 | c0006 | t0002 | g0206 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02257 | hp2 | a0001 | c0005 | t0005 | g0036 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02258 | hp2 | a0001 | c0005 | t0003 | g0085 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02273 | hp1 | a0003 | c0003 | t0001 | g0183 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0253 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0317 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02280 | hp2 | a0004 | c0004 | t0003 | g0038 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02293 | hp1 | a0003 | c0003 | t0001 | g0002 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0278 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02451 | hp1 | a0001 | c0006 | t0002 | g0006 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0326 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02523 | hp2 | a0004 | c0004 | t0003 | g0097 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02572 | hp2 | a0003 | c0003 | t0001 | g0180 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02615 | hp1 | a0001 | c0005 | t0005 | g0078 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02615 | hp2 | a0003 | c0003 | t0001 | g0196 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0149 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0316 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0319 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0267 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0154 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02647 | hp2 | a0001 | c0005 | t0003 | g0092 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0299 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0112 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02698 | hp2 | a0003 | c0003 | t0001 | g0190 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02717 | hp1 | a0001 | c0001 | t0012 | g0274 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02717 | hp2 | a0006 | c0010 | t0002 | g0202 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02723 | hp1 | a0005 | c0007 | t0003 | g0086 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02738 | hp1 | a0003 | c0003 | t0001 | g0188 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02809 | hp1 | a0004 | c0004 | t0003 | g0059 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02809 | hp2 | a0003 | c0003 | t0001 | g0182 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0153 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02818 | hp2 | a0001 | c0005 | t0003 | g0096 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02886 | hp1 | a0001 | c0005 | t0003 | g0082 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0152 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02896 | hp1 | a0001 | c0005 | t0003 | g0090 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02965 | hp1 | a0003 | c0003 | t0001 | g0142 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02965 | hp2 | a0001 | c0005 | t0005 | g0070 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02970 | hp1 | a0007 | c0017 | t0002 | g0209 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02970 | hp2 | a0001 | c0005 | t0003 | g0323 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02976 | hp1 | a0001 | c0016 | t0002 | g0210 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02976 | hp2 | a0010 | c0019 | t0003 | g0108 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03017 | hp1 | a0001 | c0001 | t0011 | g0248 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0111 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03041 | hp1 | a0001 | c0006 | t0002 | g0205 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0315 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0327 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03098 | hp2 | a0003 | c0003 | t0001 | g0185 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03130 | hp1 | a0003 | c0003 | t0001 | g0187 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03130 | hp2 | a0002 | c0015 | t0001 | g0318 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03139 | hp1 | a0001 | c0005 | t0005 | g0068 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03195 | hp2 | a0001 | c0006 | t0013 | g0208 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0150 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0174 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03225 | hp1 | a0004 | c0004 | t0003 | g0058 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03239 | hp2 | a0004 | c0004 | t0003 | g0040 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0169 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0285 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03486 | hp1 | a0001 | c0006 | t0008 | g0010 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03486 | hp2 | a0005 | c0007 | t0003 | g0098 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03491 | hp1 | a0004 | c0004 | t0003 | g0045 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0017 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0017 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0199 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03516 | hp1 | a0001 | c0006 | t0003 | g0322 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03540 | hp2 | a0001 | c0006 | t0002 | g0204 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0151 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03654 | hp2 | a0008 | c0012 | t0016 | g0069 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0032 | SAS | STU | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0121 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03834 | hp1 | a0001 | c0001 | t0006 | g0290 | SAS | BEB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0003 | SAS | BEB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0201 | SAS | BEB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03942 | hp2 | a0004 | c0004 | t0003 | g0039 | SAS | BEB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG04115 | hp1 | a0004 | c0004 | t0003 | g0057 | SAS | STU | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0279 | SAS | STU | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0284 | SAS | BEB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG04184 | hp2 | a0004 | c0004 | t0003 | g0037 | SAS | BEB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG04199 | hp1 | a0004 | c0004 | t0003 | g0053 | SAS | STU | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG04199 | hp2 | a0003 | c0003 | t0001 | g0293 | SAS | STU | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG04204 | hp1 | a0003 | c0003 | t0001 | g0002 | SAS | STU | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | STU | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18522 | hp1 | a0004 | c0004 | t0003 | g0060 | AFR | YRI | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18522 | hp2 | a0001 | c0011 | t0002 | g0203 | AFR | YRI | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18612 | hp1 | a0004 | c0004 | t0003 | g0054 | EAS | CHB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | CHB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18906 | hp1 | a0003 | c0003 | t0001 | g0181 | AFR | YRI | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18906 | hp2 | a0001 | c0005 | t0003 | g0063 | AFR | YRI | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18939 | hp1 | a0003 | c0003 | t0001 | g0314 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0234 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18941 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18946 | hp1 | a0004 | c0004 | t0003 | g0046 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18949 | hp1 | a0001 | c0013 | t0004 | g0242 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18949 | hp2 | a0002 | c0008 | t0002 | g0217 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18950 | hp1 | a0002 | c0008 | t0002 | g0218 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18951 | hp2 | a0003 | c0003 | t0001 | g0310 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18952 | hp1 | a0003 | c0003 | t0001 | g0137 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18953 | hp2 | a0004 | c0004 | t0003 | g0048 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18956 | hp1 | a0003 | c0003 | t0001 | g0312 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0195 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18963 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18964 | hp1 | a0003 | c0003 | t0001 | g0176 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18966 | hp2 | a0002 | c0008 | t0002 | g0220 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18968 | hp1 | a0004 | c0004 | t0003 | g0041 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18972 | hp1 | a0003 | c0003 | t0001 | g0191 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18974 | hp2 | a0003 | c0003 | t0001 | g0022 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18977 | hp2 | a0003 | c0003 | t0001 | g0141 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18979 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18979 | hp2 | a0003 | c0003 | t0001 | g0173 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18980 | hp1 | a0003 | c0003 | t0001 | g0140 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18981 | hp1 | a0003 | c0003 | t0001 | g0021 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18982 | hp1 | a0004 | c0004 | t0003 | g0049 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18988 | hp2 | a0003 | c0003 | t0001 | g0295 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18990 | hp2 | a0004 | c0004 | t0003 | g0094 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18991 | hp1 | a0004 | c0004 | t0003 | g0056 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18993 | hp2 | a0003 | c0003 | t0001 | g0311 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18994 | hp2 | a0003 | c0003 | t0001 | g0189 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18995 | hp1 | a0003 | c0003 | t0001 | g0021 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19006 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19010 | hp2 | a0004 | c0004 | t0003 | g0062 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0211 | AFR | LWK | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19030 | hp2 | a0001 | c0005 | t0003 | g0084 | AFR | LWK | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | LWK | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19043 | hp2 | a0005 | c0007 | t0003 | g0099 | AFR | LWK | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19054 | hp1 | a0004 | c0004 | t0003 | g0050 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19054 | hp2 | a0003 | c0003 | t0017 | g0177 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19059 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19059 | hp2 | a0003 | c0003 | t0001 | g0194 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19060 | hp2 | a0003 | c0003 | t0001 | g0296 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19062 | hp2 | a0003 | c0003 | t0001 | g0020 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19065 | hp1 | a0003 | c0003 | t0001 | g0308 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19072 | hp1 | a0002 | c0008 | t0002 | g0219 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19079 | hp1 | a0003 | c0003 | t0001 | g0134 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19080 | hp1 | a0003 | c0003 | t0001 | g0115 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19081 | hp1 | a0003 | c0003 | t0001 | g0179 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19083 | hp1 | a0003 | c0003 | t0001 | g0135 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19084 | hp2 | a0002 | c0009 | t0001 | g0125 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19085 | hp2 | a0003 | c0003 | t0001 | g0136 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19087 | hp1 | a0003 | c0003 | t0001 | g0022 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19090 | hp1 | a0003 | c0003 | t0001 | g0020 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19091 | hp2 | a0004 | c0004 | t0003 | g0042 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA20129 | hp1 | a0001 | c0006 | t0002 | g0324 | AFR | ASW | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA20129 | hp2 | a0001 | c0006 | t0009 | g0030 | AFR | ASW | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0095 | EUR | TSI | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | TSI | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0255 | SAS | GIH | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA20905 | hp2 | a0003 | c0003 | t0001 | g0186 | SAS | GIH | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01123 | hp2 | a0003 | c0003 | t0001 | g0303 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02109 | hp1 | a0001 | c0005 | t0005 | g0073 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0212 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02486 | hp1 | a0001 | c0005 | t0005 | g0077 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02486 | hp2 | a0005 | c0007 | t0003 | g0089 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02559 | hp2 | a0001 | c0006 | t0008 | g0010 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03471 | hp2 | a0005 | c0007 | t0003 | g0088 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG06807 | hp1 | a0001 | c0006 | t0002 | g0006 | AFR | USA | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG06807 | hp2 | a0003 | c0003 | t0001 | g0291 | AFR | USA | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18955 | hp1 | a0003 | c0003 | t0001 | g0300 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA20300 | hp1 | a0004 | c0004 | t0003 | g0093 | AFR | USA | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA20300 | hp2 | a0001 | c0005 | t0003 | g0083 | AFR | USA | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA21309 | hp1 | a0003 | c0003 | t0001 | g0197 | AFR | LWK | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0321 | AFR | LWK | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0001 | REF | REF | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0065 | REF | REF | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:123346640
|
C | T | 2 | a0004a0010 | 35 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(32): Show |
missense_variant | MODERATE | c.2840G>A | p.Arg947His | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 3245/4993 | 2840/2961 | 947/986 | chr5 | 123346640 | ||
| chr5:123350033
|
C | G | 2 | a0003a0008 | 75 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(72): Show |
missense_variant | MODERATE | c.2637G>C | p.Gln879His | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/20 | 3042/4993 | 2637/2961 | 879/986 | chr5 | 123350033 | ||
| chr5:123377399
|
T | C | 1 | a0009 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.2333A>G | p.Glu778Gly | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/20 | 2738/4993 | 2333/2961 | 778/986 | chr5 | 123377399 | ||
| chr5:123378350
|
T | C | 2 | a0006a0007 | 3 | HG01243.hp1 HG02717.hp2 HG02970.hp1 |
missense_variant | MODERATE | c.2182A>G | p.Ser728Gly | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 15/20 | 2587/4993 | 2182/2961 | 728/986 | chr5 | 123378350 | ||
| chr5:123383042
|
G | C | 3 | a0002a0003a0010 | 164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
missense_variant | MODERATE | c.1804C>G | p.Leu602Val | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 12/20 | 2209/4993 | 1804/2961 | 602/986 | chr5 | 123383042 | ||
| chr5:123390074
|
G | A | 1 | a0005 | 6 | HG02145.hp1 HG02486.hp2 HG02723.hp1 others(3): Show |
missense_variant | MODERATE | c.1105C>T | p.Pro369Ser | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/20 | 1510/4993 | 1105/2961 | 369/986 | chr5 | 123390074 | ||
| chr5:123412500
|
T | C | 1 | a0006 | 2 | HG01243.hp1 HG02717.hp2 |
missense_variant | MODERATE | c.362A>G | p.Lys121Arg | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/20 | 767/4993 | 362/2961 | 121/986 | chr5 | 123412500 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:123346636
|
C | T | 1 | a0001c0013 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.2844G>A | p.Leu948Leu | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 3249/4993 | 2844/2961 | 948/986 | chr5 | 123346636 | ||
| chr5:123346654
|
A | G | 16 | a0001c0005a0001c0006a0001c0011others(13): Show | 254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
synonymous_variant | LOW | c.2826T>C | p.Asp942Asp | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 3231/4993 | 2826/2961 | 942/986 | chr5 | 123346654 | ||
| chr5:123378345
|
C | T | 1 | a0003c0018 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.2187G>A | p.Val729Val | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 15/20 | 2592/4993 | 2187/2961 | 729/986 | chr5 | 123378345 | ||
| chr5:123390105
|
C | T | 1 | a0001c0016 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.1074G>A | p.Glu358Glu | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/20 | 1479/4993 | 1074/2961 | 358/986 | chr5 | 123390105 | ||
| chr5:123391332
|
G | A | 11 | a0001c0006a0001c0011a0001c0016others(8): Show | 182 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(179): Show |
synonymous_variant | LOW | c.816C>T | p.His272His | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 7/20 | 1221/4993 | 816/2961 | 272/986 | chr5 | 123391332 | ||
| chr5:123412460
|
G | A | 1 | a0002c0009 | 2 | HG00438.hp1 NA19084.hp2 |
synonymous_variant | LOW | c.402C>T | p.Thr134Thr | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/20 | 807/4993 | 402/2961 | 134/986 | chr5 | 123412460 | ||
| chr5:123418373
|
C | T | 1 | a0001c0011 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.192G>A | p.Ala64Ala | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/20 | 597/4993 | 192/2961 | 64/986 | chr5 | 123418373 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:123344973
|
T | G | 3 | a0001c0005t0005a0008c0012t0016a0009c0014t0005 | 22 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1546A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 1546 | chr5 | 123344973 | |||||
| chr5:123344978
|
A | G | 2 | a0001c0001t0004a0001c0013t0004 | 21 | HG01433.hp2 HG01952.hp2 HG01975.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1541T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 1541 | chr5 | 123344978 | |||||
| chr5:123345070
|
C | A | 1 | a0001c0001t0011 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1449G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 1449 | chr5 | 123345070 | |||||
| chr5:123345536
|
G | C | 8 | a0001c0005t0003a0001c0005t0005a0001c0006t0003others(5): Show | 77 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*983C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 983 | chr5 | 123345536 | |||||
| chr5:123345585
|
T | G | 11 | a0001c0006t0001a0002c0002t0001a0002c0002t0014others(8): Show | 161 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*934A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 934 | chr5 | 123345585 | |||||
| chr5:123345640
|
T | C | 1 | a0001c0006t0008 | 2 | HG02559.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*879A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 879 | chr5 | 123345640 | |||||
| chr5:123345726
|
G | A | 1 | a0001c0001t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*793C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 793 | chr5 | 123345726 | |||||
| chr5:123345762
|
G | C | 1 | a0002c0002t0014 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*757C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 757 | chr5 | 123345762 | |||||
| chr5:123345840
|
A | T | 1 | a0001c0001t0006 | 5 | HG00280.hp2 HG01081.hp2 HG01346.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*679T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 679 | chr5 | 123345840 | |||||
| chr5:123345977
|
T | C | 1 | a0001c0006t0013 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*542A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 542 | chr5 | 123345977 | |||||
| chr5:123346140
|
C | T | 12 | a0001c0006t0001a0001c0006t0008a0001c0006t0009others(9): Show | 163 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*379G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 379 | chr5 | 123346140 | |||||
| chr5:123346168
|
T | C | 1 | a0003c0003t0017 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*351A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 351 | chr5 | 123346168 | |||||
| chr5:123346272
|
A | T | 2 | a0001c0006t0008a0001c0006t0009 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*247T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 247 | chr5 | 123346272 | |||||
| chr5:123346460
|
T | G | 21 | a0001c0005t0003a0001c0005t0005a0001c0006t0001others(18): Show | 241 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(238): Show |
3_prime_UTR_variant | MODIFIER | c.*59A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 59 | chr5 | 123346460 | |||||
| chr5:123423029
|
G | A | 1 | a0001c0001t0007 | 3 | HG01496.hp2 HG02451.hp2 HG03098.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-31C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/20 | chr5 | 123423029 | ||||||
| chr5:123423058
|
C | G | 1 | a0002c0009t0010 | 1 | HG00438.hp1 | 5_prime_UTR_variant | MODIFIER | c.-60G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/20 | 60 | chr5 | 123423058 | |||||
| chr5:123423275
|
G | A | 1 | a0002c0002t0018 | 1 | HG02027.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-277C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/20 | chr5 | 123423275 | ||||||
| chr5:123423311
|
C | T | 2 | a0001c0006t0008a0001c0006t0009 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
5_prime_UTR_variant | MODIFIER | c.-313G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/20 | 313 | chr5 | 123423311 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:123347118
|
G | A | 34 | a0001c0005t0003g0323a0004c0004t0003g0013a0004c0004t0003g0015others(31): Show | 36 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.2727-365C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347118 | ||||||
| chr5:123347155
|
A | G | 1 | a0001c0001t0002g0270 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2727-402T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347155 | ||||||
| chr5:123347178
|
T | G | 1 | a0001c0006t0008g0010 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2727-425A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347178 | ||||||
| chr5:123347194
|
G | T | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2727-441C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347194 | ||||||
| chr5:123347220
|
C | T | 2 | a0001c0005t0005g0012a0001c0005t0005g0073 | 3 | HG01496.hp1 HG01943.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2727-467G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347220 | ||||||
| chr5:123347255
|
G | A | 1 | a0002c0002t0001g0105 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2727-502C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347255 | ||||||
| chr5:123347318
|
A | T | 217 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(214): Show | 241 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.2727-565T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347318 | ||||||
| chr5:123347469
|
C | G | 229 | a0001c0001t0002g0321a0001c0005t0003g0011a0001c0005t0003g0063others(226): Show | 255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.2727-716G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347469 | ||||||
| chr5:123347771
|
G | A | 1 | a0003c0003t0001g0173 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2727-1018C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347771 | ||||||
| chr5:123347793
|
T | C | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2727-1040A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347793 | ||||||
| chr5:123347801
|
C | T | 2 | a0003c0003t0001g0196a0003c0003t0001g0197 | 2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2727-1048G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347801 | ||||||
| chr5:123347919
|
GCC | G | 22 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(19): Show | 26 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.2727-1168_2727-116 others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347919 | ||||||
| chr5:123347977
|
A | C | 144 | a0001c0006t0001g0103a0002c0002t0001g0005a0002c0002t0001g0016others(141): Show | 161 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.2727-1224T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347977 | ||||||
| chr5:123348139
|
T | C | 1 | a0002c0002t0001g0126 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2727-1386A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348139 | ||||||
| chr5:123348302
|
T | C | 146 | a0001c0006t0001g0103a0001c0006t0008g0010a0001c0006t0009g0030others(143): Show | 164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.2727-1549A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348302 | ||||||
| chr5:123348315
|
TATCTTTA others(152): Show |
T | 1 | a0002c0002t0001g0102 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2726+1470_2727-156 others(4): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348315 | ||||||
| chr5:123348437
|
A | G | 145 | a0001c0006t0001g0103a0001c0006t0008g0010a0001c0006t0009g0030others(142): Show | 163 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.2726+1507T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348437 | ||||||
| chr5:123348480
|
T | G | 1 | a0002c0002t0001g0102 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2726+1464A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348480 | ||||||
| chr5:123348526
|
G | T | 11 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(8): Show | 13 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2726+1418C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348526 | ||||||
| chr5:123348551
|
G | A | 228 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(225): Show | 254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2726+1393C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348551 | ||||||
| chr5:123348651
|
A | G | 1 | a0001c0001t0002g0282 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2726+1293T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348651 | ||||||
| chr5:123348652
|
G | T | 1 | a0002c0002t0001g0102 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2726+1292C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348652 | ||||||
| chr5:123348681
|
T | C | 1 | a0001c0001t0002g0282 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2726+1263A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348681 | ||||||
| chr5:123348870
|
G | C | 217 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(214): Show | 241 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.2726+1074C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348870 | ||||||
| chr5:123348883
|
A | G | 3 | a0002c0002t0001g0211a0002c0002t0001g0212a0002c0002t0001g0213 | 3 | HG02055.hp2 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2726+1061T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348883 | ||||||
| chr5:123348897
|
G | A | 1 | a0002c0002t0018g0328 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2726+1047C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348897 | ||||||
| chr5:123348919
|
T | C | 37 | a0001c0006t0001g0103a0002c0002t0001g0005a0002c0002t0001g0016others(34): Show | 42 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.2726+1025A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348919 | ||||||
| chr5:123349007
|
T | C | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2726+937A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349007 | ||||||
| chr5:123349068
|
C | T | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2726+876G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349068 | ||||||
| chr5:123349071
|
C | T | 36 | a0001c0006t0001g0103a0002c0002t0001g0005a0002c0002t0001g0016others(33): Show | 41 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.2726+873G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349071 | ||||||
| chr5:123349228
|
C | T | 1 | a0001c0005t0003g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2726+716G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349228 | ||||||
| chr5:123349383
|
A | G | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2726+561T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349383 | ||||||
| chr5:123349434
|
A | G | 146 | a0001c0006t0001g0103a0001c0006t0008g0010a0001c0006t0009g0030others(143): Show | 164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.2726+510T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349434 | ||||||
| chr5:123349539
|
A | C | 1 | a0002c0002t0001g0106 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2726+405T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349539 | ||||||
| chr5:123349594
|
T | A | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2726+350A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349594 | ||||||
| chr5:123349606
|
A | G | 3 | a0002c0002t0001g0163a0002c0002t0001g0168a0002c0002t0001g0172 | 3 | NA18964.hp2 NA19059.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.2726+338T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349606 | ||||||
| chr5:123349654
|
T | C | 147 | a0001c0006t0001g0103a0001c0006t0003g0322a0001c0006t0008g0010others(144): Show | 165 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.2726+290A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349654 | ||||||
| chr5:123349662
|
A | G | 9 | a0003c0003t0001g0115a0003c0003t0001g0133a0003c0003t0001g0134others(6): Show | 9 | HG00423.hp1 HG00597.hp1 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.2726+282T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349662 | ||||||
| chr5:123350212
|
CT | C | 187 | a0001c0001t0002g0321a0001c0005t0003g0011a0001c0005t0003g0063others(184): Show | 209 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.2581-124delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350212 | ||||||
| chr5:123350314
|
A | T | 1 | a0001c0001t0004g0253 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2581-225T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350314 | ||||||
| chr5:123350405
|
T | C | 36 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(33): Show | 40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2581-316A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350405 | ||||||
| chr5:123350564
|
A | T | 1 | a0002c0002t0001g0150 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2581-475T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350564 | ||||||
| chr5:123350575
|
C | A | 1 | a0001c0005t0003g0096 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2581-486G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350575 | ||||||
| chr5:123350578
|
C | T | 1 | a0003c0018t0001g0304 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2581-489G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350578 | ||||||
| chr5:123350739
|
C | G | 1 | a0001c0001t0002g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2581-650G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350739 | ||||||
| chr5:123350821
|
T | C | 2 | a0002c0002t0001g0200a0002c0002t0001g0201 | 2 | HG00323.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2581-732A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350821 | ||||||
| chr5:123350903
|
G | T | 8 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(5): Show | 10 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2581-814C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350903 | ||||||
| chr5:123350913
|
C | G | 1 | a0002c0002t0001g0150 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2581-824G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350913 | ||||||
| chr5:123350982
|
C | A | 7 | a0001c0005t0003g0082a0001c0005t0003g0083a0001c0005t0003g0084others(4): Show | 7 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2581-893G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350982 | ||||||
| chr5:123351131
|
A | G | 4 | a0001c0001t0004g0232a0001c0001t0004g0233a0001c0001t0004g0234others(1): Show | 4 | NA18941.hp1 NA18951.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.2581-1042T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123351131 | ||||||
| chr5:123351211
|
C | T | 4 | a0002c0002t0001g0095a0002c0002t0001g0198a0002c0002t0001g0200others(1): Show | 4 | HG00323.hp1 HG00642.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.2581-1122G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123351211 | ||||||
| chr5:123351222
|
A | G | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2581-1133T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123351222 | ||||||
| chr5:123351342
|
C | G | 2 | a0006c0010t0002g0202a0006c0010t0015g0033 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2581-1253G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123351342 | ||||||
| chr5:123351379
|
T | C | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2581-1290A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123351379 | ||||||
| chr5:123351769
|
TTC | T | 144 | a0001c0006t0001g0103a0001c0006t0008g0010a0001c0006t0009g0030others(141): Show | 162 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.2581-1682_2581-168 others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123351769 | ||||||
| chr5:123351925
|
C | A | 8 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(5): Show | 10 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2581-1836G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123351925 | ||||||
| chr5:123352008
|
A | G | 10 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2581-1919T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123352008 | ||||||
| chr5:123352496
|
A | G | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2581-2407T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123352496 | ||||||
| chr5:123352540
|
C | G | 146 | a0001c0006t0001g0103a0001c0006t0008g0010a0001c0006t0009g0030others(143): Show | 164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.2581-2451G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123352540 | ||||||
| chr5:123352623
|
G | A | 1 | a0002c0002t0001g0121 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2581-2534C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123352623 | ||||||
| chr5:123352722
|
G | A | 1 | a0001c0001t0011g0248 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2581-2633C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123352722 | ||||||
| chr5:123352731
|
T | C | 228 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(225): Show | 254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2581-2642A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123352731 | ||||||
| chr5:123352894
|
G | GATGCTAC others(5): Show |
229 | a0001c0001t0002g0321a0001c0005t0003g0011a0001c0005t0003g0063others(226): Show | 255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.2581-2806_2581-280 others(16): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123352894 | ||||||
| chr5:123352949
|
T | C | 1 | a0001c0006t0009g0030 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2581-2860A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123352949 | ||||||
| chr5:123353009
|
G | C | 1 | a0004c0004t0003g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2581-2920C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353009 | ||||||
| chr5:123353016
|
G | A | 1 | a0001c0001t0004g0025 | 2 | NA18994.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2581-2927C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353016 | ||||||
| chr5:123353033
|
C | T | 229 | a0001c0001t0002g0321a0001c0005t0003g0011a0001c0005t0003g0063others(226): Show | 255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.2581-2944G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353033 | ||||||
| chr5:123353052
|
A | C | 4 | a0001c0001t0002g0014a0001c0001t0002g0246a0001c0001t0002g0279others(1): Show | 5 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.2581-2963T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353052 | ||||||
| chr5:123353094
|
T | C | 1 | a0001c0001t0002g0279 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2581-3005A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353094 | ||||||
| chr5:123353175
|
A | C | 2 | a0002c0002t0001g0166a0002c0002t0001g0170 | 2 | NA19006.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2581-3086T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353175 | ||||||
| chr5:123353276
|
G | T | 1 | a0001c0005t0003g0090 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2581-3187C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353276 | ||||||
| chr5:123353410
|
C | A | 1 | a0001c0001t0004g0273 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2581-3321G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353410 | ||||||
| chr5:123353410
|
C | T | 2 | a0002c0002t0001g0153a0002c0002t0001g0169 | 2 | HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2581-3321G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353410 | ||||||
| chr5:123353520
|
G | A | 1 | a0002c0002t0001g0172 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2581-3431C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353520 | ||||||
| chr5:123353521
|
T | G | 1 | a0002c0002t0001g0172 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2581-3432A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353521 | ||||||
| chr5:123353521
|
T | TAAG | 227 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(224): Show | 253 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.2581-3435_2581-343 others(7): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353521 | ||||||
| chr5:123353727
|
C | T | 228 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(225): Show | 254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2581-3638G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353727 | ||||||
| chr5:123353790
|
A | G | 229 | a0001c0001t0002g0321a0001c0005t0003g0011a0001c0005t0003g0063others(226): Show | 255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.2581-3701T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353790 | ||||||
| chr5:123354086
|
A | G | 13 | a0001c0005t0003g0082a0001c0005t0003g0083a0001c0005t0003g0084others(10): Show | 13 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2581-3997T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354086 | ||||||
| chr5:123354300
|
G | A | 1 | a0001c0001t0002g0263 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2581-4211C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354300 | ||||||
| chr5:123354361
|
T | C | 1 | a0002c0008t0002g0219 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2581-4272A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354361 | ||||||
| chr5:123354435
|
T | C | 1 | a0003c0003t0001g0319 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2581-4346A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354435 | ||||||
| chr5:123354629
|
C | A | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2581-4540G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354629 | ||||||
| chr5:123354667
|
G | A | 3 | a0001c0001t0002g0024a0001c0001t0002g0228a0001c0001t0002g0288 | 4 | NA18990.hp1 NA19009.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.2581-4578C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354667 | ||||||
| chr5:123354693
|
T | C | 1 | a0001c0006t0009g0030 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2581-4604A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354693 | ||||||
| chr5:123354736
|
A | G | 1 | a0002c0002t0001g0211 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2581-4647T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354736 | ||||||
| chr5:123354775
|
GT | G | 228 | a0001c0001t0002g0321a0001c0005t0003g0011a0001c0005t0003g0063others(225): Show | 254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2581-4687delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354775 | ||||||
| chr5:123354785
|
T | A | 9 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(6): Show | 11 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2581-4696A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354785 | ||||||
| chr5:123354868
|
T | G | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2581-4779A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354868 | ||||||
| chr5:123354881
|
C | A | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2581-4792G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354881 | ||||||
| chr5:123354891
|
C | T | 13 | a0001c0005t0003g0082a0001c0005t0003g0083a0001c0005t0003g0084others(10): Show | 13 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2581-4802G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354891 | ||||||
| chr5:123354892
|
G | A | 1 | a0004c0004t0003g0050 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2581-4803C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354892 | ||||||
| chr5:123354915
|
C | T | 1 | a0001c0006t0002g0324 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2581-4826G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354915 | ||||||
| chr5:123354957
|
C | A | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2581-4868G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354957 | ||||||
| chr5:123355027
|
C | A | 13 | a0001c0005t0003g0082a0001c0005t0003g0083a0001c0005t0003g0084others(10): Show | 13 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2581-4938G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355027 | ||||||
| chr5:123355122
|
T | C | 1 | a0001c0001t0004g0249 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2581-5033A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355122 | ||||||
| chr5:123355195
|
T | C | 227 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(224): Show | 253 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.2581-5106A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355195 | ||||||
| chr5:123355247
|
C | T | 2 | a0003c0003t0001g0196a0003c0003t0001g0197 | 2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2581-5158G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355247 | ||||||
| chr5:123355284
|
C | A | 5 | a0002c0002t0001g0146a0002c0002t0001g0149a0002c0002t0001g0150others(2): Show | 5 | HG01243.hp2 HG02622.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2581-5195G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355284 | ||||||
| chr5:123355306
|
G | T | 13 | a0001c0001t0002g0231a0001c0006t0002g0006a0001c0006t0002g0204others(10): Show | 15 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.2581-5217C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355306 | ||||||
| chr5:123355308
|
G | A | 2 | a0004c0004t0003g0060a0004c0004t0003g0061 | 2 | HG01891.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2581-5219C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355308 | ||||||
| chr5:123355334
|
A | T | 1 | a0001c0001t0002g0245 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2581-5245T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355334 | ||||||
| chr5:123355471
|
C | T | 7 | a0001c0016t0002g0210a0002c0002t0001g0018a0002c0002t0001g0102others(4): Show | 8 | HG00597.hp2 HG02080.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.2581-5382G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355471 | ||||||
| chr5:123355520
|
G | A | 228 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(225): Show | 254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2581-5431C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355520 | ||||||
| chr5:123355561
|
T | G | 48 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(45): Show | 54 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.2581-5472A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355561 | ||||||
| chr5:123355574
|
T | C | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2581-5485A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355574 | ||||||
| chr5:123355874
|
T | A | 216 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(213): Show | 240 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.2581-5785A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355874 | ||||||
| chr5:123355876
|
A | G | 228 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(225): Show | 254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2581-5787T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355876 | ||||||
| chr5:123355892
|
G | A | 228 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(225): Show | 254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2581-5803C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355892 | ||||||
| chr5:123355920
|
G | T | 1 | a0001c0005t0003g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2581-5831C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355920 | ||||||
| chr5:123355971
|
G | A | 1 | a0002c0002t0001g0095 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2581-5882C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355971 | ||||||
| chr5:123355995
|
T | A | 1 | a0003c0003t0001g0293 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2581-5906A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355995 | ||||||
| chr5:123356028
|
A | G | 98 | a0002c0002t0001g0294a0003c0003t0001g0002a0003c0003t0001g0003others(95): Show | 111 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.2581-5939T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123356028 | ||||||
| chr5:123356143
|
G | C | 228 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(225): Show | 254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2581-6054C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123356143 | ||||||
| chr5:123356332
|
C | G | 1 | a0002c0002t0001g0095 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2581-6243G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123356332 | ||||||
| chr5:123356386
|
C | T | 145 | a0001c0006t0001g0103a0001c0006t0008g0010a0001c0006t0009g0030others(142): Show | 163 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.2581-6297G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123356386 | ||||||
| chr5:123356563
|
T | C | 1 | a0001c0006t0009g0030 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2581-6474A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123356563 | ||||||
| chr5:123356612
|
AATTTGTC | A | 144 | a0001c0006t0001g0103a0002c0002t0001g0005a0002c0002t0001g0016others(141): Show | 161 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.2581-6530_2581-652 others(11): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123356612 | ||||||
| chr5:123356660
|
A | G | 228 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(225): Show | 254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2581-6571T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123356660 | ||||||
| chr5:123356691
|
A | C | 229 | a0001c0001t0002g0250a0001c0005t0003g0011a0001c0005t0003g0063others(226): Show | 255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.2581-6602T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123356691 | ||||||
| chr5:123356959
|
G | GT | 177 | a0001c0006t0001g0103a0002c0002t0001g0005a0002c0002t0001g0016others(174): Show | 196 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.2581-6871dupA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123356959 | ||||||
| chr5:123357092
|
G | C | 36 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(33): Show | 40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2581-7003C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357092 | ||||||
| chr5:123357507
|
T | C | 1 | a0001c0001t0004g0266 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2580+6989A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357507 | ||||||
| chr5:123357592
|
AAAACCCT others(8): Show |
A | 1 | a0001c0005t0005g0077 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2580+6889_2580+690 others(19): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357592 | ||||||
| chr5:123357641
|
A | G | 8 | a0003c0003t0001g0115a0003c0003t0001g0133a0003c0003t0001g0134others(5): Show | 8 | HG00423.hp1 HG00597.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.2580+6855T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357641 | ||||||
| chr5:123357653
|
T | G | 1 | a0010c0019t0003g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2580+6843A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357653 | ||||||
| chr5:123357762
|
G | A | 228 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(225): Show | 254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2580+6734C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357762 | ||||||
| chr5:123357863
|
ACATCTGA others(7): Show |
A | 4 | a0003c0003t0001g0180a0003c0003t0001g0181a0003c0003t0001g0182others(1): Show | 4 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2580+6619_2580+663 others(18): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357863 | ||||||
| chr5:123357880
|
A | G | 4 | a0003c0003t0001g0180a0003c0003t0001g0181a0003c0003t0001g0182others(1): Show | 4 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2580+6616T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357880 | ||||||
| chr5:123357883
|
A | G | 228 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(225): Show | 254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2580+6613T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357883 | ||||||
| chr5:123357914
|
A | G | 1 | a0001c0006t0009g0030 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2580+6582T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357914 | ||||||
| chr5:123358092
|
T | C | 228 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(225): Show | 254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2580+6404A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358092 | ||||||
| chr5:123358156
|
A | G | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2580+6340T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358156 | ||||||
| chr5:123358173
|
A | ACTT | 6 | a0005c0007t0003g0086a0005c0007t0003g0087a0005c0007t0003g0088others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2580+6320_2580+632 others(7): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358173 | ||||||
| chr5:123358207
|
A | G | 228 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(225): Show | 254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2580+6289T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358207 | ||||||
| chr5:123358355
|
A | G | 5 | a0002c0002t0001g0156a0002c0002t0001g0158a0002c0002t0001g0159others(2): Show | 5 | NA18944.hp2 NA18948.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.2580+6141T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358355 | ||||||
| chr5:123358368
|
G | C | 42 | a0001c0006t0001g0103a0002c0002t0001g0005a0002c0002t0001g0016others(39): Show | 47 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.2580+6128C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358368 | ||||||
| chr5:123358694
|
T | TCA | 226 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(223): Show | 252 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.2580+5800_2580+580 others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358694 | ||||||
| chr5:123358717
|
G | A | 1 | a0002c0002t0001g0111 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2580+5779C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358717 | ||||||
| chr5:123358856
|
C | T | 1 | a0001c0001t0006g0244 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2580+5640G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358856 | ||||||
| chr5:123358907
|
T | G | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2580+5589A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358907 | ||||||
| chr5:123358983
|
A | G | 1 | a0001c0001t0002g0277 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2580+5513T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358983 | ||||||
| chr5:123359072
|
G | C | 229 | a0001c0001t0002g0321a0001c0005t0003g0011a0001c0005t0003g0063others(226): Show | 255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.2580+5424C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123359072 | ||||||
| chr5:123359337
|
A | G | 229 | a0001c0001t0002g0276a0001c0005t0003g0011a0001c0005t0003g0063others(226): Show | 255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.2580+5159T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123359337 | ||||||
| chr5:123359396
|
T | G | 2 | a0002c0002t0001g0174a0002c0002t0001g0175 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2580+5100A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123359396 | ||||||
| chr5:123359480
|
T | G | 1 | a0001c0001t0002g0254 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2580+5016A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123359480 | ||||||
| chr5:123359536
|
A | T | 2 | a0003c0003t0001g0196a0003c0003t0001g0197 | 2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2580+4960T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123359536 | ||||||
| chr5:123360105
|
T | G | 1 | a0001c0001t0002g0230 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2580+4391A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360105 | ||||||
| chr5:123360129
|
CACAA | C | 34 | a0001c0006t0001g0103a0002c0002t0001g0005a0002c0002t0001g0016others(31): Show | 39 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.2580+4363_2580+436 others(8): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360129 | ||||||
| chr5:123360296
|
C | T | 2 | a0003c0003t0001g0196a0003c0003t0001g0197 | 2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2580+4200G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360296 | ||||||
| chr5:123360387
|
A | G | 1 | a0002c0002t0001g0118 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2580+4109T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360387 | ||||||
| chr5:123360605
|
C | G | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2580+3891G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360605 | ||||||
| chr5:123360653
|
G | GCAAGAGG others(12): Show |
144 | a0001c0006t0001g0103a0001c0006t0008g0010a0001c0006t0009g0030others(141): Show | 162 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.2580+3824_2580+384 others(23): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360653 | ||||||
| chr5:123360673
|
A | C | 230 | a0001c0001t0002g0250a0001c0001t0002g0321a0001c0005t0003g0011others(227): Show | 256 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.2580+3823T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360673 | ||||||
| chr5:123360697
|
G | T | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2580+3799C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360697 | ||||||
| chr5:123360774
|
G | C | 34 | a0001c0001t0002g0250a0001c0005t0003g0323a0004c0004t0003g0013others(31): Show | 36 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.2580+3722C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360774 | ||||||
| chr5:123360780
|
C | T | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2580+3716G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360780 | ||||||
| chr5:123360811
|
C | G | 3 | a0001c0001t0002g0215a0001c0001t0002g0243a0001c0001t0002g0277 | 3 | NA18968.hp2 NA18977.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2580+3685G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360811 | ||||||
| chr5:123360812
|
T | TAC | 4 | a0002c0002t0001g0114a0002c0002t0001g0128a0002c0002t0001g0138others(1): Show | 4 | NA18969.hp1 NA18987.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.2580+3682_2580+368 others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360812 | ||||||
| chr5:123360859
|
G | A | 3 | a0002c0002t0001g0113a0002c0009t0001g0125a0002c0009t0010g0031 | 3 | HG00438.hp1 NA18984.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.2580+3637C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360859 | ||||||
| chr5:123360900
|
A | G | 2 | a0001c0005t0003g0011a0001c0005t0003g0081 | 3 | HG01255.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2580+3596T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360900 | ||||||
| chr5:123360940
|
A | G | 1 | a0002c0002t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2580+3556T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360940 | ||||||
| chr5:123361031
|
A | ATAAT | 233 | a0001c0001t0002g0250a0001c0005t0003g0011a0001c0005t0003g0063others(230): Show | 259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.2580+3461_2580+346 others(8): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123361031 | ||||||
| chr5:123361049
|
A | G | 233 | a0001c0001t0002g0250a0001c0005t0003g0011a0001c0005t0003g0063others(230): Show | 259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.2580+3447T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123361049 | ||||||
| chr5:123361188
|
G | T | 230 | a0001c0001t0002g0250a0001c0001t0002g0321a0001c0005t0003g0011others(227): Show | 256 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.2580+3308C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123361188 | ||||||
| chr5:123361281
|
G | A | 2 | a0002c0002t0001g0143a0002c0002t0001g0144 | 2 | NA18960.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.2580+3215C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123361281 | ||||||
| chr5:123361315
|
T | C | 36 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(33): Show | 40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2580+3181A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123361315 | ||||||
| chr5:123361416
|
G | C | 1 | a0002c0002t0001g0164 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2580+3080C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123361416 | ||||||
| chr5:123361601
|
C | G | 36 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(33): Show | 40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2580+2895G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123361601 | ||||||
| chr5:123361737
|
C | T | 22 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(19): Show | 26 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.2580+2759G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123361737 | ||||||
| chr5:123361764
|
G | A | 35 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(32): Show | 39 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.2580+2732C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123361764 | ||||||
| chr5:123362198
|
T | C | 3 | a0003c0003t0001g0003a0003c0003t0001g0299a0003c0003t0001g0303 | 6 | HG00280.hp1 HG00642.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.2580+2298A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123362198 | ||||||
| chr5:123362299
|
G | A | 1 | a0002c0002t0001g0294 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2580+2197C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123362299 | ||||||
| chr5:123362438
|
A | T | 1 | a0001c0005t0005g0070 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2580+2058T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123362438 | ||||||
| chr5:123362661
|
A | C | 2 | a0001c0006t0008g0010a0001c0006t0009g0030 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2580+1835T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123362661 | ||||||
| chr5:123362673
|
G | A | 222 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(219): Show | 246 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.2580+1823C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123362673 | ||||||
| chr5:123362695
|
C | T | 233 | a0001c0001t0002g0321a0001c0005t0003g0011a0001c0005t0003g0063others(230): Show | 259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.2580+1801G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123362695 | ||||||
| chr5:123362839
|
A | G | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2580+1657T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123362839 | ||||||
| chr5:123362944
|
T | A | 1 | a0001c0005t0003g0323 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2580+1552A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123362944 | ||||||
| chr5:123363001
|
T | A | 35 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(32): Show | 39 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.2580+1495A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363001 | ||||||
| chr5:123363075
|
C | T | 1 | a0001c0001t0002g0282 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2580+1421G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363075 | ||||||
| chr5:123363227
|
A | G | 1 | a0003c0003t0001g0186 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2580+1269T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363227 | ||||||
| chr5:123363228
|
T | C | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2580+1268A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363228 | ||||||
| chr5:123363422
|
C | T | 1 | a0001c0005t0005g0068 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2580+1074G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363422 | ||||||
| chr5:123363491
|
G | A | 1 | a0002c0002t0001g0129 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2580+1005C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363491 | ||||||
| chr5:123363504
|
C | CTA | 182 | a0001c0001t0002g0250a0001c0006t0001g0103a0002c0002t0001g0005others(179): Show | 201 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.2580+990_2580+991d others(4): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363504 | ||||||
| chr5:123363583
|
T | G | 1 | a0001c0001t0012g0274 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2580+913A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363583 | ||||||
| chr5:123363643
|
C | G | 1 | a0001c0001t0002g0235 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2580+853G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363643 | ||||||
| chr5:123363731
|
T | C | 233 | a0001c0001t0002g0250a0001c0005t0003g0011a0001c0005t0003g0063others(230): Show | 259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.2580+765A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363731 | ||||||
| chr5:123363795
|
T | C | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2580+701A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363795 | ||||||
| chr5:123363909
|
T | C | 2 | a0003c0003t0001g0180a0003c0003t0001g0181 | 2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2580+587A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363909 | ||||||
| chr5:123364118
|
T | G | 68 | a0002c0002t0001g0118a0002c0002t0001g0294a0002c0008t0002g0217others(65): Show | 79 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.2580+378A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123364118 | ||||||
| chr5:123364684
|
A | G | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2482-90T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123364684 | ||||||
| chr5:123364709
|
C | T | 1 | a0002c0002t0001g0157 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2482-115G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123364709 | ||||||
| chr5:123364929
|
C | A | 1 | a0001c0001t0002g0251 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2482-335G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123364929 | ||||||
| chr5:123364962
|
T | C | 151 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(148): Show | 169 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.2482-368A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123364962 | ||||||
| chr5:123365112
|
T | C | 3 | a0003c0003t0001g0184a0003c0003t0001g0185a0003c0003t0001g0192 | 3 | HG01884.hp2 HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2482-518A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123365112 | ||||||
| chr5:123365234
|
G | GA | 233 | a0001c0001t0002g0321a0001c0005t0003g0011a0001c0005t0003g0063others(230): Show | 259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.2482-641dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123365234 | ||||||
| chr5:123365540
|
A | G | 23 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(20): Show | 27 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.2482-946T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123365540 | ||||||
| chr5:123365579
|
T | G | 2 | a0004c0004t0003g0058a0004c0004t0003g0059 | 2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2482-985A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123365579 | ||||||
| chr5:123365822
|
T | G | 2 | a0002c0002t0001g0200a0002c0002t0001g0201 | 2 | HG00323.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2482-1228A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123365822 | ||||||
| chr5:123365867
|
T | C | 233 | a0001c0001t0002g0321a0001c0005t0003g0011a0001c0005t0003g0063others(230): Show | 259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.2482-1273A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123365867 | ||||||
| chr5:123366005
|
TCACACTA others(8): Show |
T | 232 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(229): Show | 258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.2482-1426_2482-141 others(19): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123366005 | ||||||
| chr5:123366317
|
A | G | 76 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(73): Show | 84 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.2482-1723T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123366317 | ||||||
| chr5:123366471
|
G | A | 2 | a0001c0001t0002g0237a0001c0001t0002g0321 | 2 | HG03654.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2482-1877C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123366471 | ||||||
| chr5:123366600
|
T | C | 233 | a0001c0001t0002g0321a0001c0005t0003g0011a0001c0005t0003g0063others(230): Show | 259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.2482-2006A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123366600 | ||||||
| chr5:123366644
|
A | G | 230 | a0001c0001t0002g0321a0001c0005t0003g0011a0001c0005t0003g0063others(227): Show | 256 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.2482-2050T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123366644 | ||||||
| chr5:123366880
|
G | T | 17 | a0001c0005t0005g0004a0001c0005t0005g0012a0001c0005t0005g0036others(14): Show | 20 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.2482-2286C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123366880 | ||||||
| chr5:123366881
|
A | T | 17 | a0001c0005t0005g0004a0001c0005t0005g0012a0001c0005t0005g0036others(14): Show | 20 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.2482-2287T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123366881 | ||||||
| chr5:123366882
|
A | G | 17 | a0001c0005t0005g0004a0001c0005t0005g0012a0001c0005t0005g0036others(14): Show | 20 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.2482-2288T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123366882 | ||||||
| chr5:123366883
|
A | T | 17 | a0001c0005t0005g0004a0001c0005t0005g0012a0001c0005t0005g0036others(14): Show | 20 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.2482-2289T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123366883 | ||||||
| chr5:123367068
|
T | G | 232 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(229): Show | 258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.2482-2474A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367068 | ||||||
| chr5:123367072
|
T | G | 156 | a0001c0006t0001g0103a0001c0006t0008g0010a0001c0006t0009g0030others(153): Show | 174 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.2482-2478A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367072 | ||||||
| chr5:123367214
|
C | T | 2 | a0003c0003t0001g0196a0003c0003t0001g0197 | 2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2482-2620G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367214 | ||||||
| chr5:123367227
|
A | C | 1 | a0001c0001t0004g0232 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2482-2633T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367227 | ||||||
| chr5:123367264
|
T | G | 8 | a0001c0006t0008g0010a0001c0006t0009g0030a0005c0007t0003g0086others(5): Show | 9 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2482-2670A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367264 | ||||||
| chr5:123367315
|
A | G | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2482-2721T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367315 | ||||||
| chr5:123367332
|
C | A | 221 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(218): Show | 245 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.2482-2738G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367332 | ||||||
| chr5:123367414
|
A | ATATG | 3 | a0003c0003t0001g0184a0003c0003t0001g0185a0003c0003t0001g0192 | 3 | HG01884.hp2 HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2482-2824_2482-282 others(8): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367414 | ||||||
| chr5:123367535
|
C | T | 5 | a0001c0006t0002g0006a0001c0006t0002g0206a0001c0006t0002g0207others(2): Show | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2482-2941G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367535 | ||||||
| chr5:123367578
|
A | C | 232 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(229): Show | 258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.2482-2984T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367578 | ||||||
| chr5:123367866
|
T | G | 5 | a0002c0002t0001g0156a0002c0002t0001g0158a0002c0002t0001g0159others(2): Show | 5 | NA18944.hp2 NA18948.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.2482-3272A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367866 | ||||||
| chr5:123367890
|
G | A | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2482-3296C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367890 | ||||||
| chr5:123367903
|
T | G | 2 | a0003c0003t0001g0180a0003c0003t0001g0181 | 2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2482-3309A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367903 | ||||||
| chr5:123368326
|
A | T | 222 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(219): Show | 246 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.2482-3732T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123368326 | ||||||
| chr5:123368375
|
T | C | 1 | a0002c0002t0001g0165 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2482-3781A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123368375 | ||||||
| chr5:123368428
|
G | A | 33 | a0001c0005t0003g0323a0004c0004t0003g0013a0004c0004t0003g0015others(30): Show | 35 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2482-3834C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123368428 | ||||||
| chr5:123368431
|
T | C | 1 | a0001c0005t0005g0079 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2482-3837A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123368431 | ||||||
| chr5:123368445
|
A | G | 1 | a0003c0003t0001g0189 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2482-3851T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123368445 | ||||||
| chr5:123368648
|
G | T | 28 | a0004c0004t0003g0013a0004c0004t0003g0015a0004c0004t0003g0037others(25): Show | 30 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.2481+4002C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123368648 | ||||||
| chr5:123368732
|
A | G | 232 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(229): Show | 258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.2481+3918T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123368732 | ||||||
| chr5:123368858
|
A | G | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2481+3792T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123368858 | ||||||
| chr5:123368955
|
C | T | 221 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(218): Show | 245 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.2481+3695G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123368955 | ||||||
| chr5:123369236
|
A | G | 1 | a0002c0002t0018g0328 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2481+3414T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369236 | ||||||
| chr5:123369416
|
A | G | 231 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(228): Show | 257 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.2481+3234T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369416 | ||||||
| chr5:123369550
|
C | T | 33 | a0001c0005t0003g0323a0004c0004t0003g0013a0004c0004t0003g0015others(30): Show | 35 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2481+3100G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369550 | ||||||
| chr5:123369627
|
A | G | 230 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(227): Show | 256 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.2481+3023T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369627 | ||||||
| chr5:123369637
|
T | C | 2 | a0001c0006t0008g0010a0001c0006t0009g0030 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2481+3013A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369637 | ||||||
| chr5:123369687
|
T | C | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2963A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369687 | ||||||
| chr5:123369690
|
T | A | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2960A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369690 | ||||||
| chr5:123369693
|
A | T | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2957T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369693 | ||||||
| chr5:123369703
|
C | G | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2947G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369703 | ||||||
| chr5:123369704
|
C | G | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2946G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369704 | ||||||
| chr5:123369709
|
C | G | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2941G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369709 | ||||||
| chr5:123369710
|
C | G | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2940G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369710 | ||||||
| chr5:123369716
|
A | T | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2934T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369716 | ||||||
| chr5:123369719
|
T | A | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2931A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369719 | ||||||
| chr5:123369722
|
G | A | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2928C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369722 | ||||||
| chr5:123369749
|
T | A | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2901A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369749 | ||||||
| chr5:123369753
|
T | C | 4 | a0002c0002t0001g0018a0002c0002t0001g0117a0002c0002t0001g0121others(1): Show | 5 | HG00597.hp2 HG02080.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.2481+2897A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369753 | ||||||
| chr5:123369841
|
C | T | 69 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(66): Show | 75 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.2481+2809G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369841 | ||||||
| chr5:123369922
|
A | G | 8 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(5): Show | 10 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2481+2728T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369922 | ||||||
| chr5:123370043
|
C | A | 218 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(215): Show | 241 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.2481+2607G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370043 | ||||||
| chr5:123370177
|
G | C | 1 | a0001c0001t0002g0286 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2481+2473C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370177 | ||||||
| chr5:123370471
|
C | T | 2 | a0001c0001t0002g0260a0001c0001t0002g0269 | 2 | HG02055.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2481+2179G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370471 | ||||||
| chr5:123370471
|
CTTTG | C | 15 | a0001c0005t0005g0004a0001c0005t0005g0012a0001c0005t0005g0036others(12): Show | 18 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.2481+2175_2481+217 others(8): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370471 | ||||||
| chr5:123370609
|
C | A | 1 | a0002c0002t0001g0160 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2481+2041G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370609 | ||||||
| chr5:123370671
|
A | ATG | 13 | a0001c0005t0003g0082a0001c0005t0003g0083a0001c0005t0003g0084others(10): Show | 13 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2481+1977_2481+197 others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370671 | ||||||
| chr5:123370677
|
G | GTA | 10 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2481+1972_2481+197 others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370677 | ||||||
| chr5:123370685
|
G | A | 2 | a0004c0004t0003g0058a0004c0004t0003g0059 | 2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2481+1965C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370685 | ||||||
| chr5:123370685
|
G | GTA | 205 | a0001c0005t0003g0063a0001c0005t0003g0096a0001c0005t0003g0323others(202): Show | 228 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.2481+1963_2481+196 others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370685 | ||||||
| chr5:123370685
|
G | GTATA | 2 | a0001c0005t0003g0011a0001c0005t0003g0081 | 3 | HG01255.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2481+1961_2481+196 others(8): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370685 | ||||||
| chr5:123370750
|
A | ATATATAT others(13): Show |
2 | a0001c0006t0008g0010a0001c0006t0009g0030 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2481+1880_2481+189 others(24): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370750 | ||||||
| chr5:123371055
|
T | C | 1 | a0001c0001t0002g0286 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2481+1595A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123371055 | ||||||
| chr5:123371193
|
T | C | 1 | a0001c0005t0003g0091 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2481+1457A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123371193 | ||||||
| chr5:123371231
|
G | C | 2 | a0001c0006t0008g0010a0001c0006t0009g0030 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2481+1419C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123371231 | ||||||
| chr5:123371239
|
G | T | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2481+1411C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123371239 | ||||||
| chr5:123371428
|
A | C | 1 | a0002c0002t0001g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2481+1222T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123371428 | ||||||
| chr5:123371441
|
C | T | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2481+1209G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123371441 | ||||||
| chr5:123371510
|
T | G | 4 | a0004c0004t0003g0058a0004c0004t0003g0059a0004c0004t0003g0060others(1): Show | 4 | HG01891.hp1 HG02809.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2481+1140A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123371510 | ||||||
| chr5:123371754
|
C | T | 1 | a0001c0005t0005g0077 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2481+896G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123371754 | ||||||
| chr5:123371814
|
A | C | 1 | a0002c0002t0001g0162 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2481+836T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123371814 | ||||||
| chr5:123372002
|
A | G | 1 | a0002c0002t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2481+648T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372002 | ||||||
| chr5:123372029
|
T | C | 1 | a0003c0003t0001g0181 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2481+621A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372029 | ||||||
| chr5:123372190
|
C | G | 13 | a0001c0005t0003g0082a0001c0005t0003g0083a0001c0005t0003g0084others(10): Show | 13 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2481+460G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372190 | ||||||
| chr5:123372192
|
C | T | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2481+458G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372192 | ||||||
| chr5:123372296
|
G | A | 2 | a0006c0010t0002g0202a0006c0010t0015g0033 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2481+354C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372296 | ||||||
| chr5:123372301
|
C | T | 1 | a0001c0001t0002g0014 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2481+349G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372301 | ||||||
| chr5:123372321
|
C | T | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+329G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372321 | ||||||
| chr5:123372510
|
G | A | 1 | a0002c0002t0001g0294 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2481+140C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372510 | ||||||
| chr5:123372579
|
T | A | 4 | a0004c0004t0003g0058a0004c0004t0003g0059a0004c0004t0003g0060others(1): Show | 4 | HG01891.hp1 HG02809.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2481+71A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372579 | ||||||
| chr5:123372583
|
C | T | 1 | a0001c0005t0003g0323 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2481+67G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372583 | ||||||
| chr5:123372780
|
A | T | 1 | a0003c0003t0001g0135 | 1 | NA19083.hp1 | splice_region_variant&intron_variant | LOW | c.2359-8T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123372780 | ||||||
| chr5:123372903
|
A | C | 2 | a0002c0002t0001g0155a0002c0002t0001g0167 | 2 | NA18967.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.2359-131T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123372903 | ||||||
| chr5:123373124
|
A | C | 1 | a0001c0001t0002g0029 | 2 | HG01109.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2359-352T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373124 | ||||||
| chr5:123373137
|
G | C | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2359-365C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373137 | ||||||
| chr5:123373228
|
G | A | 4 | a0003c0003t0001g0295a0003c0003t0001g0301a0003c0003t0001g0302others(1): Show | 4 | HG00558.hp2 HG02071.hp1 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2359-456C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373228 | ||||||
| chr5:123373428
|
G | C | 1 | a0001c0005t0003g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2359-656C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373428 | ||||||
| chr5:123373559
|
A | G | 1 | a0002c0002t0001g0119 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2359-787T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373559 | ||||||
| chr5:123373633
|
A | T | 148 | a0001c0006t0001g0103a0002c0002t0001g0005a0002c0002t0001g0016others(145): Show | 165 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.2359-861T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373633 | ||||||
| chr5:123373665
|
T | C | 1 | a0001c0005t0003g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2359-893A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373665 | ||||||
| chr5:123373668
|
C | T | 13 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0002g0214others(10): Show | 15 | HG01496.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2359-896G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373668 | ||||||
| chr5:123373678
|
T | C | 1 | a0003c0003t0001g0186 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2359-906A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373678 | ||||||
| chr5:123373703
|
C | T | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2359-931G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373703 | ||||||
| chr5:123373728
|
C | T | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2359-956G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373728 | ||||||
| chr5:123373740
|
A | G | 2 | a0001c0006t0008g0010a0001c0006t0009g0030 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2359-968T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373740 | ||||||
| chr5:123373935
|
C | T | 163 | a0001c0006t0001g0103a0001c0006t0002g0006a0001c0006t0002g0204others(160): Show | 183 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.2359-1163G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373935 | ||||||
| chr5:123374476
|
A | G | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2359-1704T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123374476 | ||||||
| chr5:123374556
|
T | G | 199 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(196): Show | 223 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.2359-1784A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123374556 | ||||||
| chr5:123374732
|
T | C | 1 | a0002c0002t0001g0129 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2359-1960A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123374732 | ||||||
| chr5:123375054
|
A | T | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2359-2282T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375054 | ||||||
| chr5:123375154
|
G | A | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2358+2220C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375154 | ||||||
| chr5:123375330
|
C | CT | 36 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(33): Show | 40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2358+2043dupA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375330 | ||||||
| chr5:123375341
|
G | A | 36 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(33): Show | 40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2358+2033C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375341 | ||||||
| chr5:123375474
|
C | T | 33 | a0001c0005t0003g0323a0004c0004t0003g0013a0004c0004t0003g0015others(30): Show | 35 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2358+1900G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375474 | ||||||
| chr5:123375582
|
G | A | 3 | a0006c0010t0002g0202a0006c0010t0015g0033a0007c0017t0002g0209 | 3 | HG01243.hp1 HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2358+1792C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375582 | ||||||
| chr5:123375588
|
GTTGGGAT others(1): Show |
G | 150 | a0001c0006t0001g0103a0001c0006t0008g0010a0001c0006t0009g0030others(147): Show | 168 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.2358+1778_2358+178 others(12): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375588 | ||||||
| chr5:123375597
|
A | G | 150 | a0001c0006t0001g0103a0001c0006t0008g0010a0001c0006t0009g0030others(147): Show | 168 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.2358+1777T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375597 | ||||||
| chr5:123375790
|
T | C | 2 | a0001c0005t0003g0082a0001c0005t0003g0084 | 2 | HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2358+1584A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375790 | ||||||
| chr5:123375947
|
T | C | 23 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(20): Show | 27 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.2358+1427A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375947 | ||||||
| chr5:123375993
|
C | CT | 38 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(35): Show | 43 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.2358+1380dupA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375993 | ||||||
| chr5:123376070
|
A | G | 2 | a0002c0002t0001g0032a0002c0002t0001g0111 | 2 | HG03017.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2358+1304T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376070 | ||||||
| chr5:123376075
|
C | G | 1 | a0007c0017t0002g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2358+1299G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376075 | ||||||
| chr5:123376076
|
C | T | 1 | a0010c0019t0003g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2358+1298G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376076 | ||||||
| chr5:123376095
|
C | A | 1 | a0005c0007t0003g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2358+1279G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376095 | ||||||
| chr5:123376147
|
C | T | 163 | a0001c0006t0001g0103a0001c0006t0002g0006a0001c0006t0002g0204others(160): Show | 183 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.2358+1227G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376147 | ||||||
| chr5:123376152
|
T | A | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2358+1222A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376152 | ||||||
| chr5:123376452
|
T | C | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2358+922A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376452 | ||||||
| chr5:123376462
|
T | C | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2358+912A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376462 | ||||||
| chr5:123376549
|
C | T | 1 | a0003c0003t0001g0303 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2358+825G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376549 | ||||||
| chr5:123376597
|
G | A | 1 | a0003c0003t0001g0314 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2358+777C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376597 | ||||||
| chr5:123376694
|
G | A | 1 | a0001c0001t0002g0277 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2358+680C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376694 | ||||||
| chr5:123376825
|
G | C | 199 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(196): Show | 223 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.2358+549C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376825 | ||||||
| chr5:123376869
|
G | A | 33 | a0001c0005t0003g0323a0004c0004t0003g0013a0004c0004t0003g0015others(30): Show | 35 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2358+505C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376869 | ||||||
| chr5:123376874
|
G | A | 2 | a0001c0006t0002g0204a0001c0006t0002g0205 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2358+500C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376874 | ||||||
| chr5:123376903
|
C | G | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2358+471G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376903 | ||||||
| chr5:123377019
|
G | T | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2358+355C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123377019 | ||||||
| chr5:123377354
|
T | C | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2358+20A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123377354 | ||||||
| chr5:123377360
|
G | A | 1 | a0001c0001t0002g0317 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2358+14C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123377360 | ||||||
| chr5:123377545
|
A | C | 1 | a0001c0005t0003g0091 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2197-10T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 15/19 | chr5 | 123377545 | ||||||
| chr5:123377951
|
C | T | 2 | a0002c0002t0001g0117a0002c0002t0001g0123 | 2 | HG00597.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.2196+385G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 15/19 | chr5 | 123377951 | ||||||
| chr5:123378145
|
TA | T | 150 | a0001c0006t0001g0103a0001c0006t0008g0010a0001c0006t0009g0030others(147): Show | 168 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.2196+190delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 15/19 | chr5 | 123378145 | ||||||
| chr5:123378243
|
G | A | 1 | a0007c0017t0002g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2196+93C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 15/19 | chr5 | 123378243 | ||||||
| chr5:123378295
|
C | T | 45 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(42): Show | 51 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.2196+41G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 15/19 | chr5 | 123378295 | ||||||
| chr5:123378440
|
T | TA | 15 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(12): Show | 17 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2104-13dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378440 | ||||||
| chr5:123378440
|
TA | T | 6 | a0001c0005t0003g0323a0002c0002t0001g0155a0004c0004t0003g0058others(3): Show | 6 | HG01891.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2104-13delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378440 | ||||||
| chr5:123378440
|
TAAAAAA | T | 38 | a0001c0006t0001g0103a0002c0002t0001g0005a0002c0002t0001g0016others(35): Show | 43 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.2104-18_2104-13del others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378440 | ||||||
| chr5:123378498
|
C | A | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2104-70G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378498 | ||||||
| chr5:123378528
|
G | C | 2 | a0002c0002t0001g0212a0002c0002t0001g0213 | 2 | HG02055.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.2104-100C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378528 | ||||||
| chr5:123378562
|
G | T | 1 | a0001c0013t0004g0242 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2104-134C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378562 | ||||||
| chr5:123378647
|
A | G | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2104-219T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378647 | ||||||
| chr5:123378772
|
T | A | 1 | a0003c0003t0001g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2104-344A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378772 | ||||||
| chr5:123378783
|
A | C | 110 | a0002c0002t0001g0019a0002c0002t0001g0095a0002c0002t0001g0116others(107): Show | 122 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.2104-355T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378783 | ||||||
| chr5:123378798
|
G | C | 2 | a0002c0002t0001g0200a0002c0002t0001g0201 | 2 | HG00323.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2104-370C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378798 | ||||||
| chr5:123379036
|
A | C | 5 | a0002c0002t0001g0095a0002c0002t0001g0198a0002c0002t0001g0199others(2): Show | 5 | HG00323.hp1 HG00642.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.2104-608T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379036 | ||||||
| chr5:123379044
|
A | T | 1 | a0004c0004t0003g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2104-616T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379044 | ||||||
| chr5:123379096
|
C | G | 1 | a0004c0004t0003g0039 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2104-668G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379096 | ||||||
| chr5:123379149
|
G | A | 39 | a0002c0002t0001g0019a0002c0002t0001g0095a0002c0002t0001g0116others(36): Show | 40 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.2104-721C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379149 | ||||||
| chr5:123379278
|
A | G | 199 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(196): Show | 223 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.2104-850T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379278 | ||||||
| chr5:123379300
|
C | T | 1 | a0002c0008t0002g0217 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2104-872G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379300 | ||||||
| chr5:123379377
|
T | A | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2104-949A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379377 | ||||||
| chr5:123379386
|
T | C | 1 | a0003c0003t0001g0296 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2104-958A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379386 | ||||||
| chr5:123379416
|
T | C | 3 | a0006c0010t0002g0202a0006c0010t0015g0033a0007c0017t0002g0209 | 3 | HG01243.hp1 HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2104-988A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379416 | ||||||
| chr5:123379420
|
A | C | 1 | a0005c0007t0003g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2104-992T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379420 | ||||||
| chr5:123379445
|
A | G | 15 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0002g0035others(12): Show | 17 | HG01496.hp2 HG02258.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.2104-1017T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379445 | ||||||
| chr5:123379542
|
A | G | 1 | a0001c0005t0005g0064 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2104-1114T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379542 | ||||||
| chr5:123379724
|
A | G | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2104-1296T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379724 | ||||||
| chr5:123379781
|
C | G | 1 | a0003c0003t0001g0300 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2104-1353G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379781 | ||||||
| chr5:123380212
|
CT | C | 7 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0216others(4): Show | 9 | NA18944.hp1 NA18946.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.2104-1785delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123380212 | ||||||
| chr5:123380228
|
C | T | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2104-1800G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123380228 | ||||||
| chr5:123380670
|
A | G | 2 | a0001c0001t0002g0225a0001c0001t0002g0241 | 2 | HG02074.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2103+1441T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123380670 | ||||||
| chr5:123381028
|
A | AAGTT | 32 | a0001c0005t0003g0323a0004c0004t0003g0013a0004c0004t0003g0015others(29): Show | 34 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.2103+1079_2103+108 others(8): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381028 | ||||||
| chr5:123381103
|
T | C | 36 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(33): Show | 40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2103+1008A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381103 | ||||||
| chr5:123381125
|
C | A | 229 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(226): Show | 255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.2103+986G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381125 | ||||||
| chr5:123381197
|
A | G | 13 | a0001c0005t0003g0082a0001c0005t0003g0083a0001c0005t0003g0084others(10): Show | 13 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2103+914T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381197 | ||||||
| chr5:123381221
|
A | C | 162 | a0001c0006t0001g0103a0001c0006t0002g0006a0001c0006t0002g0204others(159): Show | 182 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.2103+890T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381221 | ||||||
| chr5:123381377
|
A | AGGAGCAC others(1): Show |
162 | a0001c0006t0001g0103a0001c0006t0002g0006a0001c0006t0002g0204others(159): Show | 182 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.2103+726_2103+733d others(10): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381377 | ||||||
| chr5:123381607
|
T | C | 26 | a0004c0004t0003g0013a0004c0004t0003g0015a0004c0004t0003g0037others(23): Show | 28 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.2103+504A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381607 | ||||||
| chr5:123381742
|
T | C | 1 | a0001c0001t0002g0275 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2103+369A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381742 | ||||||
| chr5:123381758
|
C | T | 1 | a0001c0001t0002g0268 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2103+353G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381758 | ||||||
| chr5:123381766
|
T | C | 150 | a0001c0001t0002g0275a0001c0006t0001g0103a0001c0006t0008g0010others(147): Show | 168 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.2103+345A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381766 | ||||||
| chr5:123381767
|
AT | A | 151 | a0001c0001t0002g0275a0001c0006t0001g0103a0001c0006t0008g0010others(148): Show | 169 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.2103+343delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381767 | ||||||
| chr5:123381820
|
T | A | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2103+291A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381820 | ||||||
| chr5:123381969
|
C | G | 1 | a0001c0005t0003g0091 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2103+142G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381969 | ||||||
| chr5:123382046
|
C | T | 5 | a0002c0002t0001g0113a0002c0002t0001g0212a0002c0002t0001g0213others(2): Show | 5 | HG00438.hp1 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2103+65G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123382046 | ||||||
| chr5:123382226
|
G | T | 2 | a0001c0001t0002g0279a0001c0001t0002g0280 | 2 | HG01123.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2014-26C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382226 | ||||||
| chr5:123382263
|
T | C | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2014-63A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382263 | ||||||
| chr5:123382324
|
C | A | 16 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0002g0035others(13): Show | 18 | HG01496.hp2 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.2014-124G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382324 | ||||||
| chr5:123382325
|
T | TA | 26 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(23): Show | 30 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.2014-126dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382325 | ||||||
| chr5:123382325
|
TA | T | 46 | a0001c0001t0002g0240a0001c0001t0002g0315a0001c0001t0004g0232others(43): Show | 51 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.2014-126delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382325 | ||||||
| chr5:123382326
|
A | T | 1 | a0001c0001t0002g0034 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2014-126T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382326 | ||||||
| chr5:123382350
|
G | T | 149 | a0001c0006t0001g0103a0001c0006t0008g0010a0001c0006t0009g0030others(146): Show | 167 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.2014-150C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382350 | ||||||
| chr5:123382354
|
C | A | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2014-154G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382354 | ||||||
| chr5:123382442
|
A | G | 32 | a0001c0005t0003g0323a0004c0004t0003g0013a0004c0004t0003g0015others(29): Show | 34 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.2014-242T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382442 | ||||||
| chr5:123382545
|
G | A | 4 | a0004c0004t0003g0049a0004c0004t0003g0050a0004c0004t0003g0056others(1): Show | 4 | NA18982.hp1 NA18990.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.2013+192C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382545 | ||||||
| chr5:123382647
|
C | T | 36 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(33): Show | 40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2013+90G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382647 | ||||||
| chr5:123382654
|
T | C | 4 | a0002c0008t0002g0217a0002c0008t0002g0218a0002c0008t0002g0219others(1): Show | 4 | NA18949.hp2 NA18950.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.2013+83A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382654 | ||||||
| chr5:123382934
|
T | C | 1 | a0001c0005t0003g0323 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1861-45A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 12/19 | chr5 | 123382934 | ||||||
| chr5:123383200
|
A | G | 1 | a0001c0001t0002g0279 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1764-118T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123383200 | ||||||
| chr5:123383502
|
T | C | 1 | a0003c0003t0001g0302 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1764-420A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123383502 | ||||||
| chr5:123383612
|
T | C | 1 | a0001c0001t0002g0222 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1764-530A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123383612 | ||||||
| chr5:123383633
|
T | C | 1 | a0004c0004t0003g0053 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1764-551A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123383633 | ||||||
| chr5:123383848
|
C | A | 2 | a0001c0006t0002g0204a0001c0006t0002g0205 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1764-766G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123383848 | ||||||
| chr5:123383988
|
T | A | 149 | a0001c0006t0001g0103a0001c0006t0008g0010a0001c0006t0009g0030others(146): Show | 167 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.1764-906A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123383988 | ||||||
| chr5:123384253
|
T | C | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1763+698A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384253 | ||||||
| chr5:123384287
|
CTTGT | C | 145 | a0001c0006t0001g0103a0002c0002t0001g0005a0002c0002t0001g0016others(142): Show | 161 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1763+660_1763+663d others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384287 | ||||||
| chr5:123384290
|
G | C | 2 | a0002c0002t0001g0017a0002c0002t0001g0105 | 3 | HG00735.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1763+661C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384290 | ||||||
| chr5:123384292
|
T | C | 2 | a0002c0002t0001g0017a0002c0002t0001g0105 | 3 | HG00735.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1763+659A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384292 | ||||||
| chr5:123384293
|
TCTC | T | 2 | a0002c0002t0001g0017a0002c0002t0001g0105 | 3 | HG00735.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1763+655_1763+657d others(5): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384293 | ||||||
| chr5:123384326
|
G | A | 147 | a0001c0006t0001g0103a0002c0002t0001g0005a0002c0002t0001g0016others(144): Show | 164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1763+625C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384326 | ||||||
| chr5:123384423
|
A | T | 1 | a0001c0001t0002g0237 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1763+528T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384423 | ||||||
| chr5:123384431
|
G | A | 1 | a0007c0017t0002g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1763+520C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384431 | ||||||
| chr5:123384613
|
A | G | 4 | a0002c0002t0001g0095a0002c0002t0001g0198a0002c0002t0001g0200others(1): Show | 4 | HG00323.hp1 HG00642.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1763+338T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384613 | ||||||
| chr5:123384639
|
A | C | 1 | a0001c0001t0002g0287 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1763+312T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384639 | ||||||
| chr5:123385229
|
T | A | 149 | a0001c0006t0001g0103a0001c0006t0008g0010a0001c0006t0009g0030others(146): Show | 167 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.1581-96A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123385229 | ||||||
| chr5:123385252
|
G | A | 1 | a0002c0002t0001g0126 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1581-119C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123385252 | ||||||
| chr5:123385394
|
C | T | 68 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(65): Show | 74 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.1581-261G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123385394 | ||||||
| chr5:123385559
|
G | T | 69 | a0001c0001t0002g0321a0001c0005t0003g0011a0001c0005t0003g0063others(66): Show | 75 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.1581-426C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123385559 | ||||||
| chr5:123385619
|
GT | G | 159 | a0001c0006t0001g0103a0001c0006t0002g0006a0001c0006t0002g0205others(156): Show | 179 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1581-487delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123385619 | ||||||
| chr5:123385692
|
C | T | 162 | a0001c0006t0001g0103a0001c0006t0002g0006a0001c0006t0002g0204others(159): Show | 182 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.1581-559G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123385692 | ||||||
| chr5:123385862
|
C | T | 2 | a0001c0005t0003g0011a0001c0005t0003g0081 | 3 | HG01255.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1580+656G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123385862 | ||||||
| chr5:123385984
|
G | A | 2 | a0002c0002t0001g0032a0002c0002t0001g0111 | 2 | HG03017.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1580+534C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123385984 | ||||||
| chr5:123386042
|
G | T | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1580+476C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123386042 | ||||||
| chr5:123386111
|
G | A | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1580+407C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123386111 | ||||||
| chr5:123386124
|
A | C | 3 | a0002c0002t0001g0211a0002c0002t0001g0212a0002c0002t0001g0213 | 3 | HG02055.hp2 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1580+394T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123386124 | ||||||
| chr5:123386158
|
A | C | 10 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1580+360T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123386158 | ||||||
| chr5:123386179
|
T | C | 1 | a0001c0005t0005g0064 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1580+339A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123386179 | ||||||
| chr5:123386200
|
T | G | 2 | a0003c0003t0001g0022a0003c0003t0001g0195 | 3 | NA18959.hp1 NA18974.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1580+318A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123386200 | ||||||
| chr5:123386306
|
G | A | 1 | a0004c0004t0003g0013 | 2 | HG01167.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1580+212C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123386306 | ||||||
| chr5:123386673
|
AT | A | 53 | a0001c0006t0001g0103a0001c0006t0002g0006a0001c0006t0002g0207others(50): Show | 61 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(58): Show |
splice_region_variant&intron_variant | LOW | c.1431-7delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386673 | ||||||
| chr5:123386674
|
T | A | 6 | a0001c0006t0002g0204a0001c0006t0002g0205a0001c0006t0002g0206others(3): Show | 6 | HG02257.hp1 HG02970.hp1 HG03041.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1431-7A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386674 | ||||||
| chr5:123386675
|
T | A | 4 | a0001c0006t0002g0006a0001c0006t0002g0207a0001c0006t0013g0208others(1): Show | 6 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1431-8A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386675 | ||||||
| chr5:123386675
|
T | TA | 4 | a0002c0002t0001g0151a0002c0002t0001g0157a0002c0002t0001g0162others(1): Show | 4 | HG03579.hp2 NA18939.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1431-9_1431-8insT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386675 | ||||||
| chr5:123386675
|
TTA | T | 3 | a0001c0006t0003g0322a0002c0002t0001g0104a0007c0017t0002g0209 | 3 | HG01070.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1431-10_1431-9delT others(1): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386675 | ||||||
| chr5:123386676
|
T | A | 105 | a0001c0006t0002g0204a0001c0006t0002g0205a0001c0006t0002g0206others(102): Show | 117 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.1431-9A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386676 | ||||||
| chr5:123386676
|
T | TA | 10 | a0001c0005t0003g0323a0001c0005t0005g0064a0001c0005t0005g0072others(7): Show | 10 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1431-10dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386676 | ||||||
| chr5:123386676
|
T | TAA | 54 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(51): Show | 60 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.1431-11_1431-10dup others(2): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386676 | ||||||
| chr5:123386678
|
A | T | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1431-11T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386678 | ||||||
| chr5:123386874
|
C | T | 147 | a0001c0006t0001g0103a0002c0002t0001g0005a0002c0002t0001g0016others(144): Show | 164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1431-207G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386874 | ||||||
| chr5:123386900
|
T | C | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1431-233A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386900 | ||||||
| chr5:123387243
|
C | G | 2 | a0004c0004t0003g0058a0004c0004t0003g0059 | 2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1431-576G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123387243 | ||||||
| chr5:123387464
|
G | C | 1 | a0001c0006t0009g0030 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1431-797C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123387464 | ||||||
| chr5:123387570
|
G | T | 149 | a0001c0006t0001g0103a0001c0006t0008g0010a0001c0006t0009g0030others(146): Show | 167 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.1430+862C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123387570 | ||||||
| chr5:123387784
|
C | T | 1 | a0003c0003t0001g0299 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1430+648G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123387784 | ||||||
| chr5:123387788
|
C | G | 2 | a0002c0002t0001g0112a0002c0002t0014g0124 | 2 | HG01081.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1430+644G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123387788 | ||||||
| chr5:123387899
|
C | T | 162 | a0001c0006t0001g0103a0001c0006t0002g0006a0001c0006t0002g0204others(159): Show | 182 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.1430+533G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123387899 | ||||||
| chr5:123387992
|
A | G | 1 | a0001c0005t0005g0080 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1430+440T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123387992 | ||||||
| chr5:123388013
|
CTTTTTGA others(49): Show |
C | 162 | a0001c0006t0001g0103a0001c0006t0002g0006a0001c0006t0002g0204others(159): Show | 182 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.1430+363_1430+418d others(58): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123388013 | ||||||
| chr5:123388258
|
T | C | 1 | a0001c0005t0003g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1430+174A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123388258 | ||||||
| chr5:123388316
|
C | T | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1430+116G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123388316 | ||||||
| chr5:123388730
|
T | C | 8 | a0002c0002t0001g0143a0002c0002t0001g0144a0002c0002t0001g0157others(5): Show | 8 | NA18939.hp2 NA18960.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.1256-124A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123388730 | ||||||
| chr5:123388752
|
A | G | 70 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0005t0003g0011others(67): Show | 76 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.1256-146T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123388752 | ||||||
| chr5:123388804
|
T | C | 3 | a0002c0002t0001g0211a0002c0002t0001g0212a0002c0002t0001g0213 | 3 | HG02055.hp2 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1256-198A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123388804 | ||||||
| chr5:123388850
|
G | A | 4 | a0002c0002t0001g0005a0002c0002t0001g0130a0002c0002t0001g0131others(1): Show | 6 | HG02027.hp1 NA18950.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.1256-244C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123388850 | ||||||
| chr5:123388944
|
A | T | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1256-338T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123388944 | ||||||
| chr5:123388973
|
C | A | 148 | a0001c0006t0008g0010a0001c0006t0009g0030a0002c0002t0001g0005others(145): Show | 166 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.1256-367G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123388973 | ||||||
| chr5:123389258
|
G | A | 1 | a0001c0001t0002g0277 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1256-652C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389258 | ||||||
| chr5:123389291
|
CAACTGTT others(7): Show |
C | 2 | a0003c0003t0001g0183a0003c0003t0001g0193 | 2 | HG02145.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1255+619_1255+632d others(16): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389291 | ||||||
| chr5:123389358
|
T | C | 1 | a0002c0002t0001g0170 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1255+566A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389358 | ||||||
| chr5:123389394
|
G | C | 4 | a0002c0008t0002g0217a0002c0008t0002g0218a0002c0008t0002g0219others(1): Show | 4 | NA18949.hp2 NA18950.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255+530C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389394 | ||||||
| chr5:123389536
|
T | C | 4 | a0001c0001t0004g0009a0001c0001t0004g0238a0001c0001t0004g0253others(1): Show | 6 | HG01433.hp2 HG01952.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1255+388A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389536 | ||||||
| chr5:123389562
|
G | A | 2 | a0004c0004t0003g0043a0004c0004t0003g0044 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1255+362C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389562 | ||||||
| chr5:123389563
|
C | T | 148 | a0001c0006t0008g0010a0001c0006t0009g0030a0002c0002t0001g0005others(145): Show | 166 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.1255+361G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389563 | ||||||
| chr5:123389741
|
C | G | 70 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0005t0003g0011others(67): Show | 76 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.1255+183G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389741 | ||||||
| chr5:123389751
|
C | T | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1255+173G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389751 | ||||||
| chr5:123389803
|
T | C | 34 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0005t0003g0323others(31): Show | 36 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1255+121A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389803 | ||||||
| chr5:123389884
|
A | G | 1 | a0003c0003t0001g0183 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1255+40T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389884 | ||||||
| chr5:123390159
|
T | C | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1039-19A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 7/19 | chr5 | 123390159 | ||||||
| chr5:123390520
|
C | T | 1 | a0001c0005t0003g0323 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1039-380G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 7/19 | chr5 | 123390520 | ||||||
| chr5:123390700
|
C | T | 1 | a0002c0002t0001g0032 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1038+410G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 7/19 | chr5 | 123390700 | ||||||
| chr5:123390856
|
G | A | 2 | a0001c0006t0008g0010a0001c0006t0009g0030 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1038+254C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 7/19 | chr5 | 123390856 | ||||||
| chr5:123390877
|
T | C | 1 | a0003c0003t0001g0137 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1038+233A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 7/19 | chr5 | 123390877 | ||||||
| chr5:123390973
|
G | A | 1 | a0002c0002t0001g0138 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1038+137C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 7/19 | chr5 | 123390973 | ||||||
| chr5:123391089
|
T | C | 36 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(33): Show | 40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1038+21A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 7/19 | chr5 | 123391089 | ||||||
| chr5:123391381
|
C | T | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.811-44G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123391381 | ||||||
| chr5:123391444
|
T | A | 324 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0014others(321): Show | 372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.811-107A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123391444 | ||||||
| chr5:123391477
|
G | T | 230 | a0001c0001t0002g0321a0001c0005t0003g0011a0001c0005t0003g0063others(227): Show | 256 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.811-140C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123391477 | ||||||
| chr5:123391501
|
C | G | 2 | a0002c0002t0001g0117a0002c0002t0001g0123 | 2 | HG00597.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.811-164G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123391501 | ||||||
| chr5:123391536
|
A | T | 4 | a0001c0006t0002g0006a0001c0006t0002g0207a0001c0006t0013g0208others(1): Show | 6 | HG01069.hp1 HG01071.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.811-199T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123391536 | ||||||
| chr5:123391602
|
CTTCTTT | C | 149 | a0001c0006t0008g0010a0001c0006t0009g0030a0002c0002t0001g0005others(146): Show | 167 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.811-271_811-266del others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123391602 | ||||||
| chr5:123391904
|
G | A | 232 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0321others(229): Show | 258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.811-567C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123391904 | ||||||
| chr5:123392066
|
T | C | 1 | a0003c0003t0001g0297 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.811-729A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392066 | ||||||
| chr5:123392125
|
T | C | 164 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(161): Show | 185 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.811-788A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392125 | ||||||
| chr5:123392208
|
T | C | 1 | a0001c0001t0002g0280 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.811-871A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392208 | ||||||
| chr5:123392234
|
G | A | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.811-897C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392234 | ||||||
| chr5:123392267
|
C | T | 232 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0321others(229): Show | 258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.811-930G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392267 | ||||||
| chr5:123392431
|
C | T | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.810+869G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392431 | ||||||
| chr5:123392567
|
C | G | 231 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0005t0003g0011others(228): Show | 257 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.810+733G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392567 | ||||||
| chr5:123392654
|
G | A | 2 | a0002c0002t0001g0166a0002c0002t0001g0170 | 2 | NA19006.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.810+646C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392654 | ||||||
| chr5:123392715
|
G | A | 1 | a0001c0001t0007g0326 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.810+585C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392715 | ||||||
| chr5:123392718
|
C | T | 1 | a0004c0004t0003g0051 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.810+582G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392718 | ||||||
| chr5:123392747
|
T | G | 2 | a0002c0002t0001g0174a0002c0002t0001g0175 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.810+553A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392747 | ||||||
| chr5:123392911
|
G | A | 1 | a0009c0014t0005g0076 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.810+389C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392911 | ||||||
| chr5:123393219
|
C | T | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.810+81G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123393219 | ||||||
| chr5:123393531
|
C | T | 5 | a0002c0002t0001g0156a0002c0002t0001g0158a0002c0002t0001g0159others(2): Show | 5 | NA18944.hp2 NA18948.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.613-34G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123393531 | ||||||
| chr5:123393536
|
T | A | 70 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0005t0003g0011others(67): Show | 76 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.613-39A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123393536 | ||||||
| chr5:123393615
|
C | T | 2 | a0003c0003t0001g0182a0003c0003t0001g0187 | 2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.613-118G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123393615 | ||||||
| chr5:123393675
|
AAGAGTCG others(4): Show |
A | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.613-189_613-179del others(11): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123393675 | ||||||
| chr5:123393682
|
G | A | 230 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0005t0003g0011others(227): Show | 256 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.613-185C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123393682 | ||||||
| chr5:123393701
|
T | C | 1 | a0002c0002t0001g0109 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.613-204A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123393701 | ||||||
| chr5:123393735
|
T | C | 1 | a0002c0002t0018g0328 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.613-238A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123393735 | ||||||
| chr5:123393985
|
G | T | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.613-488C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123393985 | ||||||
| chr5:123394014
|
T | G | 13 | a0001c0005t0003g0082a0001c0005t0003g0083a0001c0005t0003g0084others(10): Show | 13 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.613-517A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394014 | ||||||
| chr5:123394245
|
T | C | 1 | a0007c0017t0002g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.613-748A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394245 | ||||||
| chr5:123394304
|
C | T | 232 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0321others(229): Show | 258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.613-807G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394304 | ||||||
| chr5:123394348
|
A | G | 10 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.613-851T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394348 | ||||||
| chr5:123394394
|
C | T | 2 | a0004c0004t0003g0043a0004c0004t0003g0044 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.613-897G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394394 | ||||||
| chr5:123394602
|
C | T | 1 | a0002c0002t0001g0122 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.613-1105G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394602 | ||||||
| chr5:123394616
|
A | G | 1 | a0002c0002t0001g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.613-1119T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394616 | ||||||
| chr5:123394669
|
A | G | 10 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.613-1172T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394669 | ||||||
| chr5:123394875
|
T | C | 1 | a0003c0003t0001g0299 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.613-1378A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394875 | ||||||
| chr5:123394917
|
C | A | 3 | a0003c0003t0001g0186a0003c0003t0001g0188a0003c0003t0001g0190 | 3 | HG02698.hp2 HG02738.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.613-1420G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394917 | ||||||
| chr5:123394935
|
G | A | 40 | a0002c0002t0001g0005a0002c0002t0001g0016a0002c0002t0001g0017others(37): Show | 45 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.613-1438C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394935 | ||||||
| chr5:123394957
|
G | T | 148 | a0001c0006t0008g0010a0001c0006t0009g0030a0002c0002t0001g0005others(145): Show | 166 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.613-1460C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394957 | ||||||
| chr5:123394959
|
C | G | 17 | a0001c0005t0005g0004a0001c0005t0005g0012a0001c0005t0005g0036others(14): Show | 20 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.613-1462G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394959 | ||||||
| chr5:123395163
|
G | A | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.613-1666C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395163 | ||||||
| chr5:123395190
|
C | A | 6 | a0001c0006t0002g0006a0001c0006t0002g0206a0001c0006t0002g0207others(3): Show | 8 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.613-1693G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395190 | ||||||
| chr5:123395228
|
C | T | 231 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0321others(228): Show | 257 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.613-1731G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395228 | ||||||
| chr5:123395290
|
G | A | 1 | a0001c0001t0002g0222 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.613-1793C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395290 | ||||||
| chr5:123395292
|
C | G | 1 | a0001c0001t0002g0267 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.613-1795G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395292 | ||||||
| chr5:123395311
|
A | G | 11 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(8): Show | 13 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.613-1814T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395311 | ||||||
| chr5:123395470
|
C | G | 11 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(8): Show | 13 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.613-1973G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395470 | ||||||
| chr5:123395508
|
C | G | 1 | a0002c0002t0001g0157 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.613-2011G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395508 | ||||||
| chr5:123395534
|
C | T | 1 | a0001c0006t0002g0324 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.613-2037G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395534 | ||||||
| chr5:123395585
|
G | A | 1 | a0005c0007t0003g0086 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.613-2088C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395585 | ||||||
| chr5:123395681
|
C | CT | 12 | a0001c0001t0002g0264a0004c0004t0003g0013a0004c0004t0003g0037others(9): Show | 13 | HG01167.hp2 HG01192.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.613-2185dupA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395681 | ||||||
| chr5:123395681
|
CT | C | 15 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(12): Show | 17 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.613-2185delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395681 | ||||||
| chr5:123395681
|
CTT | C | 143 | a0001c0006t0003g0322a0001c0006t0008g0010a0001c0016t0002g0210others(140): Show | 161 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.613-2186_613-2185d others(4): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395681 | ||||||
| chr5:123395702
|
G | T | 1 | a0001c0001t0004g0238 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.613-2205C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395702 | ||||||
| chr5:123395708
|
T | A | 11 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(8): Show | 13 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.613-2211A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395708 | ||||||
| chr5:123395708
|
T | G | 150 | a0001c0006t0003g0322a0001c0006t0008g0010a0001c0006t0009g0030others(147): Show | 168 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.613-2211A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395708 | ||||||
| chr5:123395712
|
T | C | 231 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0005t0003g0011others(228): Show | 257 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.613-2215A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395712 | ||||||
| chr5:123395753
|
C | T | 1 | a0003c0003t0001g0319 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.613-2256G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395753 | ||||||
| chr5:123395872
|
T | A | 1 | a0001c0011t0002g0203 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.613-2375A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395872 | ||||||
| chr5:123395874
|
G | C | 148 | a0001c0006t0008g0010a0001c0006t0009g0030a0002c0002t0001g0005others(145): Show | 166 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.613-2377C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395874 | ||||||
| chr5:123395924
|
C | T | 3 | a0001c0001t0002g0258a0004c0004t0003g0058a0004c0004t0003g0059 | 3 | HG02809.hp1 HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.613-2427G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395924 | ||||||
| chr5:123395989
|
C | CT | 35 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0237others(32): Show | 36 | HG00609.hp2 HG01070.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.613-2493dupA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395989 | ||||||
| chr5:123395989
|
CT | C | 111 | a0001c0001t0002g0263a0001c0005t0005g0071a0001c0006t0002g0006others(108): Show | 125 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.613-2493delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395989 | ||||||
| chr5:123396020
|
G | A | 1 | a0003c0003t0001g0139 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.613-2523C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396020 | ||||||
| chr5:123396120
|
A | C | 1 | a0001c0006t0009g0030 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.613-2623T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396120 | ||||||
| chr5:123396196
|
C | T | 34 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0005t0003g0323others(31): Show | 36 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.613-2699G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396196 | ||||||
| chr5:123396202
|
T | C | 1 | a0001c0006t0008g0010 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.613-2705A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396202 | ||||||
| chr5:123396217
|
T | C | 1 | a0001c0001t0002g0228 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.613-2720A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396217 | ||||||
| chr5:123396227
|
C | CT | 2 | a0001c0005t0005g0012a0001c0005t0005g0073 | 3 | HG01496.hp1 HG01943.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.613-2731dupA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396227 | ||||||
| chr5:123396342
|
T | G | 1 | a0001c0005t0003g0323 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.612+2794A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396342 | ||||||
| chr5:123396355
|
C | T | 5 | a0001c0006t0002g0006a0001c0006t0002g0206a0001c0006t0002g0207others(2): Show | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.612+2781G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396355 | ||||||
| chr5:123396356
|
T | G | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.612+2780A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396356 | ||||||
| chr5:123396409
|
C | A | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.612+2727G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396409 | ||||||
| chr5:123396416
|
C | A | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.612+2720G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396416 | ||||||
| chr5:123396435
|
T | C | 2 | a0004c0004t0003g0041a0004c0004t0003g0042 | 2 | NA18968.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.612+2701A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396435 | ||||||
| chr5:123396472
|
T | G | 2 | a0001c0006t0002g0204a0001c0006t0002g0205 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.612+2664A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396472 | ||||||
| chr5:123396542
|
T | C | 232 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0321others(229): Show | 258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.612+2594A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396542 | ||||||
| chr5:123396587
|
T | C | 1 | a0003c0003t0001g0298 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.612+2549A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396587 | ||||||
| chr5:123396648
|
G | A | 7 | a0004c0004t0003g0015a0004c0004t0003g0043a0004c0004t0003g0044others(4): Show | 8 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.612+2488C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396648 | ||||||
| chr5:123396879
|
A | C | 2 | a0002c0002t0001g0174a0002c0002t0001g0175 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.612+2257T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396879 | ||||||
| chr5:123397012
|
T | C | 13 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(10): Show | 15 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.612+2124A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123397012 | ||||||
| chr5:123397325
|
A | C | 11 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(8): Show | 13 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.612+1811T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123397325 | ||||||
| chr5:123397379
|
A | G | 1 | a0003c0003t0001g0193 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.612+1757T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123397379 | ||||||
| chr5:123397623
|
G | A | 146 | a0002c0002t0001g0005a0002c0002t0001g0016a0002c0002t0001g0017others(143): Show | 163 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.612+1513C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123397623 | ||||||
| chr5:123397701
|
G | C | 148 | a0001c0006t0008g0010a0001c0006t0009g0030a0002c0002t0001g0005others(145): Show | 166 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.612+1435C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123397701 | ||||||
| chr5:123397789
|
A | C | 1 | a0004c0004t0003g0052 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.612+1347T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123397789 | ||||||
| chr5:123397839
|
C | T | 2 | a0001c0006t0008g0010a0001c0006t0009g0030 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.612+1297G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123397839 | ||||||
| chr5:123397862
|
T | C | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.612+1274A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123397862 | ||||||
| chr5:123398009
|
T | C | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.612+1127A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398009 | ||||||
| chr5:123398187
|
A | G | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.612+949T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398187 | ||||||
| chr5:123398311
|
G | T | 148 | a0001c0006t0008g0010a0001c0006t0009g0030a0002c0002t0001g0005others(145): Show | 166 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.612+825C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398311 | ||||||
| chr5:123398364
|
G | T | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.612+772C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398364 | ||||||
| chr5:123398393
|
T | C | 1 | a0001c0001t0004g0226 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.612+743A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398393 | ||||||
| chr5:123398514
|
T | A | 1 | a0001c0001t0002g0263 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.612+622A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398514 | ||||||
| chr5:123398598
|
C | G | 1 | a0001c0005t0005g0073 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.612+538G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398598 | ||||||
| chr5:123398621
|
T | G | 1 | a0004c0004t0003g0045 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.612+515A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398621 | ||||||
| chr5:123398824
|
C | G | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.612+312G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398824 | ||||||
| chr5:123398967
|
T | C | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.612+169A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398967 | ||||||
| chr5:123399030
|
T | TA | 160 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(157): Show | 180 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.612+105dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123399030 | ||||||
| chr5:123399758
|
A | T | 36 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(33): Show | 40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.464-474T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123399758 | ||||||
| chr5:123399812
|
C | T | 2 | a0001c0001t0002g0235a0001c0001t0002g0236 | 2 | HG02735.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.464-528G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123399812 | ||||||
| chr5:123399980
|
T | C | 1 | a0001c0001t0002g0259 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.464-696A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123399980 | ||||||
| chr5:123400048
|
G | A | 2 | a0001c0006t0008g0010a0001c0006t0009g0030 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.464-764C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400048 | ||||||
| chr5:123400056
|
A | T | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-772T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400056 | ||||||
| chr5:123400172
|
G | A | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.464-888C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400172 | ||||||
| chr5:123400263
|
A | G | 1 | a0004c0004t0003g0047 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.464-979T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400263 | ||||||
| chr5:123400274
|
T | C | 2 | a0001c0006t0008g0010a0001c0006t0009g0030 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.464-990A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400274 | ||||||
| chr5:123400275
|
C | A | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.464-991G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400275 | ||||||
| chr5:123400275
|
C | T | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.464-991G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400275 | ||||||
| chr5:123400402
|
G | A | 2 | a0001c0001t0002g0254a0001c0001t0002g0281 | 2 | HG00140.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.464-1118C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400402 | ||||||
| chr5:123400450
|
T | C | 1 | a0002c0002t0001g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.464-1166A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400450 | ||||||
| chr5:123400595
|
A | G | 10 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.464-1311T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400595 | ||||||
| chr5:123400659
|
C | CT | 189 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0026others(186): Show | 210 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.464-1376dupA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400659 | ||||||
| chr5:123400659
|
C | CTT | 6 | a0002c0002t0018g0328a0003c0003t0001g0021a0003c0003t0001g0135others(3): Show | 7 | HG02027.hp2 HG02145.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.464-1377_464-1376d others(4): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400659 | ||||||
| chr5:123400704
|
C | CA | 38 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0287others(35): Show | 40 | HG00609.hp2 HG00621.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.464-1421dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400704 | ||||||
| chr5:123400704
|
CA | C | 163 | a0001c0001t0002g0264a0001c0001t0004g0025a0001c0001t0004g0232others(160): Show | 184 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.464-1421delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400704 | ||||||
| chr5:123400708
|
A | G | 1 | a0007c0017t0002g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.464-1424T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400708 | ||||||
| chr5:123400885
|
G | C | 149 | a0001c0006t0008g0010a0001c0006t0009g0030a0002c0002t0001g0005others(146): Show | 167 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.464-1601C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400885 | ||||||
| chr5:123400941
|
G | A | 13 | a0001c0005t0003g0082a0001c0005t0003g0083a0001c0005t0003g0084others(10): Show | 13 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.464-1657C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400941 | ||||||
| chr5:123400966
|
G | A | 12 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(9): Show | 14 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.464-1682C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400966 | ||||||
| chr5:123400973
|
G | A | 149 | a0001c0006t0008g0010a0001c0006t0009g0030a0002c0002t0001g0005others(146): Show | 167 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.464-1689C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400973 | ||||||
| chr5:123400974
|
A | ATCT | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-1693_464-1691d others(5): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400974 | ||||||
| chr5:123400998
|
T | G | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-1714A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400998 | ||||||
| chr5:123401088
|
T | C | 1 | a0001c0006t0009g0030 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.464-1804A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401088 | ||||||
| chr5:123401133
|
G | A | 1 | a0003c0003t0001g0101 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.464-1849C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401133 | ||||||
| chr5:123401154
|
C | T | 4 | a0002c0008t0002g0217a0002c0008t0002g0218a0002c0008t0002g0219others(1): Show | 4 | NA18949.hp2 NA18950.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-1870G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401154 | ||||||
| chr5:123401206
|
C | T | 9 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(6): Show | 11 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.464-1922G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401206 | ||||||
| chr5:123401208
|
T | C | 1 | a0002c0002t0001g0144 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.464-1924A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401208 | ||||||
| chr5:123401229
|
C | T | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.464-1945G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401229 | ||||||
| chr5:123401230
|
G | A | 1 | a0003c0003t0001g0179 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.464-1946C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401230 | ||||||
| chr5:123401234
|
C | T | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.464-1950G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401234 | ||||||
| chr5:123401259
|
C | T | 1 | a0003c0003t0001g0291 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.464-1975G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401259 | ||||||
| chr5:123401278
|
G | A | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-1994C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401278 | ||||||
| chr5:123401359
|
C | T | 2 | a0002c0002t0001g0110a0010c0019t0003g0108 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.464-2075G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401359 | ||||||
| chr5:123401455
|
A | G | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-2171T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401455 | ||||||
| chr5:123401475
|
G | A | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.464-2191C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401475 | ||||||
| chr5:123401476
|
C | A | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.464-2192G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401476 | ||||||
| chr5:123401514
|
C | T | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-2230G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401514 | ||||||
| chr5:123401563
|
G | A | 36 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(33): Show | 40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.464-2279C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401563 | ||||||
| chr5:123401705
|
C | T | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.464-2421G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401705 | ||||||
| chr5:123401728
|
A | C | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-2444T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401728 | ||||||
| chr5:123401745
|
CA | C | 233 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0321others(230): Show | 259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.464-2462delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401745 | ||||||
| chr5:123401804
|
C | T | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-2520G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401804 | ||||||
| chr5:123401898
|
C | T | 1 | a0001c0001t0002g0231 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.464-2614G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401898 | ||||||
| chr5:123401916
|
T | C | 2 | a0003c0003t0001g0188a0003c0003t0001g0190 | 2 | HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.464-2632A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401916 | ||||||
| chr5:123402007
|
C | T | 2 | a0001c0006t0008g0010a0001c0006t0009g0030 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.464-2723G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402007 | ||||||
| chr5:123402016
|
G | T | 2 | a0001c0006t0008g0010a0001c0006t0009g0030 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.464-2732C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402016 | ||||||
| chr5:123402097
|
C | T | 3 | a0003c0003t0001g0180a0003c0003t0001g0181a0006c0010t0015g0033 | 3 | HG01243.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.464-2813G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402097 | ||||||
| chr5:123402149
|
C | T | 35 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0005t0003g0323others(32): Show | 37 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.464-2865G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402149 | ||||||
| chr5:123402183
|
C | T | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-2899G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402183 | ||||||
| chr5:123402330
|
C | A | 233 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0321others(230): Show | 259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.464-3046G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402330 | ||||||
| chr5:123402367
|
C | A | 37 | a0002c0002t0001g0005a0002c0002t0001g0016a0002c0002t0001g0017others(34): Show | 42 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.464-3083G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402367 | ||||||
| chr5:123402382
|
A | G | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-3098T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402382 | ||||||
| chr5:123402502
|
C | A | 1 | a0004c0004t0003g0053 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.464-3218G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402502 | ||||||
| chr5:123402507
|
A | C | 23 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(20): Show | 27 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.464-3223T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402507 | ||||||
| chr5:123402522
|
C | T | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.464-3238G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402522 | ||||||
| chr5:123402529
|
C | T | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.464-3245G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402529 | ||||||
| chr5:123402585
|
C | G | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-3301G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402585 | ||||||
| chr5:123402628
|
G | A | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-3344C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402628 | ||||||
| chr5:123402886
|
T | C | 11 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(8): Show | 13 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.464-3602A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402886 | ||||||
| chr5:123402988
|
T | C | 233 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0321others(230): Show | 259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.464-3704A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402988 | ||||||
| chr5:123403446
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-4162C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123403446 | ||||||
| chr5:123403516
|
T | G | 13 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(10): Show | 15 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.464-4232A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123403516 | ||||||
| chr5:123403522
|
G | T | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.464-4238C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123403522 | ||||||
| chr5:123403548
|
T | C | 34 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0005t0003g0323others(31): Show | 36 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.464-4264A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123403548 | ||||||
| chr5:123403650
|
C | G | 1 | a0003c0003t0001g0292 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.464-4366G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123403650 | ||||||
| chr5:123403727
|
G | C | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-4443C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123403727 | ||||||
| chr5:123403809
|
C | T | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.464-4525G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123403809 | ||||||
| chr5:123403816
|
G | A | 8 | a0002c0008t0002g0217a0002c0008t0002g0218a0002c0008t0002g0219others(5): Show | 10 | NA18949.hp2 NA18950.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.464-4532C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123403816 | ||||||
| chr5:123404041
|
A | G | 146 | a0002c0002t0001g0005a0002c0002t0001g0016a0002c0002t0001g0017others(143): Show | 163 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.464-4757T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404041 | ||||||
| chr5:123404042
|
A | T | 1 | a0002c0002t0001g0126 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.464-4758T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404042 | ||||||
| chr5:123404060
|
G | A | 1 | a0002c0002t0001g0106 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.464-4776C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404060 | ||||||
| chr5:123404112
|
G | C | 1 | a0001c0001t0002g0223 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.464-4828C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404112 | ||||||
| chr5:123404138
|
A | C | 2 | a0001c0006t0008g0010a0001c0006t0009g0030 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.464-4854T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404138 | ||||||
| chr5:123404138
|
A | T | 2 | a0001c0006t0002g0204a0001c0006t0002g0205 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.464-4854T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404138 | ||||||
| chr5:123404165
|
T | TCATAA | 160 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(157): Show | 180 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.464-4882_464-4881i others(7): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404165 | ||||||
| chr5:123404257
|
C | G | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-4973G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404257 | ||||||
| chr5:123404299
|
C | G | 23 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(20): Show | 27 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.464-5015G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404299 | ||||||
| chr5:123404300
|
G | T | 161 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-5016C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404300 | ||||||
| chr5:123404327
|
C | T | 1 | a0001c0005t0003g0091 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.464-5043G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404327 | ||||||
| chr5:123404507
|
G | A | 5 | a0004c0004t0003g0051a0005c0007t0003g0086a0005c0007t0003g0087others(2): Show | 5 | HG02056.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-5223C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404507 | ||||||
| chr5:123404837
|
T | C | 1 | a0004c0004t0003g0062 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.464-5553A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404837 | ||||||
| chr5:123404876
|
C | A | 1 | a0003c0003t0001g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.464-5592G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404876 | ||||||
| chr5:123404992
|
T | C | 6 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0104others(3): Show | 8 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.464-5708A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404992 | ||||||
| chr5:123405012
|
C | G | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.464-5728G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405012 | ||||||
| chr5:123405079
|
A | C | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.464-5795T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405079 | ||||||
| chr5:123405094
|
T | C | 1 | a0001c0001t0002g0227 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.464-5810A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405094 | ||||||
| chr5:123405227
|
G | T | 71 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0005t0003g0011others(68): Show | 77 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.464-5943C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405227 | ||||||
| chr5:123405239
|
G | A | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.464-5955C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405239 | ||||||
| chr5:123405251
|
G | C | 1 | a0004c0004t0003g0046 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.464-5967C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405251 | ||||||
| chr5:123405277
|
A | AG | 327 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0014others(324): Show | 375 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.464-5994dupC | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405277 | ||||||
| chr5:123405431
|
T | C | 1 | a0002c0002t0001g0107 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.464-6147A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405431 | ||||||
| chr5:123405492
|
T | A | 28 | a0002c0002t0001g0019a0002c0002t0001g0095a0002c0002t0001g0143others(25): Show | 29 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.464-6208A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405492 | ||||||
| chr5:123405650
|
T | C | 157 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(154): Show | 177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.464-6366A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405650 | ||||||
| chr5:123405717
|
T | C | 157 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(154): Show | 177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.464-6433A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405717 | ||||||
| chr5:123405889
|
G | A | 3 | a0002c0002t0001g0112a0002c0002t0001g0122a0002c0002t0014g0124 | 3 | HG01081.hp1 HG01981.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.463+6510C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405889 | ||||||
| chr5:123406052
|
C | T | 142 | a0002c0002t0001g0005a0002c0002t0001g0016a0002c0002t0001g0017others(139): Show | 159 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.463+6347G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406052 | ||||||
| chr5:123406059
|
G | A | 2 | a0002c0002t0001g0122a0003c0003t0001g0299 | 2 | HG01981.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.463+6340C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406059 | ||||||
| chr5:123406060
|
A | T | 1 | a0002c0002t0001g0122 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.463+6339T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406060 | ||||||
| chr5:123406061
|
A | T | 1 | a0002c0002t0001g0122 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.463+6338T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406061 | ||||||
| chr5:123406062
|
T | C | 1 | a0002c0002t0001g0122 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.463+6337A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406062 | ||||||
| chr5:123406069
|
G | A | 2 | a0004c0004t0003g0060a0004c0004t0003g0061 | 2 | HG01891.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.463+6330C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406069 | ||||||
| chr5:123406178
|
GA | G | 229 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0321others(226): Show | 255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.463+6220delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406178 | ||||||
| chr5:123406227
|
A | G | 1 | a0001c0001t0002g0263 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.463+6172T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406227 | ||||||
| chr5:123406393
|
C | CA | 156 | a0001c0001t0004g0226a0001c0006t0002g0006a0001c0006t0002g0204others(153): Show | 176 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.463+6005dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406393 | ||||||
| chr5:123406479
|
C | T | 3 | a0002c0002t0001g0113a0002c0009t0001g0125a0002c0009t0010g0031 | 3 | HG00438.hp1 NA18984.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.463+5920G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406479 | ||||||
| chr5:123406482
|
GA | G | 157 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(154): Show | 177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.463+5916delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406482 | ||||||
| chr5:123406586
|
G | GA | 150 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0206others(147): Show | 169 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.463+5812dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406586 | ||||||
| chr5:123406586
|
G | GAA | 6 | a0001c0006t0002g0205a0001c0006t0008g0010a0001c0006t0009g0030others(3): Show | 7 | HG01975.hp2 HG02559.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.463+5811_463+5812d others(4): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406586 | ||||||
| chr5:123406586
|
GA | G | 35 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0230others(32): Show | 37 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.463+5812delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406586 | ||||||
| chr5:123406647
|
G | A | 37 | a0002c0002t0001g0005a0002c0002t0001g0016a0002c0002t0001g0017others(34): Show | 42 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.463+5752C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406647 | ||||||
| chr5:123406684
|
AG | A | 9 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(6): Show | 11 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.463+5714delC | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406684 | ||||||
| chr5:123406818
|
A | G | 1 | a0002c0002t0001g0131 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.463+5581T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406818 | ||||||
| chr5:123406852
|
G | A | 157 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(154): Show | 177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.463+5547C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406852 | ||||||
| chr5:123406908
|
T | G | 72 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0321others(69): Show | 78 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.463+5491A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406908 | ||||||
| chr5:123406961
|
G | A | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.463+5438C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406961 | ||||||
| chr5:123407105
|
T | TA | 142 | a0001c0001t0002g0227a0001c0006t0003g0322a0001c0006t0009g0030others(139): Show | 159 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.463+5293dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123407105 | ||||||
| chr5:123407105
|
T | TAA | 14 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(11): Show | 16 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.463+5292_463+5293d others(4): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123407105 | ||||||
| chr5:123407113
|
A | C | 1 | a0001c0001t0002g0263 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.463+5286T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123407113 | ||||||
| chr5:123407120
|
C | A | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.463+5279G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123407120 | ||||||
| chr5:123407276
|
G | A | 2 | a0002c0002t0001g0174a0002c0002t0001g0175 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.463+5123C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123407276 | ||||||
| chr5:123407370
|
C | T | 1 | a0001c0005t0003g0091 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.463+5029G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123407370 | ||||||
| chr5:123407548
|
C | T | 142 | a0002c0002t0001g0005a0002c0002t0001g0016a0002c0002t0001g0017others(139): Show | 159 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.463+4851G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123407548 | ||||||
| chr5:123407631
|
A | T | 157 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(154): Show | 177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.463+4768T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123407631 | ||||||
| chr5:123407683
|
T | C | 11 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(8): Show | 13 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.463+4716A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123407683 | ||||||
| chr5:123408035
|
G | C | 156 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(153): Show | 176 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.463+4364C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408035 | ||||||
| chr5:123408225
|
G | A | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.463+4174C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408225 | ||||||
| chr5:123408311
|
C | A | 156 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(153): Show | 176 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.463+4088G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408311 | ||||||
| chr5:123408433
|
T | C | 1 | a0002c0002t0001g0017 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.463+3966A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408433 | ||||||
| chr5:123408454
|
C | T | 1 | a0002c0002t0018g0328 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.463+3945G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408454 | ||||||
| chr5:123408484
|
T | C | 64 | a0002c0002t0001g0138a0002c0002t0001g0172a0002c0002t0001g0294others(61): Show | 75 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.463+3915A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408484 | ||||||
| chr5:123408525
|
T | C | 6 | a0005c0007t0003g0086a0005c0007t0003g0087a0005c0007t0003g0088others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.463+3874A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408525 | ||||||
| chr5:123408542
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3857T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408542 | ||||||
| chr5:123408548
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3851T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408548 | ||||||
| chr5:123408551
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3848T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408551 | ||||||
| chr5:123408568
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3831T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408568 | ||||||
| chr5:123408579
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3820T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408579 | ||||||
| chr5:123408585
|
T | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3814A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408585 | ||||||
| chr5:123408588
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3811T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408588 | ||||||
| chr5:123408589
|
T | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3810A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408589 | ||||||
| chr5:123408590
|
A | C | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3809T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408590 | ||||||
| chr5:123408608
|
A | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3791T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408608 | ||||||
| chr5:123408609
|
G | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3790C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408609 | ||||||
| chr5:123408611
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3788T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408611 | ||||||
| chr5:123408621
|
A | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3778T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408621 | ||||||
| chr5:123408623
|
A | T | 36 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0005t0003g0323others(33): Show | 38 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.463+3776T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408623 | ||||||
| chr5:123408628
|
A | C | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3771T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408628 | ||||||
| chr5:123408629
|
T | C | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3770A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408629 | ||||||
| chr5:123408631
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3768T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408631 | ||||||
| chr5:123408632
|
C | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3767G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408632 | ||||||
| chr5:123408632
|
C | T | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.463+3767G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408632 | ||||||
| chr5:123408636
|
C | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3763G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408636 | ||||||
| chr5:123408637
|
C | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3762G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408637 | ||||||
| chr5:123408638
|
C | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3761G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408638 | ||||||
| chr5:123408639
|
A | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3760T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408639 | ||||||
| chr5:123408640
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3759T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408640 | ||||||
| chr5:123408641
|
A | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3758T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408641 | ||||||
| chr5:123408642
|
C | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3757G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408642 | ||||||
| chr5:123408643
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3756T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408643 | ||||||
| chr5:123408647
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3752T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408647 | ||||||
| chr5:123408650
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3749T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408650 | ||||||
| chr5:123408651
|
C | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3748G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408651 | ||||||
| chr5:123408652
|
C | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3747G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408652 | ||||||
| chr5:123408677
|
C | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3722G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408677 | ||||||
| chr5:123408685
|
C | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3714G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408685 | ||||||
| chr5:123408686
|
A | C | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3713T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408686 | ||||||
| chr5:123408691
|
A | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3708T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408691 | ||||||
| chr5:123408692
|
G | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3707C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408692 | ||||||
| chr5:123408696
|
G | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3703C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408696 | ||||||
| chr5:123408697
|
A | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3702T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408697 | ||||||
| chr5:123408699
|
A | C | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3700T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408699 | ||||||
| chr5:123408702
|
A | C | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3697T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408702 | ||||||
| chr5:123408711
|
C | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3688G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408711 | ||||||
| chr5:123408764
|
C | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3635G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408764 | ||||||
| chr5:123408768
|
GAGGCCAG others(49): Show |
G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3575_463+3630d others(58): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408768 | ||||||
| chr5:123408826
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3573T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408826 | ||||||
| chr5:123408828
|
C | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3571G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408828 | ||||||
| chr5:123408832
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3567T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408832 | ||||||
| chr5:123408836
|
A | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3563T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408836 | ||||||
| chr5:123408841
|
C | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3558G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408841 | ||||||
| chr5:123408850
|
C | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3549G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408850 | ||||||
| chr5:123408858
|
C | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3541G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408858 | ||||||
| chr5:123408900
|
C | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3499G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408900 | ||||||
| chr5:123408910
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3489T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408910 | ||||||
| chr5:123408929
|
G | A | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.463+3470C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408929 | ||||||
| chr5:123408958
|
G | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3441C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408958 | ||||||
| chr5:123408961
|
C | CGTGTGTA others(31): Show |
1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3437_463+3438i others(40): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408961 | ||||||
| chr5:123408962
|
T | C | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3437A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408962 | ||||||
| chr5:123408965
|
G | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3434C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408965 | ||||||
| chr5:123408968
|
A | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3431T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408968 | ||||||
| chr5:123408984
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3415T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408984 | ||||||
| chr5:123408988
|
C | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3411G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408988 | ||||||
| chr5:123409112
|
C | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3287G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409112 | ||||||
| chr5:123409130
|
A | C | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.463+3269T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409130 | ||||||
| chr5:123409141
|
T | C | 1 | a0001c0005t0003g0084 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.463+3258A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409141 | ||||||
| chr5:123409231
|
C | A | 3 | a0003c0003t0001g0301a0003c0003t0001g0302a0003c0003t0001g0313 | 3 | HG00558.hp2 HG02071.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.463+3168G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409231 | ||||||
| chr5:123409297
|
A | G | 1 | a0001c0001t0006g0262 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.463+3102T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409297 | ||||||
| chr5:123409311
|
A | C | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3088T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409311 | ||||||
| chr5:123409313
|
C | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3086G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409313 | ||||||
| chr5:123409317
|
C | T | 40 | a0002c0002t0001g0005a0002c0002t0001g0016a0002c0002t0001g0017others(37): Show | 45 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.463+3082G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409317 | ||||||
| chr5:123409324
|
C | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3075G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409324 | ||||||
| chr5:123409328
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3071T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409328 | ||||||
| chr5:123409335
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3064T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409335 | ||||||
| chr5:123409336
|
A | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3063T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409336 | ||||||
| chr5:123409339
|
C | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3060G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409339 | ||||||
| chr5:123409340
|
C | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3059G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409340 | ||||||
| chr5:123409364
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3035T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409364 | ||||||
| chr5:123409563
|
A | C | 1 | a0002c0002t0001g0199 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.463+2836T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409563 | ||||||
| chr5:123409597
|
T | C | 157 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(154): Show | 177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.463+2802A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409597 | ||||||
| chr5:123409693
|
C | T | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.463+2706G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409693 | ||||||
| chr5:123409712
|
C | A | 1 | a0001c0001t0006g0290 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.463+2687G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409712 | ||||||
| chr5:123409762
|
G | A | 157 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(154): Show | 177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.463+2637C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409762 | ||||||
| chr5:123409779
|
G | A | 1 | a0004c0004t0003g0047 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.463+2620C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409779 | ||||||
| chr5:123409938
|
A | T | 1 | a0002c0002t0001g0130 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.463+2461T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409938 | ||||||
| chr5:123409953
|
C | G | 6 | a0001c0001t0002g0034a0001c0001t0002g0035a0004c0004t0003g0058others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.463+2446G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409953 | ||||||
| chr5:123409971
|
C | CA | 12 | a0001c0001t0002g0229a0001c0001t0002g0255a0001c0001t0002g0279others(9): Show | 12 | HG00140.hp2 HG01123.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.463+2427dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409971 | ||||||
| chr5:123409971
|
CA | C | 30 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(27): Show | 34 | HG00140.hp1 HG00323.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.463+2427delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409971 | ||||||
| chr5:123409989
|
A | ACCAC | 39 | a0002c0002t0001g0005a0002c0002t0001g0016a0002c0002t0001g0017others(36): Show | 44 | HG00438.hp1 HG00639.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.463+2409_463+2410i others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409989 | ||||||
| chr5:123409989
|
A | ACCACAC | 54 | a0002c0002t0001g0127a0002c0002t0001g0138a0002c0002t0001g0146others(51): Show | 63 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.463+2409_463+2410i others(8): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409989 | ||||||
| chr5:123409989
|
A | ACCACACA others(1): Show |
32 | a0002c0002t0001g0019a0002c0002t0001g0095a0002c0002t0001g0143others(29): Show | 33 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.463+2409_463+2410i others(10): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409989 | ||||||
| chr5:123409989
|
A | ACCACACA others(3): Show |
1 | a0003c0003t0001g0178 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.463+2409_463+2410i others(12): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409989 | ||||||
| chr5:123409991
|
A | C | 147 | a0001c0005t0005g0080a0001c0006t0008g0010a0001c0006t0009g0030others(144): Show | 165 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.463+2408T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409991 | ||||||
| chr5:123409992
|
C | A | 131 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0006t0002g0207others(128): Show | 146 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.463+2407G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409992 | ||||||
| chr5:123409992
|
C | CA | 3 | a0001c0005t0005g0080a0001c0006t0008g0010a0005c0007t0003g0087 | 4 | HG00738.hp1 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+2406_463+2407i others(3): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409992 | ||||||
| chr5:123409992
|
C | CACACA | 3 | a0002c0002t0001g0123a0002c0002t0001g0126a0002c0002t0001g0130 | 3 | HG00597.hp2 NA18972.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.463+2406_463+2407i others(7): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409992 | ||||||
| chr5:123409992
|
C | CACACACA | 10 | a0001c0006t0009g0030a0003c0003t0001g0021a0003c0003t0001g0022others(7): Show | 12 | HG01123.hp2 HG01891.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.463+2406_463+2407i others(9): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409992 | ||||||
| chr5:123409992
|
C | CACACACA others(2): Show |
3 | a0002c0002t0001g0169a0002c0002t0001g0201a0003c0003t0001g0307 | 3 | HG02148.hp2 HG03453.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.463+2406_463+2407i others(11): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409992 | ||||||
| chr5:123409992
|
C | CCA | 8 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(5): Show | 10 | HG01071.hp1 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.463+2405_463+2406d others(4): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409992 | ||||||
| chr5:123410039
|
A | G | 229 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0321others(226): Show | 255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.463+2360T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410039 | ||||||
| chr5:123410130
|
C | T | 1 | a0005c0007t0003g0086 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.463+2269G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410130 | ||||||
| chr5:123410188
|
T | C | 1 | a0003c0003t0001g0308 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.463+2211A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410188 | ||||||
| chr5:123410325
|
T | C | 1 | a0001c0001t0002g0257 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.463+2074A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410325 | ||||||
| chr5:123410372
|
G | T | 1 | a0001c0006t0002g0324 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.463+2027C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410372 | ||||||
| chr5:123410458
|
A | G | 157 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(154): Show | 177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.463+1941T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410458 | ||||||
| chr5:123410470
|
T | A | 23 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(20): Show | 27 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.463+1929A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410470 | ||||||
| chr5:123410470
|
T | C | 1 | a0001c0001t0002g0256 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.463+1929A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410470 | ||||||
| chr5:123410834
|
C | T | 229 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0321others(226): Show | 255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.463+1565G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410834 | ||||||
| chr5:123410969
|
A | G | 9 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(6): Show | 11 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.463+1430T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410969 | ||||||
| chr5:123411177
|
C | A | 141 | a0002c0002t0001g0005a0002c0002t0001g0016a0002c0002t0001g0017others(138): Show | 158 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.463+1222G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411177 | ||||||
| chr5:123411247
|
C | A | 72 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0005t0003g0011others(69): Show | 78 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.463+1152G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411247 | ||||||
| chr5:123411274
|
T | C | 1 | a0001c0005t0005g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.463+1125A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411274 | ||||||
| chr5:123411280
|
A | T | 1 | a0002c0002t0001g0148 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.463+1119T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411280 | ||||||
| chr5:123411283
|
G | A | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.463+1116C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411283 | ||||||
| chr5:123411301
|
C | A | 156 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(153): Show | 176 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.463+1098G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411301 | ||||||
| chr5:123411373
|
T | C | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.463+1026A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411373 | ||||||
| chr5:123411389
|
C | A | 2 | a0001c0006t0002g0204a0001c0006t0002g0205 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.463+1010G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411389 | ||||||
| chr5:123411634
|
A | G | 1 | a0007c0017t0002g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.463+765T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411634 | ||||||
| chr5:123411683
|
T | C | 2 | a0006c0010t0002g0202a0006c0010t0015g0033 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.463+716A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411683 | ||||||
| chr5:123411698
|
A | T | 1 | a0001c0005t0003g0090 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.463+701T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411698 | ||||||
| chr5:123412046
|
T | C | 4 | a0005c0007t0003g0086a0005c0007t0003g0087a0005c0007t0003g0088others(1): Show | 4 | HG02145.hp1 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.463+353A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123412046 | ||||||
| chr5:123412072
|
G | A | 3 | a0002c0002t0001g0211a0002c0002t0001g0212a0002c0002t0001g0213 | 3 | HG02055.hp2 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.463+327C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123412072 | ||||||
| chr5:123412151
|
A | G | 6 | a0001c0001t0002g0034a0001c0001t0002g0035a0004c0004t0003g0058others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.463+248T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123412151 | ||||||
| chr5:123412361
|
A | T | 8 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(5): Show | 10 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.463+38T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123412361 | ||||||
| chr5:123412595
|
T | C | 2 | a0001c0001t0002g0257a0001c0001t0002g0284 | 2 | HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.322-55A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123412595 | ||||||
| chr5:123412611
|
A | G | 7 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0216others(4): Show | 9 | NA18944.hp1 NA18946.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.322-71T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123412611 | ||||||
| chr5:123412655
|
A | AT | 38 | a0002c0002t0001g0019a0002c0002t0001g0095a0002c0002t0001g0143others(35): Show | 39 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.322-116dupA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123412655 | ||||||
| chr5:123412901
|
T | C | 2 | a0001c0006t0008g0010a0001c0006t0009g0030 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.322-361A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123412901 | ||||||
| chr5:123412913
|
C | T | 1 | a0001c0001t0002g0227 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.322-373G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123412913 | ||||||
| chr5:123412978
|
T | C | 3 | a0001c0001t0002g0027a0001c0001t0002g0258a0001c0001t0002g0259 | 4 | HG00639.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.322-438A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123412978 | ||||||
| chr5:123413032
|
C | G | 36 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081others(33): Show | 40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.322-492G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413032 | ||||||
| chr5:123413180
|
G | C | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.322-640C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413180 | ||||||
| chr5:123413248
|
A | C | 1 | a0001c0005t0003g0323 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.322-708T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413248 | ||||||
| chr5:123413265
|
C | A | 1 | a0001c0001t0002g0260 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.322-725G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413265 | ||||||
| chr5:123413270
|
C | A | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.322-730G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413270 | ||||||
| chr5:123413358
|
C | T | 15 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(12): Show | 17 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.322-818G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413358 | ||||||
| chr5:123413469
|
C | T | 1 | a0002c0002t0001g0199 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.322-929G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413469 | ||||||
| chr5:123413605
|
C | A | 228 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0005t0003g0011others(225): Show | 254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.322-1065G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413605 | ||||||
| chr5:123413914
|
C | G | 144 | a0001c0006t0008g0010a0001c0006t0009g0030a0002c0002t0001g0005others(141): Show | 162 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.322-1374G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413914 | ||||||
| chr5:123413947
|
G | A | 1 | a0003c0003t0001g0190 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.322-1407C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413947 | ||||||
| chr5:123414084
|
C | G | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.322-1544G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414084 | ||||||
| chr5:123414149
|
T | A | 1 | a0004c0004t0003g0052 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.322-1609A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414149 | ||||||
| chr5:123414233
|
G | C | 2 | a0004c0004t0003g0058a0004c0004t0003g0059 | 2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.322-1693C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414233 | ||||||
| chr5:123414409
|
T | G | 1 | a0003c0003t0001g0309 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.321+1601A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414409 | ||||||
| chr5:123414480
|
G | A | 1 | a0003c0003t0001g0179 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.321+1530C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414480 | ||||||
| chr5:123414527
|
T | C | 99 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0014others(96): Show | 121 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.321+1483A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414527 | ||||||
| chr5:123414538
|
A | G | 1 | a0003c0003t0001g0133 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.321+1472T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414538 | ||||||
| chr5:123414674
|
C | T | 35 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0005t0003g0323others(32): Show | 37 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.321+1336G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414674 | ||||||
| chr5:123414688
|
C | T | 1 | a0007c0017t0002g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.321+1322G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414688 | ||||||
| chr5:123414694
|
C | T | 35 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0005t0003g0323others(32): Show | 37 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.321+1316G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414694 | ||||||
| chr5:123414739
|
G | A | 3 | a0003c0003t0001g0310a0003c0003t0001g0311a0003c0003t0001g0314 | 3 | NA18939.hp1 NA18951.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.321+1271C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414739 | ||||||
| chr5:123414832
|
C | G | 18 | a0002c0002t0001g0138a0002c0002t0001g0172a0003c0003t0001g0020others(15): Show | 19 | HG00423.hp1 HG00597.hp1 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.321+1178G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414832 | ||||||
| chr5:123414840
|
C | T | 1 | a0002c0002t0001g0112 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.321+1170G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414840 | ||||||
| chr5:123414896
|
C | T | 2 | a0004c0004t0003g0058a0004c0004t0003g0059 | 2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.321+1114G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414896 | ||||||
| chr5:123414971
|
C | CA | 9 | a0001c0001t0002g0285a0001c0005t0005g0073a0001c0005t0005g0074others(6): Show | 9 | HG00140.hp1 HG00738.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.321+1038dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | ||||||
| chr5:123414971
|
C | CAAAAAAA others(3): Show |
1 | a0001c0006t0002g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.321+1029_321+1038d others(12): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | ||||||
| chr5:123414971
|
C | CAAAAAAA others(4): Show |
3 | a0001c0006t0002g0006a0001c0006t0002g0207a0001c0011t0002g0203 | 5 | HG01069.hp1 HG01071.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+1028_321+1038d others(13): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | ||||||
| chr5:123414971
|
C | CAAAAAAA others(5): Show |
2 | a0001c0006t0013g0208a0006c0010t0002g0202 | 2 | HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.321+1027_321+1038d others(14): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | ||||||
| chr5:123414971
|
C | CAAAAAAA others(12): Show |
1 | a0007c0017t0002g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.321+1020_321+1038d others(21): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | ||||||
| chr5:123414971
|
CA | C | 79 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0023others(76): Show | 99 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.321+1038delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | ||||||
| chr5:123414971
|
CAA | C | 11 | a0001c0001t0002g0034a0004c0004t0003g0037a0004c0004t0003g0053others(8): Show | 11 | HG00735.hp1 HG01891.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.321+1037_321+1038d others(4): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | ||||||
| chr5:123414971
|
CAAA | C | 25 | a0001c0001t0002g0035a0001c0005t0003g0323a0002c0002t0001g0095others(22): Show | 27 | HG00609.hp2 HG00733.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.321+1036_321+1038d others(5): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | ||||||
| chr5:123414971
|
CAAAAAA | C | 15 | a0001c0006t0002g0204a0001c0006t0002g0205a0001c0006t0008g0010others(12): Show | 16 | HG01891.hp2 HG02055.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+1033_321+1038d others(8): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | ||||||
| chr5:123414971
|
CAAAAAAA | C | 126 | a0001c0006t0002g0324a0002c0002t0001g0005a0002c0002t0001g0016others(123): Show | 143 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.321+1032_321+1038d others(9): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | ||||||
| chr5:123415020
|
G | A | 143 | a0001c0006t0008g0010a0001c0006t0009g0030a0002c0002t0001g0005others(140): Show | 161 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.321+990C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415020 | ||||||
| chr5:123415153
|
T | C | 101 | a0002c0002t0001g0019a0002c0002t0001g0138a0002c0002t0001g0143others(98): Show | 113 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.321+857A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415153 | ||||||
| chr5:123415172
|
A | G | 1 | a0001c0001t0004g0226 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.321+838T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415172 | ||||||
| chr5:123415173
|
G | C | 156 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(153): Show | 176 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.321+837C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415173 | ||||||
| chr5:123415212
|
A | T | 1 | a0002c0002t0001g0172 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.321+798T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415212 | ||||||
| chr5:123415278
|
A | C | 157 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(154): Show | 177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.321+732T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415278 | ||||||
| chr5:123415352
|
G | C | 2 | a0001c0006t0008g0010a0001c0006t0009g0030 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.321+658C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415352 | ||||||
| chr5:123415431
|
C | T | 2 | a0002c0002t0001g0174a0002c0002t0001g0175 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.321+579G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415431 | ||||||
| chr5:123415458
|
G | A | 1 | a0002c0002t0001g0111 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.321+552C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415458 | ||||||
| chr5:123415466
|
C | T | 3 | a0001c0005t0003g0011a0001c0005t0003g0063a0001c0005t0003g0081 | 4 | HG01255.hp2 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+544G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415466 | ||||||
| chr5:123415761
|
C | T | 28 | a0004c0004t0003g0013a0004c0004t0003g0015a0004c0004t0003g0037others(25): Show | 30 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.321+249G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415761 | ||||||
| chr5:123415809
|
T | C | 1 | a0005c0007t0003g0099 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.321+201A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415809 | ||||||
| chr5:123415829
|
G | A | 1 | a0003c0003t0001g0141 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.321+181C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415829 | ||||||
| chr5:123415864
|
T | A | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.321+146A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415864 | ||||||
| chr5:123415969
|
T | A | 1 | a0004c0004t0003g0015 | 2 | HG00733.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.321+41A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415969 | ||||||
| chr5:123415985
|
T | C | 2 | a0001c0001t0002g0286a0001c0001t0002g0287 | 2 | HG00621.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.321+25A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415985 | ||||||
| chr5:123416234
|
G | A | 1 | a0003c0003t0001g0193 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.207-110C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123416234 | ||||||
| chr5:123416400
|
A | G | 1 | a0002c0002t0001g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.207-276T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123416400 | ||||||
| chr5:123416436
|
T | C | 1 | a0004c0004t0003g0062 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.207-312A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123416436 | ||||||
| chr5:123416526
|
G | A | 1 | a0001c0001t0002g0288 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.207-402C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123416526 | ||||||
| chr5:123416602
|
AT | A | 7 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0104others(4): Show | 9 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.207-479delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123416602 | ||||||
| chr5:123416661
|
C | T | 1 | a0002c0008t0002g0217 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.207-537G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123416661 | ||||||
| chr5:123416916
|
C | T | 1 | a0002c0009t0010g0031 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.207-792G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123416916 | ||||||
| chr5:123416936
|
G | T | 36 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0005t0003g0323others(33): Show | 38 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.207-812C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123416936 | ||||||
| chr5:123417014
|
T | C | 11 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(8): Show | 13 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.207-890A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123417014 | ||||||
| chr5:123417173
|
A | G | 1 | a0004c0004t0003g0037 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.207-1049T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123417173 | ||||||
| chr5:123417250
|
A | G | 4 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(1): Show | 4 | HG02280.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.206+1109T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123417250 | ||||||
| chr5:123417296
|
CT | C | 101 | a0002c0002t0001g0019a0002c0002t0001g0138a0002c0002t0001g0143others(98): Show | 113 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.206+1062delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123417296 | ||||||
| chr5:123417467
|
A | G | 1 | a0002c0002t0001g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.206+892T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123417467 | ||||||
| chr5:123417727
|
C | T | 1 | a0002c0002t0001g0111 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.206+632G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123417727 | ||||||
| chr5:123417886
|
A | C | 159 | a0001c0001t0002g0225a0001c0006t0001g0103a0001c0006t0002g0006others(156): Show | 179 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.206+473T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123417886 | ||||||
| chr5:123418175
|
G | T | 4 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0223others(1): Show | 4 | HG00558.hp1 NA18982.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.206+184C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123418175 | ||||||
| chr5:123418224
|
T | TCTTA | 158 | a0001c0006t0001g0103a0001c0006t0002g0006a0001c0006t0002g0204others(155): Show | 178 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.206+134_206+135ins others(4): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123418224 | ||||||
| chr5:123418588
|
T | C | 2 | a0003c0003t0001g0022a0003c0003t0001g0195 | 3 | NA18959.hp1 NA18974.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.50-73A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123418588 | ||||||
| chr5:123418599
|
GT | G | 7 | a0001c0005t0003g0081a0002c0002t0001g0109a0002c0002t0001g0110others(4): Show | 7 | HG01243.hp2 HG01517.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-85delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123418599 | ||||||
| chr5:123418599
|
GTT | G | 148 | a0001c0006t0001g0103a0001c0006t0002g0006a0001c0006t0002g0204others(145): Show | 168 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.50-86_50-85delAA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123418599 | ||||||
| chr5:123418625
|
C | A | 13 | a0001c0005t0003g0082a0001c0005t0003g0083a0001c0005t0003g0084others(10): Show | 13 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.50-110G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123418625 | ||||||
| chr5:123418699
|
C | T | 2 | a0002c0002t0001g0143a0002c0002t0001g0144 | 2 | NA18960.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.50-184G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123418699 | ||||||
| chr5:123418722
|
A | G | 161 | a0001c0006t0001g0103a0001c0006t0002g0006a0001c0006t0002g0204others(158): Show | 181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.50-207T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123418722 | ||||||
| chr5:123418732
|
G | T | 7 | a0001c0006t0001g0103a0002c0002t0001g0016a0002c0002t0001g0017others(4): Show | 9 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.50-217C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123418732 | ||||||
| chr5:123418877
|
C | A | 1 | a0001c0001t0002g0029 | 2 | HG01109.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.50-362G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123418877 | ||||||
| chr5:123418919
|
T | C | 42 | a0001c0006t0001g0103a0001c0016t0002g0210a0002c0002t0001g0005others(39): Show | 47 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.50-404A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123418919 | ||||||
| chr5:123419066
|
C | T | 1 | a0001c0001t0002g0216 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.50-551G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419066 | ||||||
| chr5:123419346
|
A | C | 1 | a0001c0001t0002g0215 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.50-831T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419346 | ||||||
| chr5:123419347
|
G | A | 1 | a0001c0005t0005g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.50-832C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419347 | ||||||
| chr5:123419375
|
G | A | 12 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(9): Show | 14 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.50-860C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419375 | ||||||
| chr5:123419527
|
A | G | 159 | a0001c0001t0002g0214a0001c0006t0001g0103a0001c0006t0002g0006others(156): Show | 179 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.50-1012T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419527 | ||||||
| chr5:123419533
|
A | C | 1 | a0001c0005t0005g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.50-1018T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419533 | ||||||
| chr5:123419548
|
A | G | 1 | a0002c0002t0001g0102 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.50-1033T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419548 | ||||||
| chr5:123419553
|
C | CA | 7 | a0001c0001t0002g0289a0001c0006t0003g0322a0003c0003t0001g0291others(4): Show | 8 | HG01167.hp2 HG01192.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-1039dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419553 | ||||||
| chr5:123419553
|
C | CAA | 102 | a0001c0006t0001g0103a0001c0016t0002g0210a0002c0002t0001g0005others(99): Show | 117 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.50-1040_50-1039dup others(2): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419553 | ||||||
| chr5:123419553
|
C | CAAA | 5 | a0002c0002t0001g0132a0003c0003t0001g0022a0003c0003t0001g0194others(2): Show | 6 | NA18939.hp1 NA18950.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-1041_50-1039dup others(3): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419553 | ||||||
| chr5:123419555
|
A | AAC | 35 | a0002c0002t0001g0019a0002c0002t0001g0095a0002c0002t0001g0143others(32): Show | 36 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.50-1041_50-1040ins others(2): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419555 | ||||||
| chr5:123419556
|
A | AC | 2 | a0001c0006t0008g0010a0001c0006t0009g0030 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.50-1042_50-1041ins others(1): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419556 | ||||||
| chr5:123419558
|
A | AC | 10 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.50-1044_50-1043ins others(1): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419558 | ||||||
| chr5:123419640
|
G | A | 95 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0023others(92): Show | 116 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.50-1125C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419640 | ||||||
| chr5:123419658
|
T | G | 97 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0014others(94): Show | 119 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.50-1143A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419658 | ||||||
| chr5:123419708
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.50-1193A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419708 | ||||||
| chr5:123419782
|
C | T | 158 | a0001c0006t0001g0103a0001c0006t0002g0006a0001c0006t0002g0204others(155): Show | 178 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.50-1267G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419782 | ||||||
| chr5:123419868
|
C | T | 157 | a0001c0006t0001g0103a0001c0006t0002g0006a0001c0006t0002g0204others(154): Show | 177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.50-1353G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419868 | ||||||
| chr5:123419912
|
G | A | 158 | a0001c0006t0001g0103a0001c0006t0002g0006a0001c0006t0002g0204others(155): Show | 178 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.50-1397C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419912 | ||||||
| chr5:123419915
|
T | C | 1 | a0001c0005t0003g0096 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.50-1400A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419915 | ||||||
| chr5:123419945
|
G | T | 1 | a0002c0002t0001g0130 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.50-1430C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419945 | ||||||
| chr5:123420135
|
T | C | 2 | a0003c0003t0001g0196a0003c0003t0001g0197 | 2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.50-1620A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123420135 | ||||||
| chr5:123420434
|
T | C | 1 | a0002c0015t0001g0318 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.50-1919A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123420434 | ||||||
| chr5:123420567
|
G | A | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.50-2052C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123420567 | ||||||
| chr5:123420771
|
T | C | 1 | a0004c0004t0003g0097 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.49+2179A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123420771 | ||||||
| chr5:123420943
|
T | C | 1 | a0001c0006t0008g0010 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.49+2007A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123420943 | ||||||
| chr5:123420952
|
T | C | 11 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(8): Show | 13 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.49+1998A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123420952 | ||||||
| chr5:123420966
|
G | A | 4 | a0002c0002t0001g0005a0002c0002t0001g0130a0002c0002t0001g0131others(1): Show | 6 | HG02027.hp1 NA18950.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+1984C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123420966 | ||||||
| chr5:123420966
|
G | C | 4 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(1): Show | 4 | HG00323.hp1 HG00642.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+1984C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123420966 | ||||||
| chr5:123421295
|
C | T | 1 | a0001c0006t0008g0010 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.49+1655G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421295 | ||||||
| chr5:123421484
|
C | A | 1 | a0001c0001t0006g0290 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.49+1466G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421484 | ||||||
| chr5:123421548
|
T | C | 2 | a0005c0007t0003g0098a0005c0007t0003g0099 | 2 | HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.49+1402A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421548 | ||||||
| chr5:123421573
|
T | C | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.49+1377A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421573 | ||||||
| chr5:123421591
|
C | A | 10 | a0001c0006t0002g0006a0001c0006t0002g0204a0001c0006t0002g0205others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+1359G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421591 | ||||||
| chr5:123421743
|
T | C | 2 | a0001c0006t0008g0010a0001c0006t0009g0030 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.49+1207A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421743 | ||||||
| chr5:123421752
|
A | G | 254 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0023others(251): Show | 295 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.49+1198T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421752 | ||||||
| chr5:123421752
|
A | T | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.49+1198T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421752 | ||||||
| chr5:123421847
|
C | A | 1 | a0002c0002t0018g0328 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.49+1103G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421847 | ||||||
| chr5:123421907
|
T | C | 3 | a0002c0002t0001g0211a0002c0002t0001g0212a0002c0002t0001g0213 | 3 | HG02055.hp2 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.49+1043A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421907 | ||||||
| chr5:123421962
|
G | A | 1 | a0004c0004t0003g0015 | 2 | HG00733.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.49+988C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421962 | ||||||
| chr5:123422024
|
C | T | 157 | a0001c0006t0001g0103a0001c0006t0002g0006a0001c0006t0002g0204others(154): Show | 177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.49+926G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422024 | ||||||
| chr5:123422179
|
G | A | 26 | a0002c0002t0001g0294a0003c0003t0001g0002a0003c0003t0001g0003others(23): Show | 34 | HG00280.hp1 HG00558.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.49+771C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422179 | ||||||
| chr5:123422195
|
G | C | 1 | a0004c0004t0003g0100 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.49+755C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422195 | ||||||
| chr5:123422217
|
C | G | 1 | a0003c0003t0001g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.49+733G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422217 | ||||||
| chr5:123422326
|
C | G | 1 | a0003c0003t0001g0101 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.49+624G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422326 | ||||||
| chr5:123422438
|
T | TA | 4 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(1): Show | 4 | HG02280.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+511dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422438 | ||||||
| chr5:123422458
|
A | T | 9 | a0002c0002t0001g0138a0003c0003t0001g0133a0003c0003t0001g0134others(6): Show | 9 | HG00423.hp1 HG00597.hp1 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+492T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422458 | ||||||
| chr5:123422473
|
A | T | 38 | a0001c0006t0001g0103a0002c0002t0001g0005a0002c0002t0001g0016others(35): Show | 43 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.49+477T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422473 | ||||||
| chr5:123422551
|
G | A | 2 | a0001c0006t0008g0010a0001c0006t0009g0030 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.49+399C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422551 | ||||||
| chr5:123422574
|
G | C | 254 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0023others(251): Show | 295 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.49+376C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422574 | ||||||
| chr5:123422674
|
G | C | 2 | a0001c0006t0008g0010a0001c0006t0009g0030 | 3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.49+276C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422674 | ||||||
| chr5:123422719
|
G | A | 1 | a0003c0003t0001g0319 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.49+231C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422719 | ||||||
| chr5:123422756
|
T | C | 2 | a0001c0001t0002g0320a0001c0001t0002g0321 | 2 | NA18967.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.49+194A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422756 | ||||||
| chr5:123422793
|
G | T | 1 | a0006c0010t0015g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.49+157C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422793 | ||||||
| chr5:123422860
|
G | C | 1 | a0001c0006t0003g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.49+90C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422860 | ||||||
| chr5:123422869
|
G | A | 2 | a0001c0005t0003g0323a0001c0006t0002g0324 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.49+81C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422869 | ||||||
| chr5:123422920
|
A | T | 1 | a0002c0002t0001g0032 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.49+30T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422920 |