Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9859 |
|---|---|
| ensemblid | ENSG00000143702.16 |
| hgncid | 28920 |
| symbol | CEP170 |
| name | centrosomal protein 170 |
| refseq_nuc | NM_014812.3 |
| refseq_prot | NP_055627.2 |
| ensembl_nuc | ENST00000366542.6 |
| ensembl_prot | ENSP00000355500.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 243124428 |
| end | 243255281 |
| strand | - |
| ver | v1.2 |
| region | chr1:243124428-243255281 |
| region5000 | chr1:243119428-243260281 |
| regionname0 | CEP170_chr1_243124428_243255281 |
| regionname5000 | CEP170_chr1_243119428_243260281 |
| 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 | 0/0 | 1584 | 233 | 55 | 49 | 93 | 10 | 26 | 70 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0002 | 0/0 | 1584 | 37 | 15 | 9 | 10 | 2 | 1 | 7 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0003 | 0/0 | 1584 | 14 | 14 | 0 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0004 | 0/0 | 1584 | 7 | 1 | 6 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0005 | 0/1 | 1584 | 4 | 0 | 1 | 0 | 0 | 2 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0006 | 0/0 | 1584 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0007 | 0/0 | 1584 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0008 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0009 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0010 | 0/0 | 1584 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0011 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0012 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| 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 | 0/0 | 4755 | 225 | 51 | 49 | 89 | 10 | 26 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0002 | 0/0 | 4755 | 24 | 3 | 9 | 9 | 2 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0003 | 0/0 | 4755 | 12 | 12 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0004 | 0/0 | 4755 | 10 | 10 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0005 | 0/0 | 4755 | 7 | 1 | 6 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0006 | 0/1 | 4755 | 4 | 0 | 1 | 0 | 0 | 2 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0007 | 0/0 | 4755 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0008 | 0/0 | 4755 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0009 | 0/0 | 4755 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0010 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0011 | 0/0 | 4755 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0012 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0013 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0014 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0015 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0016 | 0/0 | 4755 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0017 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0018 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0019 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0020 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0021 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0022 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| c0023 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2305 | 230 | 57 | 56 | 77 | 10 | 29 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| t0002 | 0/0 | 2306 | 42 | 9 | 6 | 26 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| t0003 | 0/0 | 2306 | 18 | 17 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| t0004 | 0/0 | 2304 | 4 | 0 | 2 | 0 | 2 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| t0005 | 0/0 | 2305 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| t0006 | 0/0 | 2305 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| t0007 | 0/0 | 2305 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| t0008 | 0/0 | 2305 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| t0009 | 0/0 | 2305 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| t0010 | 0/0 | 2306 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| t0011 | 0/0 | 2306 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| t0012 | 0/0 | 2305 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0287 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| 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 | 0/0 | 4755 | 225 | 51 | 49 | 89 | 10 | 26 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0007 | 0/0 | 4755 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0010 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0013 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0014 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0015 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0023 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0002c0002 | 0/0 | 4755 | 24 | 3 | 9 | 9 | 2 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0002c0004 | 0/0 | 4755 | 10 | 10 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0002c0018 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0002c0019 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0002c0021 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0003c0003 | 0/0 | 4755 | 12 | 12 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0003c0009 | 0/0 | 4755 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0004c0005 | 0/0 | 4755 | 7 | 1 | 6 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0005c0006 | 0/1 | 4755 | 4 | 0 | 1 | 0 | 0 | 2 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0006c0008 | 0/0 | 4755 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0007c0011 | 0/0 | 4755 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0008c0020 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0009c0017 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0010c0016 | 0/0 | 4755 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0011c0012 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0012c0022 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7059 | 174 | 38 | 40 | 63 | 8 | 25 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0001t0002 | 0/0 | 7060 | 38 | 7 | 6 | 24 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0001t0003 | 0/0 | 7060 | 3 | 2 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0001t0004 | 0/0 | 7058 | 4 | 0 | 2 | 0 | 2 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0001t0005 | 0/0 | 7059 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0001t0008 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0001t0009 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0001t0010 | 0/0 | 7060 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0001t0011 | 0/0 | 7060 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0007t0001 | 0/0 | 7059 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0010t0002 | 0/0 | 7060 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0013t0001 | 0/0 | 7059 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0014t0001 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0015t0001 | 0/0 | 7059 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0001c0023t0002 | 0/0 | 7060 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0002c0002t0001 | 0/0 | 7059 | 22 | 2 | 8 | 9 | 2 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0002c0002t0003 | 0/0 | 7060 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0002c0002t0006 | 0/0 | 7059 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0002c0004t0001 | 0/0 | 7059 | 9 | 9 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0002c0004t0012 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0002c0018t0001 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0002c0019t0001 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0002c0021t0001 | 0/0 | 7059 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0003c0003t0003 | 0/0 | 7060 | 12 | 12 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0003c0009t0003 | 0/0 | 7060 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0004c0005t0001 | 0/0 | 7059 | 7 | 1 | 6 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0005c0006t0001 | 0/1 | 7059 | 4 | 0 | 1 | 0 | 0 | 2 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0006c0008t0002 | 0/0 | 7060 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0007c0011t0001 | 0/0 | 7059 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0008c0020t0001 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0009c0017t0007 | 0/0 | 7059 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0010c0016t0001 | 0/0 | 7059 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0011c0012t0001 | 0/0 | 7059 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| a0012c0022t0001 | 0/0 | 7059 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | copy fasta | chr1 | 243119428 | 243260281 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0008g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0010g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0001t0011g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0007t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0007t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0007t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0010t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0013t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0014t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0015t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0001c0023t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0002t0006g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0004t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0004t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0004t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0004t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0004t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0004t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0004t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0004t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0004t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0004t0012g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0018t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0019t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0002c0021t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0003c0003t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0003c0003t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0003c0003t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0003c0003t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0003c0003t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0003c0003t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0003c0003t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0003c0003t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0003c0003t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0003c0003t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0003c0003t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0003c0003t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0003c0009t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0003c0009t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0004c0005t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0004c0005t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0004c0005t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0004c0005t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0004c0005t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0004c0005t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0004c0005t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0005c0006t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0005c0006t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0005c0006t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0005c0006t0001g0287 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0006c0008t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0006c0008t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0007c0011t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0008c0020t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0009c0017t0007g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0010c0016t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0011c0012t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| a0012c0022t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | GBR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0180 | EUR | GBR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | FIN | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | CHS | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | CHS | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | CHS | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | CHS | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00735 | hp1 | a0004 | c0005 | t0001 | g0201 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01109 | hp2 | a0004 | c0005 | t0001 | g0197 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0163 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0184 | AMR | PUR | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0191 | AMR | CLM | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0183 | AMR | CLM | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0229 | AMR | CLM | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0290 | EUR | IBS | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0253 | EUR | IBS | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0003 | EUR | IBS | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0004 | EUR | IBS | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | IBS | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0004 | EUR | IBS | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01884 | hp1 | a0008 | c0020 | t0001 | g0125 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01884 | hp2 | a0003 | c0003 | t0003 | g0154 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0166 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01934 | hp1 | a0004 | c0005 | t0001 | g0192 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01952 | hp1 | a0004 | c0005 | t0001 | g0198 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01952 | hp2 | a0002 | c0002 | t0006 | g0181 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01975 | hp1 | a0010 | c0016 | t0001 | g0036 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01978 | hp1 | a0005 | c0006 | t0001 | g0233 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0178 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02004 | hp2 | a0004 | c0005 | t0001 | g0193 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02056 | hp1 | a0001 | c0015 | t0001 | g0223 | EAS | KHV | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | KHV | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02074 | hp1 | a0001 | c0013 | t0001 | g0023 | EAS | KHV | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | KHV | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02155 | hp1 | a0009 | c0017 | t0007 | g0037 | EAS | CDX | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CDX | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02257 | hp1 | a0002 | c0004 | t0001 | g0129 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02258 | hp1 | a0003 | c0003 | t0003 | g0150 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02280 | hp1 | a0006 | c0008 | t0002 | g0101 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0176 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02300 | hp1 | a0004 | c0005 | t0001 | g0199 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0169 | AMR | PEL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02451 | hp2 | a0003 | c0003 | t0003 | g0156 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02572 | hp2 | a0003 | c0003 | t0003 | g0161 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02615 | hp2 | a0003 | c0003 | t0003 | g0103 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02622 | hp1 | a0002 | c0018 | t0001 | g0122 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02647 | hp1 | a0002 | c0004 | t0001 | g0135 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02647 | hp2 | a0003 | c0003 | t0003 | g0157 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02723 | hp1 | a0003 | c0003 | t0003 | g0151 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02723 | hp2 | a0003 | c0009 | t0003 | g0109 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02809 | hp1 | a0001 | c0007 | t0001 | g0158 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02886 | hp2 | a0001 | c0014 | t0001 | g0110 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02895 | hp2 | a0002 | c0004 | t0001 | g0127 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02896 | hp1 | a0003 | c0003 | t0003 | g0153 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02897 | hp1 | a0002 | c0004 | t0001 | g0128 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02922 | hp1 | a0002 | c0004 | t0001 | g0134 | AFR | ESN | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02965 | hp1 | a0001 | c0007 | t0001 | g0099 | AFR | ESN | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0114 | AFR | ESN | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02976 | hp1 | a0001 | c0007 | t0001 | g0100 | AFR | ESN | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02976 | hp2 | a0002 | c0004 | t0001 | g0132 | AFR | ESN | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | ESN | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03195 | hp1 | a0003 | c0003 | t0003 | g0152 | AFR | ESN | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03225 | hp1 | a0001 | c0001 | t0009 | g0057 | AFR | MSL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | MSL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03453 | hp1 | a0006 | c0008 | t0002 | g0102 | AFR | MSL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03490 | hp2 | a0005 | c0006 | t0001 | g0234 | SAS | PJL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03540 | hp1 | a0002 | c0004 | t0012 | g0296 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03540 | hp2 | a0001 | c0001 | t0008 | g0104 | AFR | GWD | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | MSL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | STU | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | STU | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03942 | hp1 | a0007 | c0011 | t0001 | g0182 | SAS | BEB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | BEB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | STU | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0177 | SAS | STU | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG04228 | hp1 | a0005 | c0006 | t0001 | g0235 | SAS | STU | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | YRI | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | CHB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18747 | hp2 | a0012 | c0022 | t0001 | g0259 | EAS | CHB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18906 | hp1 | a0003 | c0003 | t0003 | g0155 | AFR | YRI | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0064 | AFR | YRI | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18946 | hp2 | a0002 | c0021 | t0001 | g0174 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18951 | hp2 | a0001 | c0001 | t0011 | g0295 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18990 | hp1 | a0011 | c0012 | t0001 | g0204 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19004 | hp2 | a0001 | c0010 | t0002 | g0263 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | LWK | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | LWK | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | LWK | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0185 | AFR | LWK | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19068 | hp1 | a0001 | c0001 | t0010 | g0215 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19090 | hp2 | a0001 | c0023 | t0002 | g0217 | EAS | JPT | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19240 | hp1 | a0003 | c0009 | t0003 | g0108 | AFR | YRI | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA19240 | hp2 | a0002 | c0004 | t0001 | g0130 | AFR | YRI | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | GIH | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | GIH | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02486 | hp1 | a0002 | c0019 | t0001 | g0131 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02559 | hp1 | a0002 | c0004 | t0001 | g0136 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG02559 | hp2 | a0002 | c0004 | t0001 | g0133 | AFR | ACB | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03471 | hp1 | a0002 | c0002 | t0003 | g0121 | AFR | MSL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | USA | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| HG06807 | hp2 | a0003 | c0003 | t0003 | g0107 | AFR | USA | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA20300 | hp1 | a0004 | c0005 | t0001 | g0196 | AFR | USA | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA20300 | hp2 | a0003 | c0003 | t0003 | g0149 | AFR | USA | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| homoSapiens_chm13v2 | hp1 | a0005 | c0006 | t0001 | g0287 | REF | REF | CEP170_chr1_243119428_243260281 | CEP170 | chr1 | 243119428 | 243260281 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:243156309
|
T | C | 1 | a0005 | 4 | HG01978.hp1 HG03490.hp2 HG04228.hp1 others(1): Show |
missense_variant | MODERATE | c.3823A>G | p.Met1275Val | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/20 | 4106/7059 | 3823/4755 | 1275/1584 | chr1 | 243156309 | ||
| chr1:243164434
|
C | T | 1 | a0006 | 2 | HG02280.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.3526G>A | p.Ala1176Thr | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/20 | 3809/7059 | 3526/4755 | 1176/1584 | chr1 | 243164434 | ||
| chr1:243169676
|
G | T | 1 | a0004 | 7 | HG00735.hp1 HG01109.hp2 HG01934.hp1 others(4): Show |
missense_variant | MODERATE | c.1795C>A | p.Gln599Lys | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/20 | 2078/7059 | 1795/4755 | 599/1584 | chr1 | 243169676 | ||
| chr1:243172783
|
G | C | 1 | a0008 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1630C>G | p.Leu544Val | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/20 | 1913/7059 | 1630/4755 | 544/1584 | chr1 | 243172783 | ||
| chr1:243186050
|
C | G | 1 | a0011 | 1 | NA18990.hp1 | missense_variant | MODERATE | c.1295G>C | p.Gly432Ala | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/20 | 1578/7059 | 1295/4755 | 432/1584 | chr1 | 243186050 | ||
| chr1:243186366
|
G | A | 1 | a0010 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.1165C>T | p.Arg389Cys | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 9/20 | 1448/7059 | 1165/4755 | 389/1584 | chr1 | 243186366 | ||
| chr1:243191267
|
T | C | 1 | a0009 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.859A>G | p.Ser287Gly | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/20 | 1142/7059 | 859/4755 | 287/1584 | chr1 | 243191267 | ||
| chr1:243191371
|
G | A | 1 | a0003 | 14 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(11): Show |
missense_variant | MODERATE | c.755C>T | p.Ser252Leu | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/20 | 1038/7059 | 755/4755 | 252/1584 | chr1 | 243191371 | ||
| chr1:243191489
|
C | T | 8 | a0001a0003a0004others(5): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
missense_variant | MODERATE | c.637G>A | p.Gly213Ser | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/20 | 920/7059 | 637/4755 | 213/1584 | chr1 | 243191489 | ||
| chr1:243200610
|
C | T | 1 | a0007 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.404G>A | p.Ser135Asn | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 6/20 | 687/7059 | 404/4755 | 135/1584 | chr1 | 243200610 | ||
| chr1:243221800
|
T | C | 1 | a0012 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.119A>G | p.Asp40Gly | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/20 | 402/7059 | 119/4755 | 40/1584 | chr1 | 243221800 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:243126485
|
G | A | 1 | a0002c0018 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.4719C>T | p.Pro1573Pro | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 20/20 | 5002/7059 | 4719/4755 | 1573/1584 | chr1 | 243126485 | ||
| chr1:243136199
|
G | A | 1 | a0001c0014 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.4263C>T | p.Val1421Val | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/20 | 4546/7059 | 4263/4755 | 1421/1584 | chr1 | 243136199 | ||
| chr1:243136202
|
G | A | 1 | a0001c0015 | 1 | HG02056.hp1 | synonymous_variant | LOW | c.4260C>T | p.Ser1420Ser | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/20 | 4543/7059 | 4260/4755 | 1420/1584 | chr1 | 243136202 | ||
| chr1:243164426
|
C | T | 1 | a0003c0009 | 2 | HG02723.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.3534G>A | p.Ser1178Ser | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/20 | 3817/7059 | 3534/4755 | 1178/1584 | chr1 | 243164426 | ||
| chr1:243165155
|
T | C | 2 | a0001c0007a0002c0019 | 4 | HG02486.hp1 HG02809.hp1 HG02965.hp1 others(1): Show |
synonymous_variant | LOW | c.2805A>G | p.Val935Val | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/20 | 3088/7059 | 2805/4755 | 935/1584 | chr1 | 243165155 | ||
| chr1:243165791
|
G | C | 2 | a0002c0004a0008c0020 | 11 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
synonymous_variant | LOW | c.2169C>G | p.Gly723Gly | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/20 | 2452/7059 | 2169/4755 | 723/1584 | chr1 | 243165791 | ||
| chr1:243165851
|
C | T | 1 | a0001c0013 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.2109G>A | p.Arg703Arg | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/20 | 2392/7059 | 2109/4755 | 703/1584 | chr1 | 243165851 | ||
| chr1:243186046
|
C | A | 1 | a0002c0021 | 1 | NA18946.hp2 | synonymous_variant | LOW | c.1299G>T | p.Gly433Gly | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/20 | 1582/7059 | 1299/4755 | 433/1584 | chr1 | 243186046 | ||
| chr1:243221742
|
A | G | 1 | a0001c0010 | 1 | NA19004.hp2 | synonymous_variant | LOW | c.177T>C | p.Asp59Asp | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/20 | 460/7059 | 177/4755 | 59/1584 | chr1 | 243221742 | ||
| chr1:243225269
|
T | C | 1 | a0001c0023 | 1 | NA19090.hp2 | synonymous_variant | LOW | c.12A>G | p.Thr4Thr | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/20 | 295/7059 | 12/4755 | 4/1584 | chr1 | 243225269 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:243124879
|
C | CT | 10 | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(7): Show | 62 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1569dupA | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 20/20 | 1569 | chr1 | 243124879 | |||||
| chr1:243124968
|
T | C | 1 | a0001c0001t0005 | 2 | HG02965.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1481A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 20/20 | 1481 | chr1 | 243124968 | |||||
| chr1:243125145
|
T | C | 7 | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(4): Show | 45 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1304A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 20/20 | 1304 | chr1 | 243125145 | |||||
| chr1:243125239
|
A | T | 1 | a0009c0017t0007 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1210T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 20/20 | 1210 | chr1 | 243125239 | |||||
| chr1:243125300
|
T | C | 1 | a0001c0001t0009 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1149A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 20/20 | 1149 | chr1 | 243125300 | |||||
| chr1:243125966
|
GT | G | 1 | a0001c0001t0004 | 4 | HG01257.hp1 HG01361.hp2 HG01516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*482delA | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 20/20 | 482 | chr1 | 243125966 | |||||
| chr1:243126175
|
A | G | 1 | a0002c0002t0006 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*274T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 20/20 | 274 | chr1 | 243126175 | |||||
| chr1:243126388
|
T | C | 1 | a0001c0001t0010 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*61A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 20/20 | 61 | chr1 | 243126388 | |||||
| chr1:243255136
|
G | C | 1 | a0001c0001t0011 | 1 | NA18951.hp2 | 5_prime_UTR_variant | MODIFIER | c.-138C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/20 | 29856 | chr1 | 243255136 | |||||
| chr1:243255213
|
C | A | 1 | a0002c0004t0012 | 1 | HG03540.hp1 | 5_prime_UTR_variant | MODIFIER | c.-215G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/20 | 29933 | chr1 | 243255213 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:243126883
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4466-145A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 19/19 | chr1 | 243126883 | ||||||
| chr1:243126957
|
T | C | 10 | a0002c0004t0001g0127a0002c0004t0001g0128a0002c0004t0001g0129others(7): Show | 10 | HG02257.hp1 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.4466-219A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 19/19 | chr1 | 243126957 | ||||||
| chr1:243126974
|
C | A | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG02735.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4466-236G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 19/19 | chr1 | 243126974 | ||||||
| chr1:243127001
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4466-263C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 19/19 | chr1 | 243127001 | ||||||
| chr1:243127231
|
G | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(2): Show | 6 | HG00140.hp2 HG00280.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.4466-493C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 19/19 | chr1 | 243127231 | ||||||
| chr1:243127252
|
T | C | 3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0111 | 3 | HG02451.hp1 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4466-514A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 19/19 | chr1 | 243127252 | ||||||
| chr1:243127269
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.4466-531G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 19/19 | chr1 | 243127269 | ||||||
| chr1:243127340
|
G | A | 69 | a0001c0001t0002g0009a0001c0001t0002g0062a0001c0001t0002g0081others(66): Show | 69 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.4466-602C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 19/19 | chr1 | 243127340 | ||||||
| chr1:243127401
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.4466-663G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 19/19 | chr1 | 243127401 | ||||||
| chr1:243127637
|
C | A | 1 | a0001c0001t0001g0016 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4465+612G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 19/19 | chr1 | 243127637 | ||||||
| chr1:243127793
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4465+456G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 19/19 | chr1 | 243127793 | ||||||
| chr1:243127928
|
T | C | 1 | a0002c0002t0003g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4465+321A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 19/19 | chr1 | 243127928 | ||||||
| chr1:243127981
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4465+268T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 19/19 | chr1 | 243127981 | ||||||
| chr1:243128077
|
T | G | 27 | a0001c0001t0001g0220a0002c0002t0001g0003a0002c0002t0001g0163others(24): Show | 28 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.4465+172A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 19/19 | chr1 | 243128077 | ||||||
| chr1:243128513
|
T | C | 1 | a0001c0001t0002g0009 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4414-213A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 18/19 | chr1 | 243128513 | ||||||
| chr1:243128539
|
A | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0106 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4414-239T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 18/19 | chr1 | 243128539 | ||||||
| chr1:243128607
|
C | A | 1 | a0001c0001t0002g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4414-307G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 18/19 | chr1 | 243128607 | ||||||
| chr1:243128717
|
C | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(84): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.4414-417G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 18/19 | chr1 | 243128717 | ||||||
| chr1:243128720
|
C | G | 1 | a0001c0001t0001g0044 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.4414-420G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 18/19 | chr1 | 243128720 | ||||||
| chr1:243128764
|
G | A | 2 | a0003c0009t0003g0108a0003c0009t0003g0109 | 2 | HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4414-464C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 18/19 | chr1 | 243128764 | ||||||
| chr1:243128846
|
C | T | 3 | a0001c0001t0003g0112a0001c0001t0003g0123a0001c0001t0003g0124 | 3 | HG01109.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4413+514G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 18/19 | chr1 | 243128846 | ||||||
| chr1:243128867
|
G | A | 1 | a0002c0004t0001g0134 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4413+493C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 18/19 | chr1 | 243128867 | ||||||
| chr1:243128975
|
T | C | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4413+385A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 18/19 | chr1 | 243128975 | ||||||
| chr1:243129101
|
A | G | 8 | a0001c0001t0002g0061a0001c0007t0001g0099a0001c0007t0001g0100others(5): Show | 8 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.4413+259T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 18/19 | chr1 | 243129101 | ||||||
| chr1:243129109
|
A | G | 1 | a0001c0001t0001g0244 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.4413+251T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 18/19 | chr1 | 243129109 | ||||||
| chr1:243129216
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4413+144T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 18/19 | chr1 | 243129216 | ||||||
| chr1:243129560
|
A | G | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.4320-107T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243129560 | ||||||
| chr1:243129747
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0040 | 3 | NA18982.hp1 NA18999.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.4320-294T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243129747 | ||||||
| chr1:243129759
|
C | T | 1 | a0001c0001t0001g0231 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.4320-306G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243129759 | ||||||
| chr1:243129864
|
G | C | 1 | a0001c0001t0001g0106 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4320-411C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243129864 | ||||||
| chr1:243129874
|
A | G | 73 | a0001c0001t0001g0106a0001c0001t0002g0009a0001c0001t0002g0061others(70): Show | 73 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.4320-421T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243129874 | ||||||
| chr1:243130794
|
G | A | 15 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(12): Show | 15 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.4320-1341C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243130794 | ||||||
| chr1:243130796
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4320-1343C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243130796 | ||||||
| chr1:243131079
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4320-1626A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243131079 | ||||||
| chr1:243131321
|
G | A | 2 | a0002c0004t0001g0135a0002c0004t0001g0136 | 2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.4320-1868C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243131321 | ||||||
| chr1:243131564
|
T | C | 1 | a0002c0021t0001g0174 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.4320-2111A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243131564 | ||||||
| chr1:243131932
|
C | G | 3 | a0001c0007t0001g0099a0001c0007t0001g0100a0002c0019t0001g0131 | 3 | HG02486.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4320-2479G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243131932 | ||||||
| chr1:243132240
|
C | T | 2 | a0002c0004t0001g0135a0002c0004t0001g0136 | 2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.4320-2787G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243132240 | ||||||
| chr1:243132310
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.4320-2857G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243132310 | ||||||
| chr1:243132493
|
T | A | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.4320-3040A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243132493 | ||||||
| chr1:243132695
|
C | CA | 25 | a0002c0002t0001g0003a0002c0002t0001g0163a0002c0002t0001g0164others(22): Show | 26 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.4320-3243dupT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243132695 | ||||||
| chr1:243132833
|
G | C | 7 | a0004c0005t0001g0192a0004c0005t0001g0193a0004c0005t0001g0196others(4): Show | 7 | HG00735.hp1 HG01109.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.4319+3310C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243132833 | ||||||
| chr1:243133162
|
T | C | 15 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(12): Show | 15 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.4319+2981A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243133162 | ||||||
| chr1:243133286
|
A | C | 11 | a0001c0001t0001g0106a0002c0004t0001g0127a0002c0004t0001g0128others(8): Show | 11 | HG02257.hp1 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.4319+2857T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243133286 | ||||||
| chr1:243133775
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.4319+2368A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243133775 | ||||||
| chr1:243133939
|
A | G | 1 | a0001c0001t0001g0284 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.4319+2204T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243133939 | ||||||
| chr1:243133981
|
A | G | 89 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.4319+2162T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243133981 | ||||||
| chr1:243134095
|
T | C | 74 | a0001c0001t0001g0060a0001c0001t0001g0097a0001c0001t0001g0098others(71): Show | 74 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.4319+2048A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243134095 | ||||||
| chr1:243134324
|
T | A | 1 | a0001c0001t0001g0228 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4319+1819A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243134324 | ||||||
| chr1:243134622
|
C | G | 26 | a0002c0002t0001g0003a0002c0002t0001g0163a0002c0002t0001g0164others(23): Show | 27 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.4319+1521G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243134622 | ||||||
| chr1:243134651
|
C | G | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4319+1492G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243134651 | ||||||
| chr1:243134664
|
AT | A | 11 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0066others(8): Show | 11 | HG00099.hp1 HG01168.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.4319+1478delA | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243134664 | ||||||
| chr1:243134688
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4319+1455G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243134688 | ||||||
| chr1:243134692
|
C | T | 1 | a0001c0001t0001g0281 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4319+1451G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243134692 | ||||||
| chr1:243134736
|
C | T | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4319+1407G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243134736 | ||||||
| chr1:243134799
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4319+1344G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243134799 | ||||||
| chr1:243134876
|
C | T | 10 | a0002c0004t0001g0127a0002c0004t0001g0128a0002c0004t0001g0129others(7): Show | 10 | HG02257.hp1 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.4319+1267G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243134876 | ||||||
| chr1:243134955
|
C | T | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.4319+1188G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243134955 | ||||||
| chr1:243135300
|
G | A | 12 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(9): Show | 12 | HG00408.hp2 HG01934.hp2 NA18940.hp1 others(9): Show |
intron_variant | MODIFIER | c.4319+843C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243135300 | ||||||
| chr1:243135344
|
C | T | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(20): Show | 23 | HG00099.hp2 HG00609.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.4319+799G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243135344 | ||||||
| chr1:243135351
|
C | T | 27 | a0001c0001t0001g0220a0002c0002t0001g0003a0002c0002t0001g0163others(24): Show | 28 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.4319+792G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243135351 | ||||||
| chr1:243135388
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.4319+755T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243135388 | ||||||
| chr1:243135528
|
A | G | 34 | a0001c0001t0001g0106a0001c0001t0001g0115a0001c0001t0001g0116others(31): Show | 35 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.4319+615T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243135528 | ||||||
| chr1:243135647
|
C | T | 2 | a0001c0001t0001g0220a0007c0011t0001g0182 | 2 | HG01891.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.4319+496G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243135647 | ||||||
| chr1:243135884
|
T | A | 11 | a0003c0003t0003g0103a0003c0003t0003g0149a0003c0003t0003g0150others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.4319+259A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243135884 | ||||||
| chr1:243135981
|
C | G | 10 | a0002c0004t0001g0127a0002c0004t0001g0128a0002c0004t0001g0129others(7): Show | 10 | HG02257.hp1 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.4319+162G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243135981 | ||||||
| chr1:243135981
|
C | T | 2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | NA18964.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.4319+162G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243135981 | ||||||
| chr1:243135986
|
A | C | 1 | a0001c0001t0001g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4319+157T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243135986 | ||||||
| chr1:243135996
|
T | G | 2 | a0002c0004t0001g0135a0002c0004t0001g0136 | 2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.4319+147A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243135996 | ||||||
| chr1:243136134
|
T | A | 24 | a0002c0002t0001g0003a0002c0002t0001g0163a0002c0002t0001g0164others(21): Show | 25 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.4319+9A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 17/19 | chr1 | 243136134 | ||||||
| chr1:243136651
|
C | T | 10 | a0002c0004t0001g0127a0002c0004t0001g0128a0002c0004t0001g0129others(7): Show | 10 | HG02257.hp1 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.4231-420G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243136651 | ||||||
| chr1:243136879
|
T | C | 10 | a0002c0004t0001g0127a0002c0004t0001g0128a0002c0004t0001g0129others(7): Show | 10 | HG02257.hp1 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.4231-648A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243136879 | ||||||
| chr1:243137017
|
G | C | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4231-786C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243137017 | ||||||
| chr1:243137128
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.4231-897A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243137128 | ||||||
| chr1:243137466
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4231-1235C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243137466 | ||||||
| chr1:243137541
|
C | T | 1 | a0001c0001t0002g0216 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.4231-1310G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243137541 | ||||||
| chr1:243137543
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4231-1312C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243137543 | ||||||
| chr1:243137647
|
T | C | 6 | a0001c0001t0001g0055a0001c0007t0001g0099a0001c0007t0001g0100others(3): Show | 6 | HG01884.hp1 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.4231-1416A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243137647 | ||||||
| chr1:243137779
|
T | TA | 6 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(3): Show | 6 | HG00741.hp1 HG01109.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.4231-1549dupT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243137779 | ||||||
| chr1:243137779
|
TA | T | 11 | a0001c0001t0001g0228a0001c0001t0003g0112a0002c0004t0001g0127others(8): Show | 11 | HG02155.hp2 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.4231-1549delT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243137779 | ||||||
| chr1:243137839
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.4231-1608T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243137839 | ||||||
| chr1:243137901
|
G | A | 3 | a0001c0001t0003g0112a0001c0001t0003g0123a0001c0001t0003g0124 | 3 | HG01109.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4231-1670C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243137901 | ||||||
| chr1:243137943
|
G | A | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4231-1712C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243137943 | ||||||
| chr1:243138060
|
T | C | 1 | a0001c0001t0002g0083 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4231-1829A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243138060 | ||||||
| chr1:243138296
|
C | A | 1 | a0001c0001t0002g0093 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4230+1641G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243138296 | ||||||
| chr1:243138387
|
A | G | 16 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(13): Show | 16 | HG01981.hp1 HG02257.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.4230+1550T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243138387 | ||||||
| chr1:243138506
|
C | G | 1 | a0001c0001t0002g0261 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.4230+1431G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243138506 | ||||||
| chr1:243138621
|
T | C | 1 | a0002c0002t0006g0181 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.4230+1316A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243138621 | ||||||
| chr1:243138914
|
C | G | 1 | a0001c0001t0001g0264 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4230+1023G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243138914 | ||||||
| chr1:243139125
|
A | G | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.4230+812T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243139125 | ||||||
| chr1:243139155
|
G | A | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.4230+782C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243139155 | ||||||
| chr1:243139159
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4230+778A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243139159 | ||||||
| chr1:243139252
|
C | T | 1 | a0001c0014t0001g0110 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4230+685G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243139252 | ||||||
| chr1:243139493
|
TGTATTTC others(95): Show |
T | 2 | a0001c0007t0001g0158a0008c0020t0001g0125 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4230+342_4230+443d others(2): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243139493 | ||||||
| chr1:243139586
|
T | C | 12 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(9): Show | 12 | HG00408.hp2 HG01934.hp2 NA18940.hp1 others(9): Show |
intron_variant | MODIFIER | c.4230+351A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243139586 | ||||||
| chr1:243139761
|
C | T | 10 | a0002c0004t0001g0127a0002c0004t0001g0128a0002c0004t0001g0129others(7): Show | 10 | HG02257.hp1 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.4230+176G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 16/19 | chr1 | 243139761 | ||||||
| chr1:243140239
|
T | A | 1 | a0001c0001t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4060-132A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 15/19 | chr1 | 243140239 | ||||||
| chr1:243140345
|
T | C | 1 | a0001c0001t0002g0226 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.4060-238A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 15/19 | chr1 | 243140345 | ||||||
| chr1:243140396
|
T | C | 59 | a0001c0001t0002g0009a0001c0001t0002g0061a0001c0001t0002g0062others(56): Show | 59 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.4060-289A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 15/19 | chr1 | 243140396 | ||||||
| chr1:243140421
|
A | T | 1 | a0011c0012t0001g0204 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.4060-314T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 15/19 | chr1 | 243140421 | ||||||
| chr1:243140486
|
T | C | 59 | a0001c0001t0002g0009a0001c0001t0002g0061a0001c0001t0002g0062others(56): Show | 59 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.4060-379A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 15/19 | chr1 | 243140486 | ||||||
| chr1:243140710
|
T | C | 59 | a0001c0001t0002g0009a0001c0001t0002g0061a0001c0001t0002g0062others(56): Show | 59 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.4060-603A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 15/19 | chr1 | 243140710 | ||||||
| chr1:243140813
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.4060-706C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 15/19 | chr1 | 243140813 | ||||||
| chr1:243141080
|
C | T | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.4060-973G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 15/19 | chr1 | 243141080 | ||||||
| chr1:243141364
|
A | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(87): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.4059+952T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 15/19 | chr1 | 243141364 | ||||||
| chr1:243141405
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4059+911G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 15/19 | chr1 | 243141405 | ||||||
| chr1:243141743
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4059+573A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 15/19 | chr1 | 243141743 | ||||||
| chr1:243141834
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4059+482T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 15/19 | chr1 | 243141834 | ||||||
| chr1:243141844
|
G | T | 1 | a0001c0001t0001g0249 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4059+472C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 15/19 | chr1 | 243141844 | ||||||
| chr1:243141885
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4059+431C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 15/19 | chr1 | 243141885 | ||||||
| chr1:243142047
|
T | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0034others(5): Show | 8 | HG01975.hp1 HG01993.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.4059+269A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 15/19 | chr1 | 243142047 | ||||||
| chr1:243142145
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4059+171A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 15/19 | chr1 | 243142145 | ||||||
| chr1:243142571
|
T | C | 1 | a0001c0001t0001g0294 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3912-108A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243142571 | ||||||
| chr1:243142731
|
G | A | 10 | a0002c0004t0001g0127a0002c0004t0001g0128a0002c0004t0001g0129others(7): Show | 10 | HG02257.hp1 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3912-268C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243142731 | ||||||
| chr1:243142842
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3912-379G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243142842 | ||||||
| chr1:243142927
|
T | G | 3 | a0003c0003t0003g0107a0003c0009t0003g0108a0003c0009t0003g0109 | 3 | HG02723.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3912-464A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243142927 | ||||||
| chr1:243142960
|
G | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG01891.hp1 HG02257.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3912-497C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243142960 | ||||||
| chr1:243143149
|
G | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(83): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.3912-686C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243143149 | ||||||
| chr1:243143173
|
G | C | 212 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(209): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.3912-710C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243143173 | ||||||
| chr1:243143500
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3912-1037T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243143500 | ||||||
| chr1:243143622
|
G | A | 212 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(209): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.3912-1159C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243143622 | ||||||
| chr1:243144956
|
C | T | 213 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(210): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.3912-2493G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243144956 | ||||||
| chr1:243145018
|
C | T | 11 | a0003c0003t0003g0103a0003c0003t0003g0149a0003c0003t0003g0150others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.3912-2555G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243145018 | ||||||
| chr1:243145072
|
T | A | 1 | a0001c0001t0001g0106 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3912-2609A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243145072 | ||||||
| chr1:243145102
|
T | G | 59 | a0001c0001t0002g0009a0001c0001t0002g0061a0001c0001t0002g0062others(56): Show | 59 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.3912-2639A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243145102 | ||||||
| chr1:243145106
|
A | C | 59 | a0001c0001t0002g0009a0001c0001t0002g0061a0001c0001t0002g0062others(56): Show | 59 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.3912-2643T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243145106 | ||||||
| chr1:243145202
|
A | G | 1 | a0001c0014t0001g0110 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3912-2739T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243145202 | ||||||
| chr1:243145331
|
G | C | 4 | a0005c0006t0001g0233a0005c0006t0001g0234a0005c0006t0001g0235others(1): Show | 4 | HG01978.hp1 HG03490.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.3912-2868C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243145331 | ||||||
| chr1:243145418
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3912-2955C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243145418 | ||||||
| chr1:243145420
|
G | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG01891.hp1 HG02257.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3912-2957C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243145420 | ||||||
| chr1:243145435
|
C | T | 1 | a0001c0001t0005g0114 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3912-2972G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243145435 | ||||||
| chr1:243145593
|
G | A | 69 | a0001c0001t0002g0009a0001c0001t0002g0062a0001c0001t0002g0081others(66): Show | 69 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.3912-3130C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243145593 | ||||||
| chr1:243145688
|
A | G | 1 | a0001c0001t0002g0256 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3912-3225T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243145688 | ||||||
| chr1:243145711
|
A | T | 1 | a0001c0001t0001g0052 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3912-3248T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243145711 | ||||||
| chr1:243145712
|
A | T | 1 | a0001c0001t0001g0052 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3912-3249T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243145712 | ||||||
| chr1:243145889
|
A | G | 57 | a0001c0001t0002g0009a0001c0001t0002g0061a0001c0001t0002g0062others(54): Show | 57 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.3912-3426T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243145889 | ||||||
| chr1:243146188
|
G | A | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG02735.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3912-3725C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243146188 | ||||||
| chr1:243146199
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0106 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3912-3736T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243146199 | ||||||
| chr1:243146284
|
T | C | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3912-3821A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243146284 | ||||||
| chr1:243146357
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3912-3894C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243146357 | ||||||
| chr1:243146656
|
G | A | 26 | a0002c0002t0001g0003a0002c0002t0001g0163a0002c0002t0001g0164others(23): Show | 27 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.3912-4193C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243146656 | ||||||
| chr1:243146681
|
A | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.3912-4218T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243146681 | ||||||
| chr1:243146765
|
C | A | 1 | a0002c0002t0003g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3912-4302G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243146765 | ||||||
| chr1:243146884
|
TC | T | 3 | a0005c0006t0001g0234a0005c0006t0001g0235a0005c0006t0001g0287 | 3 | HG03490.hp2 HG04228.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3912-4422delG | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243146884 | ||||||
| chr1:243146893
|
T | TCCCTAAC others(24): Show |
1 | a0001c0001t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3912-4461_3912-443 others(35): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243146893 | ||||||
| chr1:243146905
|
G | GAAGACCA others(24): Show |
13 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0055others(10): Show | 13 | HG01099.hp1 HG02451.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.3912-4473_3912-444 others(35): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243146905 | ||||||
| chr1:243146905
|
G | GAAGACCA others(86): Show |
1 | a0001c0001t0001g0050 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3912-4443_3912-444 others(97): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243146905 | ||||||
| chr1:243146905
|
GAAGACCA others(24): Show |
G | 13 | a0001c0001t0001g0094a0001c0001t0002g0105a0003c0003t0003g0103others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.3912-4473_3912-444 others(35): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243146905 | ||||||
| chr1:243147061
|
C | T | 55 | a0001c0001t0002g0009a0001c0001t0002g0062a0001c0001t0002g0081others(52): Show | 55 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.3912-4598G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243147061 | ||||||
| chr1:243147386
|
C | T | 1 | a0001c0001t0002g0269 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3912-4923G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243147386 | ||||||
| chr1:243147809
|
G | C | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.3912-5346C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243147809 | ||||||
| chr1:243147826
|
T | G | 1 | a0002c0002t0001g0170 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3912-5363A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243147826 | ||||||
| chr1:243148051
|
C | T | 1 | a0001c0001t0010g0215 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3912-5588G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243148051 | ||||||
| chr1:243148052
|
G | A | 8 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0094others(5): Show | 8 | HG02451.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.3912-5589C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243148052 | ||||||
| chr1:243148297
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0248 | 2 | HG01192.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.3912-5834C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243148297 | ||||||
| chr1:243148481
|
C | T | 56 | a0001c0001t0002g0009a0001c0001t0002g0062a0001c0001t0002g0081others(53): Show | 56 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.3912-6018G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243148481 | ||||||
| chr1:243148606
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3912-6143C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243148606 | ||||||
| chr1:243148643
|
C | G | 3 | a0003c0003t0003g0107a0003c0009t0003g0108a0003c0009t0003g0109 | 3 | HG02723.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3912-6180G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243148643 | ||||||
| chr1:243148801
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG02004.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.3912-6338C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243148801 | ||||||
| chr1:243149110
|
T | C | 11 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(8): Show | 11 | HG00438.hp1 HG00597.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.3912-6647A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243149110 | ||||||
| chr1:243149161
|
G | GA | 90 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(87): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.3912-6699dupT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243149161 | ||||||
| chr1:243149339
|
T | A | 66 | a0001c0001t0001g0106a0001c0001t0001g0115a0001c0001t0001g0116others(63): Show | 66 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.3912-6876A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243149339 | ||||||
| chr1:243149903
|
G | T | 60 | a0001c0001t0001g0106a0001c0001t0002g0009a0001c0001t0002g0062others(57): Show | 60 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.3911+6318C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243149903 | ||||||
| chr1:243150156
|
T | C | 4 | a0001c0001t0001g0239a0001c0001t0001g0281a0001c0001t0001g0283others(1): Show | 4 | HG02027.hp2 NA18962.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.3911+6065A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243150156 | ||||||
| chr1:243150229
|
C | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0097others(2): Show | 5 | HG02451.hp1 HG02922.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.3911+5992G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243150229 | ||||||
| chr1:243150237
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3911+5984C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243150237 | ||||||
| chr1:243150416
|
C | T | 3 | a0001c0007t0001g0099a0001c0007t0001g0100a0002c0019t0001g0131 | 3 | HG02486.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3911+5805G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243150416 | ||||||
| chr1:243150445
|
C | G | 1 | a0001c0001t0001g0040 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3911+5776G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243150445 | ||||||
| chr1:243150479
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3911+5742A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243150479 | ||||||
| chr1:243150583
|
C | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.3911+5638G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243150583 | ||||||
| chr1:243150606
|
C | T | 6 | a0001c0001t0002g0205a0001c0001t0002g0218a0001c0001t0002g0226others(3): Show | 6 | HG02083.hp2 HG02523.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.3911+5615G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243150606 | ||||||
| chr1:243150608
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3911+5613C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243150608 | ||||||
| chr1:243150715
|
A | T | 67 | a0001c0001t0001g0106a0001c0001t0001g0115a0001c0001t0001g0116others(64): Show | 67 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.3911+5506T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243150715 | ||||||
| chr1:243150815
|
G | C | 2 | a0002c0002t0001g0168a0002c0002t0001g0179 | 2 | NA19000.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.3911+5406C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243150815 | ||||||
| chr1:243150863
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3911+5358A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243150863 | ||||||
| chr1:243150866
|
C | T | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3911+5355G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243150866 | ||||||
| chr1:243150891
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3911+5330T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243150891 | ||||||
| chr1:243151007
|
T | C | 1 | a0002c0002t0001g0185 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3911+5214A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243151007 | ||||||
| chr1:243151275
|
T | C | 212 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(209): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.3911+4946A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243151275 | ||||||
| chr1:243151505
|
G | C | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3911+4716C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243151505 | ||||||
| chr1:243151554
|
T | C | 34 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(31): Show | 34 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.3911+4667A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243151554 | ||||||
| chr1:243151959
|
T | C | 1 | a0001c0001t0003g0123 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3911+4262A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243151959 | ||||||
| chr1:243152038
|
A | C | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3911+4183T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243152038 | ||||||
| chr1:243152062
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3911+4159G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243152062 | ||||||
| chr1:243152135
|
C | T | 2 | a0003c0009t0003g0108a0003c0009t0003g0109 | 2 | HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3911+4086G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243152135 | ||||||
| chr1:243152248
|
G | T | 56 | a0001c0001t0002g0009a0001c0001t0002g0061a0001c0001t0002g0062others(53): Show | 56 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.3911+3973C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243152248 | ||||||
| chr1:243152323
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3911+3898C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243152323 | ||||||
| chr1:243152415
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3911+3806C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243152415 | ||||||
| chr1:243152424
|
T | C | 6 | a0002c0004t0001g0127a0002c0004t0001g0128a0002c0004t0001g0129others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3911+3797A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243152424 | ||||||
| chr1:243152521
|
A | AT | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): Show | 110 | HG00280.hp2 HG00597.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.3911+3699dupA | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243152521 | ||||||
| chr1:243152521
|
A | ATT | 48 | a0001c0001t0001g0120a0001c0001t0001g0195a0001c0001t0001g0206others(45): Show | 48 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.3911+3698_3911+369 others(6): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243152521 | ||||||
| chr1:243152521
|
A | ATTT | 30 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0021others(27): Show | 30 | HG00099.hp2 HG00558.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.3911+3697_3911+369 others(7): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243152521 | ||||||
| chr1:243152521
|
A | ATTTT | 36 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(33): Show | 37 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.3911+3696_3911+369 others(8): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243152521 | ||||||
| chr1:243152521
|
A | ATTTTT | 26 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(23): Show | 26 | HG00639.hp2 HG00733.hp1 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.3911+3695_3911+369 others(9): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243152521 | ||||||
| chr1:243152521
|
ATTTTTTT others(3): Show |
A | 37 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(34): Show | 38 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.3911+3690_3911+369 others(14): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243152521 | ||||||
| chr1:243152521
|
ATTTTTTT others(5): Show |
A | 1 | a0002c0002t0003g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3911+3688_3911+369 others(16): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243152521 | ||||||
| chr1:243152656
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | NA19002.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.3911+3565G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243152656 | ||||||
| chr1:243152827
|
G | A | 1 | a0002c0004t0001g0136 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3911+3394C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243152827 | ||||||
| chr1:243153162
|
T | A | 2 | a0001c0001t0005g0064a0001c0001t0005g0114 | 2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3911+3059A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243153162 | ||||||
| chr1:243153238
|
A | C | 1 | a0001c0001t0003g0124 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3911+2983T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243153238 | ||||||
| chr1:243153264
|
G | A | 1 | a0002c0002t0001g0170 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3911+2957C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243153264 | ||||||
| chr1:243153726
|
G | GA | 8 | a0001c0001t0001g0106a0001c0001t0001g0115a0001c0001t0001g0116others(5): Show | 8 | HG01891.hp2 HG01981.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.3911+2494dupT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243153726 | ||||||
| chr1:243153770
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3911+2451A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243153770 | ||||||
| chr1:243154126
|
C | G | 1 | a0001c0001t0001g0060 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3911+2095G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243154126 | ||||||
| chr1:243154393
|
T | G | 1 | a0001c0001t0002g0187 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3911+1828A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243154393 | ||||||
| chr1:243154431
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3911+1790G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243154431 | ||||||
| chr1:243154555
|
T | C | 1 | a0001c0010t0002g0263 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.3911+1666A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243154555 | ||||||
| chr1:243154599
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3911+1622A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243154599 | ||||||
| chr1:243154620
|
G | A | 1 | a0001c0014t0001g0110 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3911+1601C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243154620 | ||||||
| chr1:243155187
|
G | A | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG02735.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3911+1034C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243155187 | ||||||
| chr1:243155358
|
TTTC | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(83): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.3911+860_3911+862d others(5): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243155358 | ||||||
| chr1:243155821
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3911+400T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243155821 | ||||||
| chr1:243155849
|
C | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(83): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.3911+372G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243155849 | ||||||
| chr1:243155953
|
T | C | 87 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(84): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.3911+268A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243155953 | ||||||
| chr1:243155986
|
G | A | 4 | a0001c0001t0001g0195a0001c0001t0001g0213a0001c0001t0001g0241others(1): Show | 4 | HG00741.hp2 HG01123.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.3911+235C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243155986 | ||||||
| chr1:243156048
|
A | G | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.3911+173T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243156048 | ||||||
| chr1:243156082
|
G | T | 1 | a0001c0001t0002g0095 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3911+139C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 14/19 | chr1 | 243156082 | ||||||
| chr1:243156547
|
G | A | 1 | a0002c0004t0001g0135 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3677-92C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243156547 | ||||||
| chr1:243156555
|
G | A | 1 | a0001c0007t0001g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3677-100C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243156555 | ||||||
| chr1:243156799
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3677-344G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243156799 | ||||||
| chr1:243156826
|
CA | C | 57 | a0001c0001t0001g0220a0001c0001t0002g0009a0001c0001t0002g0062others(54): Show | 57 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.3677-372delT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243156826 | ||||||
| chr1:243156895
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3677-440G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243156895 | ||||||
| chr1:243157050
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3677-595A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243157050 | ||||||
| chr1:243157289
|
T | G | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3677-834A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243157289 | ||||||
| chr1:243157307
|
A | G | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.3677-852T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243157307 | ||||||
| chr1:243157384
|
T | TA | 216 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(213): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.3677-930dupT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243157384 | ||||||
| chr1:243157428
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | NA18999.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.3677-973G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243157428 | ||||||
| chr1:243157808
|
C | T | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.3677-1353G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243157808 | ||||||
| chr1:243157923
|
A | G | 6 | a0001c0001t0002g0062a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG00738.hp2 HG02523.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3677-1468T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243157923 | ||||||
| chr1:243157992
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0073 | 2 | HG00099.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.3677-1537A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243157992 | ||||||
| chr1:243158228
|
A | G | 7 | a0001c0001t0002g0061a0001c0007t0001g0099a0001c0007t0001g0100others(4): Show | 7 | HG02145.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.3677-1773T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243158228 | ||||||
| chr1:243158673
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3677-2218G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243158673 | ||||||
| chr1:243158674
|
G | A | 3 | a0001c0001t0002g0009a0001c0001t0002g0095a0001c0001t0002g0126 | 3 | HG01106.hp1 HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3677-2219C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243158674 | ||||||
| chr1:243158825
|
T | C | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.3677-2370A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243158825 | ||||||
| chr1:243158899
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3677-2444A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243158899 | ||||||
| chr1:243158900
|
C | A | 1 | a0001c0014t0001g0110 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3677-2445G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243158900 | ||||||
| chr1:243159079
|
A | C | 68 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(65): Show | 68 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.3677-2624T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159079 | ||||||
| chr1:243159242
|
C | T | 56 | a0001c0001t0002g0009a0001c0001t0002g0062a0001c0001t0002g0081others(53): Show | 56 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.3677-2787G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159242 | ||||||
| chr1:243159310
|
C | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.3677-2855G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159310 | ||||||
| chr1:243159315
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3677-2860G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159315 | ||||||
| chr1:243159356
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3677-2901A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159356 | ||||||
| chr1:243159715
|
C | A | 2 | a0001c0001t0003g0123a0001c0001t0003g0124 | 2 | HG01109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3677-3260G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159715 | ||||||
| chr1:243159761
|
T | TTGTGTGT others(13): Show |
1 | a0001c0013t0001g0023 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3677-3307_3677-330 others(24): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159761 | ||||||
| chr1:243159761
|
T | TTGTGTGT others(17): Show |
1 | a0001c0001t0001g0026 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3677-3307_3677-330 others(28): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159761 | ||||||
| chr1:243159763
|
T | G | 2 | a0001c0001t0001g0026a0001c0013t0001g0023 | 2 | HG02074.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.3677-3308A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
T | TGTGTGTG others(6): Show |
1 | a0001c0001t0002g0255 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3677-3309_3677-330 others(17): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
T | TGTGTGTG others(12): Show |
1 | a0001c0001t0001g0078 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3677-3309_3677-330 others(23): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
T | TTG | 21 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0140others(18): Show | 21 | HG00735.hp1 HG01109.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.3677-3310_3677-330 others(6): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
T | TTGTG | 11 | a0001c0001t0001g0160a0001c0001t0002g0061a0001c0007t0001g0100others(8): Show | 11 | HG02145.hp2 HG02280.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.3677-3312_3677-330 others(8): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
T | TTGTGTG | 29 | a0001c0001t0001g0063a0001c0001t0001g0116a0001c0001t0001g0159others(26): Show | 30 | HG00140.hp1 HG00408.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.3677-3314_3677-330 others(10): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
T | TTGTGTGT others(1): Show |
8 | a0001c0001t0001g0032a0001c0001t0001g0087a0001c0001t0001g0088others(5): Show | 8 | HG01071.hp1 HG01175.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.3677-3316_3677-330 others(12): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
T | TTGTGTGT others(3): Show |
10 | a0001c0001t0001g0115a0001c0001t0002g0205a0003c0003t0003g0103others(7): Show | 10 | HG01884.hp2 HG02083.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.3677-3318_3677-330 others(14): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
T | TTGTGTGT others(5): Show |
13 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 13 | HG00738.hp2 HG02258.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.3677-3320_3677-330 others(16): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
T | TTGTGTGT others(7): Show |
8 | a0001c0001t0001g0027a0001c0001t0002g0081a0001c0001t0002g0186others(5): Show | 8 | HG00558.hp1 HG02965.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.3677-3322_3677-330 others(18): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
T | TTGTGTGT others(9): Show |
11 | a0001c0001t0001g0053a0001c0001t0001g0097a0001c0001t0001g0098others(8): Show | 11 | HG01106.hp1 HG02129.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.3677-3324_3677-330 others(20): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
T | TTGTGTGT others(11): Show |
12 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0049others(9): Show | 12 | HG02630.hp1 HG02717.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.3677-3326_3677-330 others(22): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
T | TTGTGTGT others(13): Show |
16 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0033others(13): Show | 16 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(13): Show |
intron_variant | MODIFIER | c.3677-3328_3677-330 others(24): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
T | TTGTGTGT others(15): Show |
7 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0051others(4): Show | 7 | HG01168.hp2 HG01169.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.3677-3330_3677-330 others(26): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
T | TTGTGTGT others(17): Show |
28 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(25): Show | 28 | HG00733.hp1 HG00741.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.3677-3332_3677-330 others(28): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
T | TTGTGTGT others(19): Show |
12 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0020others(9): Show | 13 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(10): Show |
intron_variant | MODIFIER | c.3677-3334_3677-330 others(30): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
T | TTGTGTGT others(21): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0045 | 3 | NA18994.hp1 NA18999.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.3677-3336_3677-330 others(32): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
T | TTGTGTGT others(23): Show |
5 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0052others(2): Show | 5 | HG00597.hp2 HG01099.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.3677-3338_3677-330 others(34): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
T | TTGTGTGT others(25): Show |
5 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0055others(2): Show | 5 | HG00099.hp2 HG02818.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3677-3340_3677-330 others(36): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
T | TTGTGTGT others(27): Show |
2 | a0001c0001t0001g0076a0001c0001t0001g0084 | 2 | HG01123.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.3677-3342_3677-330 others(38): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
TTG | T | 4 | a0001c0001t0001g0211a0001c0001t0001g0231a0001c0001t0001g0250others(1): Show | 4 | HG00423.hp2 NA18982.hp2 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.3677-3310_3677-330 others(6): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
TTGTG | T | 13 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189others(10): Show | 13 | HG01975.hp2 HG01978.hp2 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.3677-3312_3677-330 others(8): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159763
|
TTGTGTGT others(3): Show |
T | 1 | a0004c0005t0001g0198 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3677-3318_3677-330 others(14): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159763 | ||||||
| chr1:243159802
|
T | TGTGTGTG others(16): Show |
1 | a0001c0001t0001g0067 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3677-3348_3677-334 others(27): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159802 | ||||||
| chr1:243159802
|
T | TGTGTGTG others(20): Show |
1 | a0001c0001t0001g0073 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3677-3348_3677-334 others(31): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159802 | ||||||
| chr1:243159933
|
C | G | 1 | a0002c0002t0001g0165 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3677-3478G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243159933 | ||||||
| chr1:243160009
|
G | A | 3 | a0001c0001t0002g0186a0001c0001t0002g0269a0001c0001t0011g0295 | 3 | HG00558.hp1 NA18951.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.3677-3554C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243160009 | ||||||
| chr1:243160075
|
C | T | 14 | a0003c0003t0003g0103a0003c0003t0003g0107a0003c0003t0003g0149others(11): Show | 14 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.3677-3620G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243160075 | ||||||
| chr1:243160156
|
G | A | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3677-3701C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243160156 | ||||||
| chr1:243160204
|
C | T | 11 | a0003c0003t0003g0103a0003c0003t0003g0149a0003c0003t0003g0150others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.3677-3749G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243160204 | ||||||
| chr1:243160211
|
T | C | 3 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0066 | 3 | HG01099.hp1 HG01261.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3677-3756A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243160211 | ||||||
| chr1:243160515
|
C | G | 3 | a0001c0001t0003g0112a0001c0001t0003g0123a0001c0001t0003g0124 | 3 | HG01109.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3676+3769G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243160515 | ||||||
| chr1:243160550
|
T | C | 4 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(1): Show | 4 | HG02818.hp2 HG03041.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3676+3734A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243160550 | ||||||
| chr1:243160866
|
C | A | 207 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(204): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.3676+3418G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243160866 | ||||||
| chr1:243160919
|
TAAAAC | T | 42 | a0001c0001t0002g0009a0001c0001t0002g0062a0001c0001t0002g0081others(39): Show | 42 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.3676+3360_3676+336 others(9): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243160919 | ||||||
| chr1:243161056
|
C | T | 12 | a0001c0007t0001g0100a0002c0004t0001g0127a0002c0004t0001g0128others(9): Show | 12 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.3676+3228G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243161056 | ||||||
| chr1:243161102
|
C | A | 213 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(210): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.3676+3182G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243161102 | ||||||
| chr1:243161271
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3676+3013G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243161271 | ||||||
| chr1:243161303
|
C | CA | 95 | a0001c0001t0001g0070a0001c0001t0001g0115a0001c0001t0001g0116others(92): Show | 96 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.3676+2980dupT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243161303 | ||||||
| chr1:243161562
|
T | C | 14 | a0003c0003t0003g0103a0003c0003t0003g0107a0003c0003t0003g0149others(11): Show | 14 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.3676+2722A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243161562 | ||||||
| chr1:243162064
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3676+2220T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243162064 | ||||||
| chr1:243162141
|
A | G | 1 | a0001c0001t0005g0064 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3676+2143T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243162141 | ||||||
| chr1:243162248
|
A | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.3676+2036T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243162248 | ||||||
| chr1:243162632
|
T | C | 1 | a0001c0001t0001g0008 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3676+1652A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243162632 | ||||||
| chr1:243162947
|
A | T | 7 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(4): Show | 7 | HG01891.hp2 HG01981.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.3676+1337T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243162947 | ||||||
| chr1:243162958
|
G | A | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.3676+1326C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243162958 | ||||||
| chr1:243163055
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3676+1229A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243163055 | ||||||
| chr1:243163076
|
A | G | 63 | a0001c0001t0001g0106a0001c0001t0002g0009a0001c0001t0002g0061others(60): Show | 63 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.3676+1208T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243163076 | ||||||
| chr1:243163109
|
A | C | 59 | a0001c0001t0002g0009a0001c0001t0002g0061a0001c0001t0002g0062others(56): Show | 59 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.3676+1175T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243163109 | ||||||
| chr1:243163110
|
G | C | 59 | a0001c0001t0002g0009a0001c0001t0002g0061a0001c0001t0002g0062others(56): Show | 59 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.3676+1174C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243163110 | ||||||
| chr1:243163194
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3676+1090T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243163194 | ||||||
| chr1:243163528
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3676+756A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243163528 | ||||||
| chr1:243163696
|
A | T | 1 | a0001c0001t0001g0251 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3676+588T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243163696 | ||||||
| chr1:243163715
|
C | T | 1 | a0002c0021t0001g0174 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3676+569G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243163715 | ||||||
| chr1:243163729
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3676+555T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243163729 | ||||||
| chr1:243163970
|
A | G | 7 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0025others(4): Show | 7 | HG00438.hp1 HG00597.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.3676+314T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243163970 | ||||||
| chr1:243164088
|
T | C | 3 | a0001c0001t0003g0112a0001c0001t0003g0123a0001c0001t0003g0124 | 3 | HG01109.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3676+196A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243164088 | ||||||
| chr1:243164216
|
T | A | 8 | a0001c0001t0001g0106a0001c0001t0001g0115a0001c0001t0001g0116others(5): Show | 8 | HG01891.hp2 HG01981.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.3676+68A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243164216 | ||||||
| chr1:243164216
|
T | TA | 55 | a0001c0001t0002g0061a0001c0001t0002g0081a0001c0001t0002g0082others(52): Show | 55 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.3676+67_3676+68ins others(1): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243164216 | ||||||
| chr1:243164217
|
T | A | 67 | a0001c0001t0001g0106a0001c0001t0001g0115a0001c0001t0001g0116others(64): Show | 67 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.3676+67A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243164217 | ||||||
| chr1:243164217
|
TA | T | 10 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055others(7): Show | 10 | HG00639.hp1 HG02818.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.3676+66delT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243164217 | ||||||
| chr1:243164218
|
A | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(80): Show | 84 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.3676+66T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243164218 | ||||||
| chr1:243164219
|
A | T | 7 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 7 | HG02155.hp1 HG02818.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.3676+65T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 13/19 | chr1 | 243164219 | ||||||
| chr1:243166140
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1844-24T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243166140 | ||||||
| chr1:243166233
|
C | T | 1 | a0003c0003t0003g0107 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1844-117G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243166233 | ||||||
| chr1:243166274
|
T | C | 69 | a0001c0001t0001g0106a0001c0001t0001g0115a0001c0001t0001g0116others(66): Show | 69 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.1844-158A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243166274 | ||||||
| chr1:243166293
|
T | C | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1844-177A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243166293 | ||||||
| chr1:243166447
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(2): Show | 6 | HG00140.hp2 HG00280.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1844-331G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243166447 | ||||||
| chr1:243166577
|
T | TAAAAATG others(315): Show |
1 | a0001c0001t0001g0279 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1844-462_1844-461i others(324): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243166577 | ||||||
| chr1:243166694
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1844-578C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243166694 | ||||||
| chr1:243166735
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1844-619A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243166735 | ||||||
| chr1:243166852
|
C | T | 1 | a0001c0001t0001g0282 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1844-736G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243166852 | ||||||
| chr1:243167324
|
A | G | 3 | a0001c0001t0003g0112a0001c0001t0003g0123a0001c0001t0003g0124 | 3 | HG01109.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1844-1208T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243167324 | ||||||
| chr1:243168068
|
T | A | 4 | a0002c0004t0001g0132a0002c0004t0001g0135a0002c0004t0001g0136others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1843+1560A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243168068 | ||||||
| chr1:243168147
|
ACT | A | 23 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0188others(20): Show | 23 | HG00438.hp2 HG00558.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.1843+1479_1843+148 others(6): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243168147 | ||||||
| chr1:243168213
|
T | C | 59 | a0001c0001t0002g0009a0001c0001t0002g0061a0001c0001t0002g0062others(56): Show | 59 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.1843+1415A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243168213 | ||||||
| chr1:243168261
|
T | C | 7 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(4): Show | 7 | HG01891.hp2 HG01981.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1843+1367A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243168261 | ||||||
| chr1:243168382
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1843+1246A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243168382 | ||||||
| chr1:243168439
|
G | A | 59 | a0001c0001t0002g0009a0001c0001t0002g0061a0001c0001t0002g0062others(56): Show | 59 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.1843+1189C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243168439 | ||||||
| chr1:243168463
|
T | C | 59 | a0001c0001t0002g0009a0001c0001t0002g0061a0001c0001t0002g0062others(56): Show | 59 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.1843+1165A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243168463 | ||||||
| chr1:243168522
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1843+1106C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243168522 | ||||||
| chr1:243168567
|
G | A | 1 | a0001c0001t0002g0218 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1843+1061C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243168567 | ||||||
| chr1:243168756
|
G | T | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1843+872C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243168756 | ||||||
| chr1:243168803
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1843+825C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243168803 | ||||||
| chr1:243168993
|
TTA | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1843+633_1843+634d others(4): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243168993 | ||||||
| chr1:243169131
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1843+497T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243169131 | ||||||
| chr1:243169316
|
C | T | 2 | a0002c0004t0001g0132a0002c0004t0012g0296 | 2 | HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1843+312G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243169316 | ||||||
| chr1:243169317
|
G | A | 7 | a0002c0002t0001g0165a0002c0002t0001g0167a0002c0002t0001g0168others(4): Show | 7 | HG00408.hp1 HG00423.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.1843+311C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243169317 | ||||||
| chr1:243169339
|
A | G | 7 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(4): Show | 7 | HG01891.hp2 HG01981.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1843+289T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243169339 | ||||||
| chr1:243169535
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG00558.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1843+93A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243169535 | ||||||
| chr1:243169582
|
AAG | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(83): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.1843+44_1843+45del others(2): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 12/19 | chr1 | 243169582 | ||||||
| chr1:243169847
|
T | C | 1 | a0003c0003t0003g0107 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1717-93A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/19 | chr1 | 243169847 | ||||||
| chr1:243169871
|
C | T | 2 | a0002c0002t0001g0185a0002c0018t0001g0122 | 2 | HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1717-117G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/19 | chr1 | 243169871 | ||||||
| chr1:243170230
|
A | AC | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(254): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1717-477_1717-476i others(3): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/19 | chr1 | 243170230 | ||||||
| chr1:243170340
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1717-586C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/19 | chr1 | 243170340 | ||||||
| chr1:243170622
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1717-868G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/19 | chr1 | 243170622 | ||||||
| chr1:243170872
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1717-1118A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/19 | chr1 | 243170872 | ||||||
| chr1:243171083
|
C | T | 1 | a0002c0002t0001g0179 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1717-1329G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/19 | chr1 | 243171083 | ||||||
| chr1:243171085
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1717-1331A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/19 | chr1 | 243171085 | ||||||
| chr1:243171209
|
T | G | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1717-1455A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/19 | chr1 | 243171209 | ||||||
| chr1:243171588
|
T | C | 45 | a0001c0001t0002g0009a0001c0001t0002g0061a0001c0001t0002g0062others(42): Show | 45 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1716+1109A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/19 | chr1 | 243171588 | ||||||
| chr1:243171648
|
T | C | 3 | a0001c0007t0001g0099a0001c0007t0001g0100a0002c0019t0001g0131 | 3 | HG02486.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1716+1049A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/19 | chr1 | 243171648 | ||||||
| chr1:243171974
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(2): Show | 6 | HG00140.hp2 HG00280.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1716+723C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/19 | chr1 | 243171974 | ||||||
| chr1:243172023
|
G | A | 3 | a0001c0001t0003g0112a0001c0001t0003g0123a0001c0001t0003g0124 | 3 | HG01109.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1716+674C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/19 | chr1 | 243172023 | ||||||
| chr1:243172152
|
A | T | 1 | a0002c0021t0001g0174 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1716+545T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/19 | chr1 | 243172152 | ||||||
| chr1:243172203
|
C | G | 3 | a0002c0002t0001g0003a0002c0002t0001g0183a0002c0002t0001g0184 | 4 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1716+494G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/19 | chr1 | 243172203 | ||||||
| chr1:243172241
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1716+456G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/19 | chr1 | 243172241 | ||||||
| chr1:243172299
|
A | C | 1 | a0001c0001t0001g0272 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1716+398T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/19 | chr1 | 243172299 | ||||||
| chr1:243172342
|
A | G | 45 | a0001c0001t0002g0009a0001c0001t0002g0061a0001c0001t0002g0062others(42): Show | 45 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1716+355T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/19 | chr1 | 243172342 | ||||||
| chr1:243172638
|
GA | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(76): Show | 84 | HG00280.hp2 HG00423.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1716+58delT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 11/19 | chr1 | 243172638 | ||||||
| chr1:243172858
|
A | C | 7 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(4): Show | 7 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1567-12T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243172858 | ||||||
| chr1:243172988
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1567-142G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243172988 | ||||||
| chr1:243173082
|
C | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.1567-236G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243173082 | ||||||
| chr1:243173130
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0264 | 2 | HG01496.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1567-284C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243173130 | ||||||
| chr1:243173137
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1567-291G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243173137 | ||||||
| chr1:243173253
|
T | A | 10 | a0002c0002t0001g0163a0002c0002t0001g0164a0002c0002t0001g0166others(7): Show | 10 | HG00140.hp1 HG01192.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.1567-407A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243173253 | ||||||
| chr1:243173612
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1567-766A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243173612 | ||||||
| chr1:243173735
|
C | CA | 51 | a0001c0001t0001g0146a0001c0001t0001g0260a0001c0001t0002g0009others(48): Show | 51 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.1567-890dupT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243173735 | ||||||
| chr1:243173735
|
C | CAA | 8 | a0003c0003t0003g0149a0003c0003t0003g0150a0003c0003t0003g0152others(5): Show | 8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1567-891_1567-890d others(4): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243173735 | ||||||
| chr1:243173805
|
A | G | 1 | a0012c0022t0001g0259 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1567-959T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243173805 | ||||||
| chr1:243174059
|
A | T | 6 | a0001c0001t0002g0062a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG00738.hp2 HG02523.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1567-1213T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243174059 | ||||||
| chr1:243174071
|
G | GATT | 15 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(12): Show | 15 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1567-1228_1567-122 others(7): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243174071 | ||||||
| chr1:243174116
|
A | G | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1567-1270T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243174116 | ||||||
| chr1:243174179
|
T | TA | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1567-1334dupT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243174179 | ||||||
| chr1:243174283
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1567-1437C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243174283 | ||||||
| chr1:243174293
|
T | G | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1567-1447A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243174293 | ||||||
| chr1:243174330
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1567-1484T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243174330 | ||||||
| chr1:243174503
|
T | G | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1567-1657A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243174503 | ||||||
| chr1:243174733
|
T | C | 2 | a0003c0009t0003g0108a0003c0009t0003g0109 | 2 | HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1567-1887A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243174733 | ||||||
| chr1:243174782
|
G | A | 1 | a0001c0001t0008g0104 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1567-1936C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243174782 | ||||||
| chr1:243174782
|
GTTAAGT | G | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1567-1942_1567-193 others(10): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243174782 | ||||||
| chr1:243174814
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1567-1968T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243174814 | ||||||
| chr1:243174838
|
C | A | 1 | a0001c0001t0001g0251 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1567-1992G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243174838 | ||||||
| chr1:243174914
|
A | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.1567-2068T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243174914 | ||||||
| chr1:243175243
|
C | A | 22 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(19): Show | 22 | HG01109.hp1 HG01884.hp2 HG01981.hp1 others(19): Show |
intron_variant | MODIFIER | c.1567-2397G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243175243 | ||||||
| chr1:243175411
|
G | A | 1 | a0001c0001t0005g0064 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1567-2565C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243175411 | ||||||
| chr1:243175649
|
G | T | 1 | a0005c0006t0001g0233 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1567-2803C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243175649 | ||||||
| chr1:243175746
|
T | C | 1 | a0001c0001t0002g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1567-2900A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243175746 | ||||||
| chr1:243175778
|
T | C | 14 | a0003c0003t0003g0103a0003c0003t0003g0107a0003c0003t0003g0149others(11): Show | 14 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1567-2932A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243175778 | ||||||
| chr1:243175805
|
GT | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.1567-2960delA | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243175805 | ||||||
| chr1:243175842
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1567-2996C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243175842 | ||||||
| chr1:243175866
|
G | A | 44 | a0001c0001t0001g0220a0001c0001t0002g0009a0001c0001t0002g0062others(41): Show | 44 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1567-3020C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243175866 | ||||||
| chr1:243176018
|
C | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0237a0001c0001t0001g0280 | 4 | HG02735.hp1 HG03017.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1567-3172G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243176018 | ||||||
| chr1:243176030
|
T | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0237a0001c0001t0001g0280 | 4 | HG02735.hp1 HG03017.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1567-3184A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243176030 | ||||||
| chr1:243176034
|
C | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0237a0001c0001t0001g0280 | 4 | HG02735.hp1 HG03017.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1567-3188G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243176034 | ||||||
| chr1:243176039
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0237a0001c0001t0001g0280 | 4 | HG02735.hp1 HG03017.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1567-3193C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243176039 | ||||||
| chr1:243176490
|
C | CTATT | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(282): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1567-3645_1567-364 others(8): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243176490 | ||||||
| chr1:243177171
|
A | T | 14 | a0003c0003t0003g0103a0003c0003t0003g0107a0003c0003t0003g0149others(11): Show | 14 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1567-4325T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243177171 | ||||||
| chr1:243177215
|
G | A | 1 | a0002c0002t0001g0177 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1567-4369C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243177215 | ||||||
| chr1:243177256
|
A | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(80): Show | 88 | HG00280.hp2 HG00423.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1567-4410T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243177256 | ||||||
| chr1:243177320
|
T | G | 1 | a0007c0011t0001g0182 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1567-4474A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243177320 | ||||||
| chr1:243177702
|
T | A | 1 | a0002c0002t0001g0164 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1567-4856A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243177702 | ||||||
| chr1:243178076
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1567-5230G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243178076 | ||||||
| chr1:243178277
|
C | G | 1 | a0002c0004t0001g0129 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1567-5431G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243178277 | ||||||
| chr1:243178308
|
C | CA | 94 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 98 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1567-5463dupT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243178308 | ||||||
| chr1:243178308
|
C | CAA | 31 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0162others(28): Show | 32 | HG00423.hp1 HG00738.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1567-5464_1567-546 others(6): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243178308 | ||||||
| chr1:243178308
|
C | CAAA | 6 | a0001c0001t0001g0063a0001c0001t0001g0106a0001c0001t0001g0214others(3): Show | 6 | HG01175.hp2 HG01361.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1567-5465_1567-546 others(7): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243178308 | ||||||
| chr1:243178308
|
C | CAAAAAA | 18 | a0001c0001t0002g0009a0001c0001t0002g0082a0001c0001t0002g0092others(15): Show | 18 | HG00558.hp1 HG01106.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.1567-5468_1567-546 others(10): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243178308 | ||||||
| chr1:243178308
|
C | CAAAAAAA | 17 | a0001c0001t0002g0062a0001c0001t0002g0093a0001c0001t0002g0126others(14): Show | 17 | HG00438.hp2 HG00738.hp2 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.1567-5469_1567-546 others(11): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243178308 | ||||||
| chr1:243178308
|
C | CAAAAAAA others(3): Show |
3 | a0001c0001t0002g0274a0001c0001t0010g0215a0001c0015t0001g0223 | 3 | HG02056.hp1 NA18983.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1567-5472_1567-546 others(14): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243178308 | ||||||
| chr1:243178308
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0002g0081 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1567-5473_1567-546 others(15): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243178308 | ||||||
| chr1:243178308
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1567-5478_1567-546 others(20): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243178308 | ||||||
| chr1:243178308
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0002g0105 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1567-5478_1567-546 others(20): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243178308 | ||||||
| chr1:243178575
|
C | A | 1 | a0001c0001t0001g0272 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1567-5729G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243178575 | ||||||
| chr1:243178599
|
T | C | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1567-5753A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243178599 | ||||||
| chr1:243178821
|
C | T | 87 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(84): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.1567-5975G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243178821 | ||||||
| chr1:243178883
|
G | C | 1 | a0003c0003t0003g0107 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1567-6037C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243178883 | ||||||
| chr1:243178920
|
G | A | 1 | a0001c0001t0002g0105 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1567-6074C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243178920 | ||||||
| chr1:243179064
|
A | T | 1 | a0001c0001t0001g0148 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1567-6218T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243179064 | ||||||
| chr1:243179527
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1566+6252T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243179527 | ||||||
| chr1:243179613
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.1566+6166T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243179613 | ||||||
| chr1:243179920
|
C | T | 1 | a0005c0006t0001g0233 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1566+5859G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243179920 | ||||||
| chr1:243180000
|
A | G | 1 | a0001c0007t0001g0099 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1566+5779T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243180000 | ||||||
| chr1:243180026
|
C | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.1566+5753G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243180026 | ||||||
| chr1:243180705
|
G | T | 1 | a0001c0001t0002g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1566+5074C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243180705 | ||||||
| chr1:243180733
|
C | A | 2 | a0001c0001t0002g0062a0001c0001t0002g0082 | 2 | HG02523.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1566+5046G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243180733 | ||||||
| chr1:243180746
|
T | A | 1 | a0001c0001t0001g0106 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1566+5033A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243180746 | ||||||
| chr1:243180799
|
G | C | 67 | a0001c0001t0001g0106a0001c0001t0001g0115a0001c0001t0001g0116others(64): Show | 67 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.1566+4980C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243180799 | ||||||
| chr1:243180913
|
G | A | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1566+4866C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243180913 | ||||||
| chr1:243181269
|
T | A | 1 | a0001c0001t0001g0058 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1566+4510A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243181269 | ||||||
| chr1:243181430
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1566+4349T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243181430 | ||||||
| chr1:243181486
|
G | A | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0290others(1): Show | 4 | HG00741.hp1 HG01123.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1566+4293C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243181486 | ||||||
| chr1:243181734
|
T | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(2): Show | 6 | HG00140.hp2 HG00280.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1566+4045A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243181734 | ||||||
| chr1:243181798
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1566+3981A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243181798 | ||||||
| chr1:243182084
|
T | G | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1566+3695A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243182084 | ||||||
| chr1:243182106
|
T | C | 46 | a0001c0001t0002g0009a0001c0001t0002g0061a0001c0001t0002g0062others(43): Show | 46 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1566+3673A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243182106 | ||||||
| chr1:243182113
|
AT | A | 3 | a0001c0001t0003g0112a0001c0001t0003g0123a0001c0001t0003g0124 | 3 | HG01109.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1566+3665delA | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243182113 | ||||||
| chr1:243182689
|
CAT | C | 3 | a0001c0001t0003g0112a0001c0001t0003g0123a0001c0001t0003g0124 | 3 | HG01109.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1566+3088_1566+308 others(6): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243182689 | ||||||
| chr1:243182782
|
C | T | 2 | a0001c0001t0001g0026a0001c0013t0001g0023 | 2 | HG02074.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1566+2997G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243182782 | ||||||
| chr1:243182790
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1566+2989A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243182790 | ||||||
| chr1:243182967
|
A | T | 12 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(9): Show | 12 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1566+2812T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243182967 | ||||||
| chr1:243182971
|
C | CT | 11 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0016others(8): Show | 12 | HG00140.hp2 HG00280.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1566+2807dupA | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243182971 | ||||||
| chr1:243183046
|
C | T | 12 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(9): Show | 12 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1566+2733G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243183046 | ||||||
| chr1:243183102
|
T | C | 175 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1566+2677A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243183102 | ||||||
| chr1:243183200
|
C | T | 1 | a0002c0002t0001g0171 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1566+2579G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243183200 | ||||||
| chr1:243183269
|
C | T | 8 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0025others(5): Show | 8 | HG00438.hp1 HG00597.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.1566+2510G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243183269 | ||||||
| chr1:243183270
|
G | A | 1 | a0002c0002t0001g0169 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1566+2509C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243183270 | ||||||
| chr1:243183406
|
A | G | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1566+2373T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243183406 | ||||||
| chr1:243183477
|
G | A | 24 | a0002c0002t0001g0003a0002c0002t0001g0163a0002c0002t0001g0164others(21): Show | 25 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.1566+2302C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243183477 | ||||||
| chr1:243183777
|
T | A | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1566+2002A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243183777 | ||||||
| chr1:243183849
|
T | A | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(1): Show | 4 | HG01071.hp1 HG01175.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1566+1930A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243183849 | ||||||
| chr1:243184289
|
A | C | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1566+1490T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243184289 | ||||||
| chr1:243184360
|
C | A | 3 | a0002c0002t0001g0171a0002c0002t0001g0178a0007c0011t0001g0182 | 3 | HG01993.hp2 HG03942.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1566+1419G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243184360 | ||||||
| chr1:243184362
|
C | A | 64 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0033others(61): Show | 65 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.1566+1417G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243184362 | ||||||
| chr1:243184364
|
A | C | 12 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(9): Show | 12 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.1566+1415T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243184364 | ||||||
| chr1:243184573
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1566+1206T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243184573 | ||||||
| chr1:243184621
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1566+1158C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243184621 | ||||||
| chr1:243184912
|
T | A | 1 | a0001c0001t0001g0278 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1566+867A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243184912 | ||||||
| chr1:243184969
|
G | A | 6 | a0001c0001t0002g0061a0001c0007t0001g0099a0001c0007t0001g0100others(3): Show | 6 | HG02145.hp2 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1566+810C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243184969 | ||||||
| chr1:243185000
|
G | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0097others(2): Show | 5 | HG02451.hp1 HG02922.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1566+779C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243185000 | ||||||
| chr1:243185283
|
T | C | 1 | a0001c0014t0001g0110 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1566+496A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243185283 | ||||||
| chr1:243185315
|
C | T | 1 | a0002c0002t0001g0175 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1566+464G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243185315 | ||||||
| chr1:243185426
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1566+353C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243185426 | ||||||
| chr1:243185552
|
A | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(73): Show | 81 | HG00280.hp2 HG00423.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.1566+227T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243185552 | ||||||
| chr1:243185632
|
T | C | 1 | a0001c0001t0001g0029 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1566+147A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243185632 | ||||||
| chr1:243185643
|
G | A | 1 | a0001c0001t0008g0104 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1566+136C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 10/19 | chr1 | 243185643 | ||||||
| chr1:243186613
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1109-191T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243186613 | ||||||
| chr1:243186715
|
C | T | 1 | a0003c0003t0003g0107 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1109-293G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243186715 | ||||||
| chr1:243186909
|
A | C | 1 | a0003c0003t0003g0107 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1109-487T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243186909 | ||||||
| chr1:243186997
|
A | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0106 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1109-575T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243186997 | ||||||
| chr1:243187497
|
T | C | 1 | a0003c0003t0003g0107 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1109-1075A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243187497 | ||||||
| chr1:243187554
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1109-1132G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243187554 | ||||||
| chr1:243187723
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1109-1301A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243187723 | ||||||
| chr1:243187764
|
C | G | 4 | a0001c0001t0001g0059a0001c0001t0001g0067a0001c0001t0001g0068others(1): Show | 4 | HG00609.hp2 NA19007.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.1109-1342G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243187764 | ||||||
| chr1:243187820
|
C | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0106 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1109-1398G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243187820 | ||||||
| chr1:243188105
|
C | A | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(287): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1109-1683G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243188105 | ||||||
| chr1:243188301
|
T | C | 1 | a0001c0001t0001g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1109-1879A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243188301 | ||||||
| chr1:243188329
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1109-1907A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243188329 | ||||||
| chr1:243188614
|
A | T | 58 | a0001c0001t0002g0009a0001c0001t0002g0061a0001c0001t0002g0062others(55): Show | 58 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.1109-2192T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243188614 | ||||||
| chr1:243188924
|
A | T | 1 | a0002c0018t0001g0122 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1108+2094T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243188924 | ||||||
| chr1:243188947
|
T | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0052 | 2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1108+2071A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243188947 | ||||||
| chr1:243188979
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1108+2039A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243188979 | ||||||
| chr1:243188982
|
T | C | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG02735.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1108+2036A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243188982 | ||||||
| chr1:243189273
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1108+1745G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243189273 | ||||||
| chr1:243189282
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1108+1736G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243189282 | ||||||
| chr1:243189353
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1108+1665T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243189353 | ||||||
| chr1:243189438
|
T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.1108+1580A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243189438 | ||||||
| chr1:243189512
|
C | T | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1108+1506G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243189512 | ||||||
| chr1:243189556
|
C | CA | 12 | a0001c0001t0001g0018a0001c0001t0001g0027a0001c0001t0001g0050others(9): Show | 12 | HG01099.hp1 HG01192.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1108+1461dupT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243189556 | ||||||
| chr1:243189574
|
AT | A | 3 | a0001c0001t0003g0112a0001c0001t0003g0123a0001c0001t0003g0124 | 3 | HG01109.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1108+1443delA | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243189574 | ||||||
| chr1:243189575
|
T | A | 1 | a0002c0002t0001g0177 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1108+1443A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243189575 | ||||||
| chr1:243189845
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1108+1173G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243189845 | ||||||
| chr1:243189883
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1108+1135T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243189883 | ||||||
| chr1:243189913
|
G | A | 1 | a0003c0003t0003g0107 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1108+1105C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243189913 | ||||||
| chr1:243189913
|
G | C | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1108+1105C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243189913 | ||||||
| chr1:243190240
|
C | A | 1 | a0003c0003t0003g0161 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1108+778G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243190240 | ||||||
| chr1:243190287
|
C | T | 2 | a0001c0001t0003g0123a0001c0001t0003g0124 | 2 | HG01109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1108+731G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243190287 | ||||||
| chr1:243190567
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1108+451T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243190567 | ||||||
| chr1:243190590
|
T | C | 69 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0111others(66): Show | 69 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.1108+428A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243190590 | ||||||
| chr1:243190666
|
T | C | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1108+352A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243190666 | ||||||
| chr1:243190730
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(279): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1108+288T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243190730 | ||||||
| chr1:243190869
|
A | G | 7 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(4): Show | 7 | HG01891.hp2 HG01981.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1108+149T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243190869 | ||||||
| chr1:243190872
|
T | C | 2 | a0002c0002t0001g0163a0002c0002t0001g0180 | 2 | HG00140.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1108+146A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243190872 | ||||||
| chr1:243190951
|
C | A | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1108+67G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 8/19 | chr1 | 243190951 | ||||||
| chr1:243191677
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.632-183G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243191677 | ||||||
| chr1:243191902
|
G | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(79): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.632-408C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243191902 | ||||||
| chr1:243192039
|
C | T | 2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | NA18964.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.632-545G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243192039 | ||||||
| chr1:243192165
|
C | T | 63 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0111others(60): Show | 63 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.632-671G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243192165 | ||||||
| chr1:243192203
|
A | G | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.632-709T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243192203 | ||||||
| chr1:243192309
|
G | A | 11 | a0003c0003t0003g0103a0003c0003t0003g0149a0003c0003t0003g0150others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.632-815C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243192309 | ||||||
| chr1:243192470
|
T | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(83): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.632-976A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243192470 | ||||||
| chr1:243192494
|
G | A | 2 | a0001c0007t0001g0099a0001c0007t0001g0100 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.632-1000C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243192494 | ||||||
| chr1:243192671
|
C | T | 3 | a0001c0001t0003g0112a0001c0001t0003g0123a0001c0001t0003g0124 | 3 | HG01109.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.632-1177G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243192671 | ||||||
| chr1:243192885
|
T | C | 3 | a0001c0001t0001g0162a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG01891.hp1 HG02257.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.632-1391A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243192885 | ||||||
| chr1:243193032
|
G | A | 1 | a0001c0014t0001g0110 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.632-1538C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243193032 | ||||||
| chr1:243193155
|
TGTGA | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0243a0001c0001t0001g0260others(1): Show | 5 | HG02809.hp1 NA18946.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.632-1665_632-1662d others(6): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243193155 | ||||||
| chr1:243193299
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0271 | 2 | HG00408.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.632-1805C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243193299 | ||||||
| chr1:243193436
|
C | T | 3 | a0001c0001t0003g0112a0001c0001t0003g0123a0001c0001t0003g0124 | 3 | HG01109.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.632-1942G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243193436 | ||||||
| chr1:243193477
|
A | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(85): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.632-1983T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243193477 | ||||||
| chr1:243193867
|
T | C | 1 | a0001c0007t0001g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.632-2373A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243193867 | ||||||
| chr1:243194087
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.632-2593G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243194087 | ||||||
| chr1:243194325
|
C | T | 1 | a0001c0001t0001g0284 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.632-2831G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243194325 | ||||||
| chr1:243194453
|
T | C | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.632-2959A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243194453 | ||||||
| chr1:243194476
|
GTAAT | G | 3 | a0001c0001t0003g0112a0001c0001t0003g0123a0001c0001t0003g0124 | 3 | HG01109.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.632-2986_632-2983d others(6): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243194476 | ||||||
| chr1:243194942
|
T | A | 1 | a0001c0001t0001g0203 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.632-3448A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243194942 | ||||||
| chr1:243195244
|
T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.632-3750A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243195244 | ||||||
| chr1:243195378
|
C | T | 67 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0111others(64): Show | 67 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.631+3682G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243195378 | ||||||
| chr1:243195517
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.631+3543C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243195517 | ||||||
| chr1:243195623
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(75): Show | 83 | HG00280.hp2 HG00423.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.631+3437A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243195623 | ||||||
| chr1:243195654
|
C | T | 1 | a0001c0001t0002g0105 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.631+3406G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243195654 | ||||||
| chr1:243195839
|
A | G | 9 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(6): Show | 9 | HG01109.hp1 HG01981.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.631+3221T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243195839 | ||||||
| chr1:243195959
|
C | T | 1 | a0001c0007t0001g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.631+3101G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243195959 | ||||||
| chr1:243196045
|
G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 89 | HG00280.hp2 HG00423.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.631+3015C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243196045 | ||||||
| chr1:243196057
|
A | G | 1 | a0002c0002t0003g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.631+3003T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243196057 | ||||||
| chr1:243196370
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.631+2690G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243196370 | ||||||
| chr1:243196379
|
C | T | 3 | a0001c0001t0001g0249a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | NA18979.hp1 NA18984.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.631+2681G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243196379 | ||||||
| chr1:243196460
|
C | A | 66 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0111others(63): Show | 66 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.631+2600G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243196460 | ||||||
| chr1:243196549
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.631+2511C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243196549 | ||||||
| chr1:243196738
|
G | A | 1 | a0001c0001t0003g0124 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.631+2322C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243196738 | ||||||
| chr1:243196936
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.631+2124C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243196936 | ||||||
| chr1:243197025
|
A | C | 1 | a0002c0002t0003g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.631+2035T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243197025 | ||||||
| chr1:243197141
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.631+1919A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243197141 | ||||||
| chr1:243197389
|
A | ACT | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(84): Show | 92 | HG00280.hp2 HG00423.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.631+1670_631+1671i others(4): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243197389 | ||||||
| chr1:243197635
|
G | C | 4 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(1): Show | 4 | HG02818.hp2 HG03041.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+1425C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243197635 | ||||||
| chr1:243197652
|
C | G | 84 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(81): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.631+1408G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243197652 | ||||||
| chr1:243198457
|
G | A | 3 | a0001c0001t0001g0278a0001c0001t0002g0009a0001c0001t0002g0095 | 3 | HG01106.hp1 HG02683.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.631+603C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243198457 | ||||||
| chr1:243198844
|
C | T | 24 | a0002c0002t0001g0003a0002c0002t0001g0163a0002c0002t0001g0164others(21): Show | 25 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.631+216G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243198844 | ||||||
| chr1:243198878
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.631+182A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243198878 | ||||||
| chr1:243198964
|
T | C | 1 | a0002c0002t0003g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.631+96A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243198964 | ||||||
| chr1:243199029
|
C | T | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(254): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.631+31G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 7/19 | chr1 | 243199029 | ||||||
| chr1:243199252
|
T | C | 6 | a0001c0001t0002g0062a0001c0001t0002g0081a0001c0001t0002g0082others(3): Show | 6 | HG00738.hp2 HG02523.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-58A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 6/19 | chr1 | 243199252 | ||||||
| chr1:243199333
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.497-139G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 6/19 | chr1 | 243199333 | ||||||
| chr1:243199378
|
A | G | 62 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0111others(59): Show | 62 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.497-184T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 6/19 | chr1 | 243199378 | ||||||
| chr1:243199606
|
T | C | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.497-412A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 6/19 | chr1 | 243199606 | ||||||
| chr1:243199682
|
C | A | 1 | a0001c0001t0001g0251 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.497-488G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 6/19 | chr1 | 243199682 | ||||||
| chr1:243199724
|
T | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.497-530A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 6/19 | chr1 | 243199724 | ||||||
| chr1:243199767
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.497-573G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 6/19 | chr1 | 243199767 | ||||||
| chr1:243200387
|
T | C | 3 | a0001c0001t0002g0061a0006c0008t0002g0101a0006c0008t0002g0102 | 3 | HG02145.hp2 HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.496+131A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 6/19 | chr1 | 243200387 | ||||||
| chr1:243200492
|
T | TG | 12 | a0001c0001t0001g0098a0003c0003t0003g0103a0003c0003t0003g0149others(9): Show | 12 | HG01884.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.496+25dupC | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 6/19 | chr1 | 243200492 | ||||||
| chr1:243200689
|
C | T | 7 | a0004c0005t0001g0192a0004c0005t0001g0193a0004c0005t0001g0196others(4): Show | 7 | HG00735.hp1 HG01109.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-9G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 5/19 | chr1 | 243200689 | ||||||
| chr1:243200995
|
G | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(83): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.275-160C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243200995 | ||||||
| chr1:243201312
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.275-477C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243201312 | ||||||
| chr1:243201313
|
C | A | 1 | a0001c0001t0001g0073 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.275-478G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243201313 | ||||||
| chr1:243201330
|
A | G | 3 | a0001c0001t0003g0112a0001c0001t0003g0123a0001c0001t0003g0124 | 3 | HG01109.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.275-495T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243201330 | ||||||
| chr1:243201615
|
G | A | 62 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0111others(59): Show | 62 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.275-780C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243201615 | ||||||
| chr1:243201644
|
T | A | 3 | a0001c0001t0003g0112a0001c0001t0003g0123a0001c0001t0003g0124 | 3 | HG01109.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.275-809A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243201644 | ||||||
| chr1:243201894
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(76): Show | 84 | HG00280.hp2 HG00423.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.275-1059A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243201894 | ||||||
| chr1:243202260
|
A | C | 1 | a0001c0001t0001g0031 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.275-1425T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243202260 | ||||||
| chr1:243202363
|
C | G | 12 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(9): Show | 12 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.275-1528G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243202363 | ||||||
| chr1:243202613
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.275-1778A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243202613 | ||||||
| chr1:243202885
|
C | T | 3 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0264 | 3 | HG00639.hp1 HG01496.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.275-2050G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243202885 | ||||||
| chr1:243202894
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.275-2059G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243202894 | ||||||
| chr1:243202927
|
T | C | 1 | a0001c0001t0001g0277 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.275-2092A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243202927 | ||||||
| chr1:243202973
|
C | T | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG02735.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.275-2138G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243202973 | ||||||
| chr1:243202976
|
G | C | 1 | a0001c0001t0001g0210 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.275-2141C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243202976 | ||||||
| chr1:243203453
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.275-2618T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243203453 | ||||||
| chr1:243203503
|
G | A | 24 | a0002c0002t0001g0003a0002c0002t0001g0163a0002c0002t0001g0164others(21): Show | 25 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.275-2668C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243203503 | ||||||
| chr1:243203628
|
C | T | 159 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(156): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.275-2793G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243203628 | ||||||
| chr1:243203670
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.275-2835T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243203670 | ||||||
| chr1:243203845
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.275-3010C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243203845 | ||||||
| chr1:243204257
|
T | C | 1 | a0003c0009t0003g0109 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.275-3422A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243204257 | ||||||
| chr1:243204316
|
G | C | 1 | a0001c0001t0001g0285 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.275-3481C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243204316 | ||||||
| chr1:243204439
|
T | C | 7 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0081others(4): Show | 7 | HG00738.hp2 HG02145.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.275-3604A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243204439 | ||||||
| chr1:243204440
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.275-3605A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243204440 | ||||||
| chr1:243205151
|
A | T | 1 | a0001c0001t0001g0074 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.275-4316T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243205151 | ||||||
| chr1:243205407
|
G | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(83): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.275-4572C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243205407 | ||||||
| chr1:243205451
|
T | C | 1 | a0001c0001t0002g0256 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-4616A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243205451 | ||||||
| chr1:243205460
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.275-4625T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243205460 | ||||||
| chr1:243205597
|
G | A | 1 | a0001c0014t0001g0110 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.275-4762C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243205597 | ||||||
| chr1:243205770
|
A | C | 9 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(6): Show | 9 | HG01109.hp1 HG01981.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.275-4935T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243205770 | ||||||
| chr1:243205928
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.275-5093T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243205928 | ||||||
| chr1:243205936
|
G | GAAGAAGA others(18): Show |
1 | a0001c0001t0001g0275 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.275-5126_275-5102d others(27): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243205936 | ||||||
| chr1:243206047
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.275-5212C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243206047 | ||||||
| chr1:243206213
|
A | C | 1 | a0002c0002t0001g0170 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.275-5378T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243206213 | ||||||
| chr1:243206381
|
CT | C | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(281): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.274+5504delA | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243206381 | ||||||
| chr1:243206423
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(279): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.274+5463T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243206423 | ||||||
| chr1:243206431
|
C | G | 60 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0111others(57): Show | 60 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.274+5455G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243206431 | ||||||
| chr1:243206626
|
C | T | 69 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0111others(66): Show | 69 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.274+5260G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243206626 | ||||||
| chr1:243206669
|
T | C | 1 | a0002c0002t0001g0164 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.274+5217A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243206669 | ||||||
| chr1:243206930
|
G | A | 2 | a0002c0002t0001g0168a0002c0002t0001g0179 | 2 | NA19000.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.274+4956C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243206930 | ||||||
| chr1:243207003
|
A | G | 158 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(155): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.274+4883T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243207003 | ||||||
| chr1:243207010
|
G | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(146): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.274+4876C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243207010 | ||||||
| chr1:243207474
|
G | A | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.274+4412C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243207474 | ||||||
| chr1:243207509
|
C | CTGAA | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.274+4373_274+4376d others(6): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243207509 | ||||||
| chr1:243207570
|
T | G | 1 | a0001c0001t0001g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274+4316A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243207570 | ||||||
| chr1:243207638
|
A | G | 3 | a0001c0001t0003g0112a0001c0001t0003g0123a0001c0001t0003g0124 | 3 | HG01109.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.274+4248T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243207638 | ||||||
| chr1:243207714
|
A | C | 2 | a0002c0002t0001g0185a0002c0018t0001g0122 | 2 | HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.274+4172T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243207714 | ||||||
| chr1:243207750
|
C | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(279): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.274+4136G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243207750 | ||||||
| chr1:243207849
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.274+4037T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243207849 | ||||||
| chr1:243208126
|
C | T | 1 | a0001c0014t0001g0110 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.274+3760G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243208126 | ||||||
| chr1:243208176
|
A | G | 1 | a0001c0001t0002g0270 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.274+3710T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243208176 | ||||||
| chr1:243208177
|
G | A | 1 | a0001c0001t0002g0270 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.274+3709C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243208177 | ||||||
| chr1:243208314
|
C | G | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.274+3572G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243208314 | ||||||
| chr1:243208344
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.274+3542T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243208344 | ||||||
| chr1:243208398
|
C | T | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.274+3488G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243208398 | ||||||
| chr1:243208459
|
T | C | 25 | a0001c0001t0001g0225a0002c0002t0001g0003a0002c0002t0001g0163others(22): Show | 26 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.274+3427A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243208459 | ||||||
| chr1:243208468
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.274+3418G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243208468 | ||||||
| chr1:243208855
|
TCA | T | 4 | a0001c0001t0003g0112a0001c0001t0003g0123a0001c0001t0003g0124others(1): Show | 4 | HG01109.hp1 HG02622.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+3029_274+3030d others(4): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243208855 | ||||||
| chr1:243208865
|
A | G | 1 | a0002c0019t0001g0131 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.274+3021T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243208865 | ||||||
| chr1:243208901
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(229): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.274+2985C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243208901 | ||||||
| chr1:243208952
|
C | A | 1 | a0001c0001t0001g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.274+2934G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243208952 | ||||||
| chr1:243209117
|
T | C | 1 | a0001c0001t0002g0081 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.274+2769A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243209117 | ||||||
| chr1:243209270
|
C | T | 2 | a0001c0007t0001g0099a0001c0007t0001g0100 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.274+2616G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243209270 | ||||||
| chr1:243209421
|
A | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(83): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.274+2465T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243209421 | ||||||
| chr1:243209442
|
C | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(79): Show | 87 | HG00280.hp2 HG00423.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.274+2444G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243209442 | ||||||
| chr1:243209476
|
T | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(236): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.274+2410A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243209476 | ||||||
| chr1:243209519
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.274+2367G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243209519 | ||||||
| chr1:243209633
|
A | G | 19 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(16): Show | 19 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.274+2253T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243209633 | ||||||
| chr1:243209673
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.274+2213G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243209673 | ||||||
| chr1:243209701
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.274+2185T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243209701 | ||||||
| chr1:243209829
|
A | G | 1 | a0001c0013t0001g0023 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.274+2057T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243209829 | ||||||
| chr1:243209973
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.274+1913T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243209973 | ||||||
| chr1:243210109
|
G | A | 1 | a0002c0002t0001g0180 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.274+1777C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243210109 | ||||||
| chr1:243210532
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.274+1354C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243210532 | ||||||
| chr1:243210608
|
A | AT | 87 | a0001c0001t0001g0106a0001c0001t0001g0141a0001c0001t0001g0143others(84): Show | 89 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.274+1277dupA | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243210608 | ||||||
| chr1:243210608
|
A | ATT | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(82): Show | 89 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.274+1276_274+1277d others(4): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243210608 | ||||||
| chr1:243210608
|
A | ATTT | 86 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(83): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.274+1275_274+1277d others(5): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243210608 | ||||||
| chr1:243210608
|
A | ATTTT | 15 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0018others(12): Show | 15 | HG00408.hp2 HG00741.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.274+1274_274+1277d others(6): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243210608 | ||||||
| chr1:243210608
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.274+1266_274+1277d others(14): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243210608 | ||||||
| chr1:243210609
|
T | TA | 3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0111 | 3 | HG02451.hp1 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.274+1276_274+1277i others(3): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243210609 | ||||||
| chr1:243210875
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(241): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.274+1011T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243210875 | ||||||
| chr1:243210922
|
C | T | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.274+964G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243210922 | ||||||
| chr1:243211108
|
C | CA | 27 | a0001c0001t0001g0059a0001c0001t0001g0281a0001c0001t0002g0187others(24): Show | 28 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.274+777dupT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243211108 | ||||||
| chr1:243211265
|
C | T | 60 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0111others(57): Show | 60 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.274+621G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243211265 | ||||||
| chr1:243211513
|
T | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(84): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.274+373A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243211513 | ||||||
| chr1:243211545
|
T | C | 47 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0111others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.274+341A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243211545 | ||||||
| chr1:243211596
|
T | C | 7 | a0002c0002t0001g0164a0002c0002t0001g0166a0002c0002t0001g0169others(4): Show | 7 | HG01928.hp2 HG01993.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.274+290A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 4/19 | chr1 | 243211596 | ||||||
| chr1:243212016
|
A | G | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-52T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243212016 | ||||||
| chr1:243212068
|
C | T | 1 | a0002c0002t0003g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.196-104G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243212068 | ||||||
| chr1:243212234
|
A | G | 3 | a0001c0001t0002g0061a0006c0008t0002g0101a0006c0008t0002g0102 | 3 | HG02145.hp2 HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.196-270T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243212234 | ||||||
| chr1:243212309
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.196-345G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243212309 | ||||||
| chr1:243212688
|
T | TTC | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(275): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.196-726_196-725dup others(2): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243212688 | ||||||
| chr1:243213052
|
C | T | 13 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(10): Show | 13 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.196-1088G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243213052 | ||||||
| chr1:243213169
|
G | A | 1 | a0001c0001t0008g0104 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.196-1205C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243213169 | ||||||
| chr1:243213177
|
C | T | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.196-1213G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243213177 | ||||||
| chr1:243213455
|
T | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 116 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.196-1491A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243213455 | ||||||
| chr1:243213518
|
T | C | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.196-1554A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243213518 | ||||||
| chr1:243213899
|
T | C | 23 | a0002c0002t0001g0003a0002c0002t0001g0163a0002c0002t0001g0164others(20): Show | 24 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.196-1935A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243213899 | ||||||
| chr1:243213917
|
C | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(252): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.196-1953G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243213917 | ||||||
| chr1:243214280
|
G | GT | 120 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(117): Show | 125 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.196-2317dupA | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243214280 | ||||||
| chr1:243214280
|
G | GTT | 29 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0106others(26): Show | 29 | HG01106.hp1 HG01884.hp2 HG02027.hp2 others(26): Show |
intron_variant | MODIFIER | c.196-2318_196-2317d others(4): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243214280 | ||||||
| chr1:243214280
|
GT | G | 8 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0001t0002g0093others(5): Show | 9 | HG00738.hp2 HG01243.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.196-2317delA | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243214280 | ||||||
| chr1:243214378
|
C | T | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.196-2414G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243214378 | ||||||
| chr1:243214386
|
A | C | 1 | a0001c0001t0002g0009 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.196-2422T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243214386 | ||||||
| chr1:243214389
|
G | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0066 | 3 | HG01099.hp1 HG01261.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.196-2425C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243214389 | ||||||
| chr1:243214405
|
C | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 117 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.196-2441G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243214405 | ||||||
| chr1:243214437
|
C | T | 9 | a0003c0003t0003g0149a0003c0003t0003g0150a0003c0003t0003g0151others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-2473G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243214437 | ||||||
| chr1:243214442
|
C | T | 3 | a0002c0004t0001g0132a0002c0004t0001g0136a0002c0004t0012g0296 | 3 | HG02559.hp1 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.196-2478G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243214442 | ||||||
| chr1:243214474
|
T | G | 1 | a0001c0001t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.196-2510A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243214474 | ||||||
| chr1:243214578
|
G | GCCCAGCC others(319): Show |
1 | a0002c0002t0001g0164 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.196-2615_196-2614i others(328): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243214578 | ||||||
| chr1:243214578
|
G | GCCCAGCC others(320): Show |
18 | a0002c0002t0001g0003a0002c0002t0001g0163a0002c0002t0001g0165others(15): Show | 19 | HG00140.hp1 HG00408.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.196-2615_196-2614i others(329): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243214578 | ||||||
| chr1:243214578
|
G | GCCCAGCC others(321): Show |
3 | a0002c0002t0001g0168a0002c0002t0001g0173a0002c0021t0001g0174 | 3 | HG00423.hp2 NA18946.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.196-2615_196-2614i others(330): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243214578 | ||||||
| chr1:243214578
|
G | GCCCAGCC others(322): Show |
1 | a0002c0002t0001g0177 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.196-2615_196-2614i others(331): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243214578 | ||||||
| chr1:243214590
|
T | A | 113 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 118 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.196-2626A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243214590 | ||||||
| chr1:243214617
|
C | T | 3 | a0001c0001t0003g0123a0001c0001t0003g0124a0002c0018t0001g0122 | 3 | HG01109.hp1 HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.196-2653G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243214617 | ||||||
| chr1:243214845
|
T | C | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-2881A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243214845 | ||||||
| chr1:243215104
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.196-3140A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243215104 | ||||||
| chr1:243215294
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG00639.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.196-3330C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243215294 | ||||||
| chr1:243215397
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.196-3433G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243215397 | ||||||
| chr1:243215535
|
G | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0065a0002c0004t0001g0135 | 3 | HG02647.hp1 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.196-3571C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243215535 | ||||||
| chr1:243215616
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 116 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.196-3652C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243215616 | ||||||
| chr1:243215638
|
A | G | 27 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0106others(24): Show | 27 | HG01106.hp1 HG01884.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.196-3674T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243215638 | ||||||
| chr1:243215685
|
A | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(94): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.196-3721T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243215685 | ||||||
| chr1:243215834
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(241): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.196-3870T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243215834 | ||||||
| chr1:243215840
|
C | G | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(253): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.196-3876G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243215840 | ||||||
| chr1:243215844
|
G | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | HG00741.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.196-3880C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243215844 | ||||||
| chr1:243215864
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.196-3900C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243215864 | ||||||
| chr1:243215922
|
T | C | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.196-3958A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243215922 | ||||||
| chr1:243216172
|
T | G | 1 | a0001c0001t0001g0258 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.196-4208A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243216172 | ||||||
| chr1:243216218
|
A | T | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.196-4254T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243216218 | ||||||
| chr1:243216221
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.196-4257G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243216221 | ||||||
| chr1:243216265
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.196-4301T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243216265 | ||||||
| chr1:243216309
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.196-4345C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243216309 | ||||||
| chr1:243216352
|
C | A | 1 | a0001c0001t0001g0022 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.196-4388G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243216352 | ||||||
| chr1:243216367
|
A | G | 3 | a0002c0002t0001g0003a0002c0002t0001g0183a0002c0002t0001g0184 | 4 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-4403T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243216367 | ||||||
| chr1:243216410
|
T | C | 1 | a0001c0001t0002g0226 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.196-4446A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243216410 | ||||||
| chr1:243216561
|
C | G | 4 | a0001c0001t0001g0059a0001c0001t0001g0067a0001c0001t0001g0068others(1): Show | 4 | HG00609.hp2 NA19007.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-4597G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243216561 | ||||||
| chr1:243216601
|
A | T | 26 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0106others(23): Show | 26 | HG01106.hp1 HG01884.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.196-4637T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243216601 | ||||||
| chr1:243217067
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.195+4657A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243217067 | ||||||
| chr1:243217070
|
T | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(7): Show | 11 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(8): Show |
intron_variant | MODIFIER | c.195+4654A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243217070 | ||||||
| chr1:243217074
|
G | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 116 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.195+4650C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243217074 | ||||||
| chr1:243217180
|
G | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.195+4544C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243217180 | ||||||
| chr1:243217211
|
A | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(101): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.195+4513T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243217211 | ||||||
| chr1:243217867
|
A | C | 1 | a0001c0001t0001g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.195+3857T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243217867 | ||||||
| chr1:243218052
|
T | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.195+3672A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243218052 | ||||||
| chr1:243218074
|
C | G | 1 | a0002c0002t0003g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.195+3650G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243218074 | ||||||
| chr1:243218372
|
C | A | 1 | a0001c0007t0001g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.195+3352G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243218372 | ||||||
| chr1:243218391
|
G | A | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(281): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.195+3333C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243218391 | ||||||
| chr1:243218459
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.195+3265C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243218459 | ||||||
| chr1:243218906
|
G | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | NA18999.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.195+2818C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243218906 | ||||||
| chr1:243219064
|
T | C | 1 | a0002c0002t0003g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.195+2660A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243219064 | ||||||
| chr1:243219238
|
T | G | 1 | a0001c0001t0001g0276 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.195+2486A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243219238 | ||||||
| chr1:243219580
|
A | C | 1 | a0001c0001t0001g0060 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.195+2144T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243219580 | ||||||
| chr1:243219599
|
C | T | 1 | a0001c0014t0001g0110 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.195+2125G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243219599 | ||||||
| chr1:243219660
|
A | G | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+2064T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243219660 | ||||||
| chr1:243219797
|
A | G | 1 | a0002c0019t0001g0131 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.195+1927T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243219797 | ||||||
| chr1:243219956
|
G | A | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+1768C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243219956 | ||||||
| chr1:243220284
|
C | T | 3 | a0003c0003t0003g0107a0003c0009t0003g0108a0003c0009t0003g0109 | 3 | HG02723.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.195+1440G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243220284 | ||||||
| chr1:243220333
|
G | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.195+1391C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243220333 | ||||||
| chr1:243220334
|
A | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.195+1390T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243220334 | ||||||
| chr1:243220359
|
A | G | 96 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.195+1365T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243220359 | ||||||
| chr1:243220390
|
T | C | 4 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(1): Show | 4 | HG02818.hp2 HG03041.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+1334A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243220390 | ||||||
| chr1:243220539
|
A | G | 1 | a0001c0001t0001g0244 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.195+1185T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243220539 | ||||||
| chr1:243220553
|
T | A | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(277): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.195+1171A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243220553 | ||||||
| chr1:243220706
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(2): Show | 6 | HG00140.hp2 HG00280.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+1018G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243220706 | ||||||
| chr1:243220846
|
T | C | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.195+878A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243220846 | ||||||
| chr1:243220863
|
C | T | 25 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0106others(22): Show | 25 | HG01106.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.195+861G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243220863 | ||||||
| chr1:243220985
|
G | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(1): Show | 4 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+739C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243220985 | ||||||
| chr1:243221012
|
C | T | 1 | a0002c0002t0001g0185 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.195+712G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243221012 | ||||||
| chr1:243221030
|
C | CT | 16 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(13): Show | 16 | HG01261.hp2 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.195+693dupA | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243221030 | ||||||
| chr1:243221057
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.195+667A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243221057 | ||||||
| chr1:243221064
|
G | A | 1 | a0002c0002t0001g0185 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.195+660C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243221064 | ||||||
| chr1:243221076
|
G | C | 1 | a0002c0004t0001g0136 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.195+648C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243221076 | ||||||
| chr1:243221088
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(258): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.195+636A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243221088 | ||||||
| chr1:243221093
|
C | G | 1 | a0001c0001t0001g0282 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.195+631G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243221093 | ||||||
| chr1:243221124
|
A | C | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.195+600T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243221124 | ||||||
| chr1:243221144
|
A | C | 1 | a0004c0005t0001g0201 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.195+580T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243221144 | ||||||
| chr1:243221147
|
A | C | 1 | a0004c0005t0001g0201 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.195+577T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243221147 | ||||||
| chr1:243221222
|
A | T | 1 | a0001c0001t0001g0022 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.195+502T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243221222 | ||||||
| chr1:243221464
|
A | C | 33 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0106others(30): Show | 33 | HG01106.hp1 HG01884.hp2 HG01981.hp1 others(30): Show |
intron_variant | MODIFIER | c.195+260T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 3/19 | chr1 | 243221464 | ||||||
| chr1:243221954
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.106-141G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243221954 | ||||||
| chr1:243221955
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.106-142C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243221955 | ||||||
| chr1:243222005
|
A | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(141): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.106-192T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243222005 | ||||||
| chr1:243222172
|
A | G | 1 | a0002c0002t0001g0175 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.106-359T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243222172 | ||||||
| chr1:243222328
|
C | T | 10 | a0003c0003t0003g0149a0003c0003t0003g0150a0003c0003t0003g0151others(7): Show | 10 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.106-515G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243222328 | ||||||
| chr1:243222334
|
A | G | 130 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(127): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.106-521T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243222334 | ||||||
| chr1:243222391
|
T | C | 5 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0066others(2): Show | 5 | HG01099.hp1 HG01261.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-578A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243222391 | ||||||
| chr1:243222658
|
A | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.106-845T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243222658 | ||||||
| chr1:243222677
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.106-864C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243222677 | ||||||
| chr1:243222712
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.106-899T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243222712 | ||||||
| chr1:243222722
|
T | C | 1 | a0003c0003t0003g0161 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.106-909A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243222722 | ||||||
| chr1:243222734
|
T | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(94): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.106-921A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243222734 | ||||||
| chr1:243222890
|
C | A | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-1077G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243222890 | ||||||
| chr1:243223007
|
T | C | 27 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0106others(24): Show | 27 | HG01106.hp1 HG01884.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.106-1194A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243223007 | ||||||
| chr1:243223010
|
G | A | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(277): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.106-1197C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243223010 | ||||||
| chr1:243223417
|
G | A | 1 | a0001c0014t0001g0110 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.106-1604C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243223417 | ||||||
| chr1:243223463
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.106-1650A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243223463 | ||||||
| chr1:243223691
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.105+1485C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243223691 | ||||||
| chr1:243224274
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.105+902A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243224274 | ||||||
| chr1:243224386
|
G | A | 2 | a0001c0007t0001g0099a0001c0007t0001g0100 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.105+790C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243224386 | ||||||
| chr1:243224464
|
A | AAG | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.105+711_105+712ins others(2): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243224464 | ||||||
| chr1:243224486
|
G | A | 144 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(141): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.105+690C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243224486 | ||||||
| chr1:243225068
|
A | T | 129 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.105+108T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 2/19 | chr1 | 243225068 | ||||||
| chr1:243225341
|
A | G | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-41-20T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243225341 | ||||||
| chr1:243225557
|
G | A | 1 | a0002c0019t0001g0131 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-41-236C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243225557 | ||||||
| chr1:243225579
|
T | C | 32 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0106others(29): Show | 32 | HG01106.hp1 HG01884.hp2 HG01981.hp1 others(29): Show |
intron_variant | MODIFIER | c.-41-258A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243225579 | ||||||
| chr1:243225876
|
G | C | 7 | a0002c0002t0001g0165a0002c0002t0001g0167a0002c0002t0001g0168others(4): Show | 7 | HG00408.hp1 HG00423.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.-41-555C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243225876 | ||||||
| chr1:243225967
|
A | ATATC | 23 | a0002c0002t0001g0003a0002c0002t0001g0163a0002c0002t0001g0164others(20): Show | 24 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.-41-650_-41-647dup others(4): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243225967 | ||||||
| chr1:243225986
|
T | G | 3 | a0001c0001t0002g0061a0001c0001t0002g0092a0001c0001t0002g0093 | 3 | HG00738.hp2 HG02145.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-41-665A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243225986 | ||||||
| chr1:243225992
|
T | TACACGTA others(21): Show |
2 | a0001c0001t0003g0112a0002c0004t0001g0130 | 2 | NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-41-699_-41-672dup others(28): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243225992 | ||||||
| chr1:243225992
|
TACACGTA others(21): Show |
T | 3 | a0001c0001t0001g0006a0001c0001t0001g0237a0001c0001t0001g0280 | 4 | HG02735.hp1 HG03017.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41-699_-41-672del others(28): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243225992 | ||||||
| chr1:243226038
|
T | C | 2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | NA18964.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-41-717A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226038 | ||||||
| chr1:243226049
|
A | C | 3 | a0002c0002t0001g0003a0002c0002t0001g0183a0002c0002t0001g0184 | 4 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41-728T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226049 | ||||||
| chr1:243226058
|
G | GAT | 144 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(141): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-41-739_-41-738dup others(2): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226058 | ||||||
| chr1:243226058
|
G | GATATAGA others(33): Show |
3 | a0001c0001t0002g0105a0006c0008t0002g0101a0006c0008t0002g0102 | 3 | HG02109.hp1 HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-41-738_-41-737ins others(40): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226058 | ||||||
| chr1:243226058
|
G | GATATATA others(33): Show |
12 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0106others(9): Show | 12 | HG01106.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-41-738_-41-737ins others(40): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226058 | ||||||
| chr1:243226058
|
G | GATATATA others(71): Show |
1 | a0003c0009t0003g0109 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-41-738_-41-737ins others(78): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226058 | ||||||
| chr1:243226058
|
G | GATATATA others(31): Show |
10 | a0003c0003t0003g0149a0003c0003t0003g0150a0003c0003t0003g0151others(7): Show | 10 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-41-738_-41-737ins others(38): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226058 | ||||||
| chr1:243226063
|
A | ATT | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 117 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-41-743_-41-742ins others(2): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226063 | ||||||
| chr1:243226073
|
A | C | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-41-752T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226073 | ||||||
| chr1:243226137
|
GTA | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 115 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.-41-818_-41-817del others(2): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226137 | ||||||
| chr1:243226157
|
A | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.-41-836T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226157 | ||||||
| chr1:243226165
|
ATAGATAT others(23): Show |
A | 1 | a0002c0002t0001g0177 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-41-874_-41-845del others(30): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226165 | ||||||
| chr1:243226181
|
C | A | 1 | a0001c0001t0001g0138 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-41-860G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226181 | ||||||
| chr1:243226184
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-41-863C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226184 | ||||||
| chr1:243226185
|
A | G | 2 | a0001c0001t0001g0056a0001c0001t0009g0057 | 2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-41-864T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226185 | ||||||
| chr1:243226187
|
A | ATATATAC others(1): Show |
14 | a0001c0001t0001g0137a0001c0001t0001g0140a0001c0001t0001g0141others(11): Show | 14 | HG01261.hp2 HG02280.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-41-867_-41-866ins others(8): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226187 | ||||||
| chr1:243226187
|
A | ATATATAC others(23): Show |
1 | a0001c0001t0001g0139 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-41-867_-41-866ins others(30): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226187 | ||||||
| chr1:243226194
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(235): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.-41-873A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226194 | ||||||
| chr1:243226195
|
CTAGATAT others(1): Show |
C | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(235): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.-41-882_-41-875del others(8): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226195 | ||||||
| chr1:243226203
|
A | ATATGCC | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-41-883_-41-882ins others(6): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226203 | ||||||
| chr1:243226604
|
T | TA | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0040 | 3 | NA18982.hp1 NA19002.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.-41-1284dupT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226604 | ||||||
| chr1:243226627
|
T | G | 1 | a0001c0001t0001g0222 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-41-1306A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226627 | ||||||
| chr1:243226807
|
C | T | 3 | a0001c0001t0001g0074a0002c0002t0001g0164a0002c0002t0001g0171 | 3 | HG03927.hp1 NA18971.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-41-1486G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226807 | ||||||
| chr1:243226946
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0294 | 2 | NA18971.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-41-1625C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243226946 | ||||||
| chr1:243227045
|
C | T | 2 | a0001c0001t0003g0112a0001c0014t0001g0110 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-41-1724G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243227045 | ||||||
| chr1:243227266
|
C | CA | 96 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.-41-1946dupT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243227266 | ||||||
| chr1:243227411
|
C | G | 1 | a0001c0001t0001g0222 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-41-2090G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243227411 | ||||||
| chr1:243227523
|
A | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 121 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-41-2202T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243227523 | ||||||
| chr1:243227820
|
C | G | 1 | a0001c0001t0001g0072 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-41-2499G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243227820 | ||||||
| chr1:243227829
|
T | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(257): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.-41-2508A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243227829 | ||||||
| chr1:243228332
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(257): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.-41-3011A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243228332 | ||||||
| chr1:243228567
|
C | T | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41-3246G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243228567 | ||||||
| chr1:243229018
|
T | C | 3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0111 | 3 | HG02451.hp1 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-41-3697A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243229018 | ||||||
| chr1:243229271
|
G | A | 9 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0106others(6): Show | 9 | HG01106.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-41-3950C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243229271 | ||||||
| chr1:243229312
|
T | C | 1 | a0002c0004t0001g0136 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-41-3991A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243229312 | ||||||
| chr1:243229366
|
A | G | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-41-4045T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243229366 | ||||||
| chr1:243229396
|
G | A | 1 | a0003c0003t0003g0154 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-41-4075C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243229396 | ||||||
| chr1:243229425
|
G | GA | 26 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0106others(23): Show | 26 | HG01106.hp1 HG01884.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-41-4105_-41-4104i others(3): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243229425 | ||||||
| chr1:243229426
|
G | A | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(276): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-41-4105C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243229426 | ||||||
| chr1:243229701
|
T | C | 1 | a0001c0001t0001g0260 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-41-4380A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243229701 | ||||||
| chr1:243229747
|
A | C | 1 | a0001c0001t0002g0082 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-41-4426T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243229747 | ||||||
| chr1:243229761
|
G | C | 15 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(12): Show | 15 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-41-4440C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243229761 | ||||||
| chr1:243229867
|
C | T | 1 | a0001c0001t0002g0232 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-41-4546G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243229867 | ||||||
| chr1:243229889
|
C | G | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41-4568G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243229889 | ||||||
| chr1:243230014
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-41-4693C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243230014 | ||||||
| chr1:243230213
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-41-4892C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243230213 | ||||||
| chr1:243230351
|
C | CA | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 121 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-41-5031dupT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243230351 | ||||||
| chr1:243230421
|
T | C | 1 | a0002c0002t0001g0167 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-41-5100A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243230421 | ||||||
| chr1:243230451
|
A | C | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41-5130T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243230451 | ||||||
| chr1:243230490
|
A | G | 1 | a0002c0002t0003g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-41-5169T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243230490 | ||||||
| chr1:243230540
|
T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 121 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-41-5219A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243230540 | ||||||
| chr1:243230757
|
G | A | 1 | a0002c0002t0001g0180 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-41-5436C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243230757 | ||||||
| chr1:243230791
|
C | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.-41-5470G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243230791 | ||||||
| chr1:243231099
|
G | GA | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 117 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-41-5779dupT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231099 | ||||||
| chr1:243231099
|
GA | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.-41-5779delT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231099 | ||||||
| chr1:243231153
|
G | GCAT | 11 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0159others(8): Show | 11 | HG01123.hp2 HG01261.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-41-5835_-41-5833d others(5): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231153 | ||||||
| chr1:243231153
|
G | GCATCAT | 4 | a0001c0001t0001g0139a0001c0001t0002g0105a0002c0002t0001g0163others(1): Show | 4 | HG01192.hp1 HG01993.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41-5838_-41-5833d others(8): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231153 | ||||||
| chr1:243231153
|
GCAT | G | 82 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(79): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.-41-5835_-41-5833d others(5): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231153 | ||||||
| chr1:243231153
|
GCATCATC others(2): Show |
G | 6 | a0001c0001t0001g0040a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG00741.hp1 HG01123.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41-5841_-41-5833d others(11): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231153 | ||||||
| chr1:243231153
|
GCATCATC others(5): Show |
G | 1 | a0001c0001t0001g0010 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-41-5844_-41-5833d others(14): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231153 | ||||||
| chr1:243231187
|
CATCATT | C | 23 | a0001c0001t0001g0162a0001c0001t0001g0203a0001c0001t0001g0264others(20): Show | 23 | HG00408.hp2 HG00558.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.-41-5872_-41-5867d others(8): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231187 | ||||||
| chr1:243231190
|
C | CATCATCA others(5): Show |
1 | a0002c0002t0001g0165 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-41-5870_-41-5869i others(14): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231190 | ||||||
| chr1:243231190
|
C | CATCATCA others(2): Show |
10 | a0002c0002t0001g0164a0002c0002t0001g0166a0002c0002t0001g0169others(7): Show | 10 | HG00408.hp1 HG00423.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.-41-5870_-41-5869i others(11): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231190 | ||||||
| chr1:243231190
|
C | CATCATT | 6 | a0001c0001t0003g0112a0002c0002t0001g0167a0002c0002t0001g0175others(3): Show | 6 | HG00140.hp1 HG02056.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41-5870_-41-5869i others(8): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231190 | ||||||
| chr1:243231190
|
C | CATT | 6 | a0002c0002t0001g0168a0002c0002t0001g0179a0002c0018t0001g0122others(3): Show | 6 | HG02280.hp1 HG02622.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41-5872_-41-5870d others(5): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231190 | ||||||
| chr1:243231190
|
C | T | 20 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0116others(17): Show | 20 | HG01109.hp1 HG01884.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.-41-5869G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231190 | ||||||
| chr1:243231190
|
CATT | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0120others(75): Show | 83 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.-41-5872_-41-5870d others(5): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231190 | ||||||
| chr1:243231193
|
T | C | 11 | a0001c0001t0001g0006a0001c0001t0001g0195a0001c0001t0001g0212others(8): Show | 12 | HG00597.hp1 HG00741.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.-41-5872A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231193 | ||||||
| chr1:243231196
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-41-5875A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231196 | ||||||
| chr1:243231218
|
A | T | 1 | a0001c0001t0001g0236 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-41-5897T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231218 | ||||||
| chr1:243231249
|
T | C | 15 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(12): Show | 15 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-41-5928A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231249 | ||||||
| chr1:243231571
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-41-6250A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231571 | ||||||
| chr1:243231713
|
T | C | 2 | a0003c0009t0003g0108a0003c0009t0003g0109 | 2 | HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-41-6392A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231713 | ||||||
| chr1:243231944
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-41-6623G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243231944 | ||||||
| chr1:243232054
|
C | T | 2 | a0002c0002t0001g0164a0002c0002t0001g0171 | 2 | NA18971.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-41-6733G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243232054 | ||||||
| chr1:243232202
|
C | G | 1 | a0001c0001t0001g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-41-6881G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243232202 | ||||||
| chr1:243232582
|
T | C | 1 | a0001c0001t0001g0041 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-41-7261A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243232582 | ||||||
| chr1:243232645
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-41-7324G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243232645 | ||||||
| chr1:243232817
|
C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.-41-7496G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243232817 | ||||||
| chr1:243232830
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-41-7509T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243232830 | ||||||
| chr1:243232958
|
G | C | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-41-7637C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243232958 | ||||||
| chr1:243233024
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 117 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-41-7703G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243233024 | ||||||
| chr1:243233375
|
G | C | 3 | a0001c0001t0002g0218a0001c0001t0002g0273a0001c0001t0002g0274 | 3 | NA18964.hp1 NA18983.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.-41-8054C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243233375 | ||||||
| chr1:243233412
|
T | TC | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(252): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.-41-8092_-41-8091i others(3): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243233412 | ||||||
| chr1:243233462
|
G | A | 1 | a0001c0001t0002g0061 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-41-8141C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243233462 | ||||||
| chr1:243233486
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-41-8165G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243233486 | ||||||
| chr1:243233515
|
C | T | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-41-8194G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243233515 | ||||||
| chr1:243233562
|
T | A | 1 | a0001c0001t0005g0064 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-41-8241A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243233562 | ||||||
| chr1:243233732
|
C | CA | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 116 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-41-8412dupT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243233732 | ||||||
| chr1:243233732
|
C | CAA | 20 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0219others(17): Show | 20 | HG01071.hp2 HG01358.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.-41-8413_-41-8412d others(4): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243233732 | ||||||
| chr1:243233732
|
C | CAAA | 7 | a0001c0001t0001g0212a0001c0001t0001g0285a0001c0001t0001g0286others(4): Show | 7 | HG00738.hp2 HG01169.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.-41-8414_-41-8412d others(5): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243233732 | ||||||
| chr1:243233741
|
A | T | 1 | a0002c0004t0012g0296 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-41-8420T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243233741 | ||||||
| chr1:243233742
|
AT | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(99): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.-41-8422delA | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243233742 | ||||||
| chr1:243233743
|
T | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(166): Show | 175 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.-41-8422A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243233743 | ||||||
| chr1:243233745
|
T | A | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(258): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.-41-8424A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243233745 | ||||||
| chr1:243233747
|
T | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(162): Show | 170 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.-41-8426A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243233747 | ||||||
| chr1:243233749
|
T | A | 33 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(30): Show | 33 | HG00597.hp1 HG01261.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.-41-8428A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243233749 | ||||||
| chr1:243233751
|
T | A | 1 | a0001c0001t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-41-8430A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243233751 | ||||||
| chr1:243233885
|
A | T | 2 | a0001c0001t0001g0162a0001c0007t0001g0158 | 2 | HG01891.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-41-8564T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243233885 | ||||||
| chr1:243233886
|
C | A | 23 | a0002c0002t0001g0003a0002c0002t0001g0163a0002c0002t0001g0164others(20): Show | 24 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.-41-8565G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243233886 | ||||||
| chr1:243234192
|
T | C | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41-8871A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243234192 | ||||||
| chr1:243234480
|
C | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.-41-9159G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243234480 | ||||||
| chr1:243234549
|
T | C | 1 | a0001c0001t0003g0123 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-41-9228A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243234549 | ||||||
| chr1:243234642
|
A | G | 1 | a0002c0002t0001g0185 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-41-9321T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243234642 | ||||||
| chr1:243234881
|
A | T | 1 | a0001c0001t0001g0015 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-41-9560T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243234881 | ||||||
| chr1:243234914
|
T | C | 4 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(1): Show | 4 | HG02818.hp2 HG03041.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41-9593A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243234914 | ||||||
| chr1:243235257
|
T | G | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-41-9936A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243235257 | ||||||
| chr1:243235304
|
C | G | 2 | a0006c0008t0002g0101a0006c0008t0002g0102 | 2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-41-9983G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243235304 | ||||||
| chr1:243236588
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | NA19068.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-41-11267C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243236588 | ||||||
| chr1:243237400
|
C | T | 1 | a0001c0001t0002g0187 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-41-12079G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243237400 | ||||||
| chr1:243237630
|
G | A | 1 | a0002c0002t0003g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-41-12309C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243237630 | ||||||
| chr1:243237690
|
G | A | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41-12369C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243237690 | ||||||
| chr1:243237741
|
T | G | 4 | a0001c0001t0001g0080a0001c0001t0002g0081a0001c0001t0002g0082others(1): Show | 4 | HG02523.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41-12420A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243237741 | ||||||
| chr1:243237774
|
G | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0090 | 2 | HG01358.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-41-12453C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243237774 | ||||||
| chr1:243237841
|
G | T | 1 | a0001c0001t0001g0006 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-41-12520C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243237841 | ||||||
| chr1:243237960
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-41-12639G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243237960 | ||||||
| chr1:243238172
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-41-12851G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243238172 | ||||||
| chr1:243238342
|
C | T | 3 | a0001c0001t0003g0123a0001c0001t0003g0124a0002c0018t0001g0122 | 3 | HG01109.hp1 HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-41-13021G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243238342 | ||||||
| chr1:243238452
|
C | T | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(283): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-41-13131G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243238452 | ||||||
| chr1:243238534
|
C | T | 1 | a0001c0001t0003g0123 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-41-13213G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243238534 | ||||||
| chr1:243238677
|
A | G | 1 | a0001c0014t0001g0110 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-41-13356T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243238677 | ||||||
| chr1:243238695
|
C | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 114 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.-41-13374G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243238695 | ||||||
| chr1:243239000
|
T | C | 3 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289 | 3 | HG01071.hp2 HG01169.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-41-13679A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243239000 | ||||||
| chr1:243239419
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 115 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.-41-14098C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243239419 | ||||||
| chr1:243239919
|
AG | A | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-41-14599delC | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243239919 | ||||||
| chr1:243239922
|
T | A | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-41-14601A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243239922 | ||||||
| chr1:243239991
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.-41-14670C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243239991 | ||||||
| chr1:243240038
|
C | A | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-41-14717G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243240038 | ||||||
| chr1:243240157
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-41-14836C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243240157 | ||||||
| chr1:243240265
|
A | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(285): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-42+14775T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243240265 | ||||||
| chr1:243240633
|
A | AT | 15 | a0001c0001t0002g0126a0001c0001t0003g0123a0001c0001t0003g0124others(12): Show | 15 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-42+14406dupA | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243240633 | ||||||
| chr1:243240633
|
AT | A | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(256): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-42+14406delA | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243240633 | ||||||
| chr1:243240633
|
ATT | A | 10 | a0001c0001t0001g0090a0001c0001t0001g0096a0001c0001t0001g0203others(7): Show | 10 | HG01496.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-42+14405_-42+1440 others(6): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243240633 | ||||||
| chr1:243240779
|
G | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0280 | 3 | HG03017.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-42+14261C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243240779 | ||||||
| chr1:243241102
|
A | C | 10 | a0003c0003t0003g0149a0003c0003t0003g0150a0003c0003t0003g0151others(7): Show | 10 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-42+13938T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243241102 | ||||||
| chr1:243241129
|
C | T | 34 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(31): Show | 34 | HG01106.hp1 HG01884.hp2 HG01981.hp1 others(31): Show |
intron_variant | MODIFIER | c.-42+13911G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243241129 | ||||||
| chr1:243241278
|
G | T | 10 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(7): Show | 10 | HG01106.hp1 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-42+13762C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243241278 | ||||||
| chr1:243241284
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-42+13756C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243241284 | ||||||
| chr1:243241333
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-42+13707A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243241333 | ||||||
| chr1:243241428
|
A | C | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-42+13612T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243241428 | ||||||
| chr1:243241528
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-42+13512C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243241528 | ||||||
| chr1:243241580
|
A | G | 10 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(7): Show | 11 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-42+13460T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243241580 | ||||||
| chr1:243241677
|
C | A | 1 | a0001c0001t0002g0083 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-42+13363G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243241677 | ||||||
| chr1:243241786
|
T | C | 4 | a0002c0004t0001g0132a0002c0004t0001g0135a0002c0004t0001g0136others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42+13254A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243241786 | ||||||
| chr1:243241788
|
T | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | NA18978.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-42+13252A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243241788 | ||||||
| chr1:243241792
|
TA | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.-42+13247delT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243241792 | ||||||
| chr1:243241883
|
G | C | 1 | a0001c0001t0001g0203 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-42+13157C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243241883 | ||||||
| chr1:243241959
|
T | C | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+13081A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243241959 | ||||||
| chr1:243242155
|
G | A | 2 | a0003c0003t0003g0155a0003c0003t0003g0156 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-42+12885C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243242155 | ||||||
| chr1:243242166
|
T | C | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-42+12874A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243242166 | ||||||
| chr1:243242209
|
G | C | 1 | a0002c0002t0001g0180 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-42+12831C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243242209 | ||||||
| chr1:243242259
|
C | T | 2 | a0003c0009t0003g0108a0003c0009t0003g0109 | 2 | HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-42+12781G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243242259 | ||||||
| chr1:243242307
|
C | T | 3 | a0001c0001t0003g0123a0001c0001t0003g0124a0002c0018t0001g0122 | 3 | HG01109.hp1 HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-42+12733G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243242307 | ||||||
| chr1:243242312
|
G | A | 3 | a0001c0001t0003g0123a0001c0001t0003g0124a0002c0018t0001g0122 | 3 | HG01109.hp1 HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-42+12728C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243242312 | ||||||
| chr1:243242363
|
C | A | 4 | a0001c0007t0001g0099a0001c0007t0001g0100a0006c0008t0002g0101others(1): Show | 4 | HG02280.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42+12677G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243242363 | ||||||
| chr1:243242363
|
C | T | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+12677G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243242363 | ||||||
| chr1:243242420
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-42+12620C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243242420 | ||||||
| chr1:243242456
|
G | C | 1 | a0001c0001t0001g0222 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-42+12584C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243242456 | ||||||
| chr1:243242536
|
C | T | 1 | a0002c0002t0003g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-42+12504G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243242536 | ||||||
| chr1:243242653
|
C | T | 1 | a0001c0014t0001g0110 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-42+12387G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243242653 | ||||||
| chr1:243242825
|
C | G | 3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0111 | 3 | HG02451.hp1 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-42+12215G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243242825 | ||||||
| chr1:243243036
|
C | T | 2 | a0003c0009t0003g0108a0003c0009t0003g0109 | 2 | HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-42+12004G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243243036 | ||||||
| chr1:243243058
|
TACACCAC others(4): Show |
T | 1 | a0001c0001t0001g0284 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-42+11971_-42+1198 others(15): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243243058 | ||||||
| chr1:243243091
|
C | T | 5 | a0001c0001t0001g0211a0001c0001t0001g0221a0001c0001t0001g0227others(2): Show | 5 | HG03704.hp2 HG03927.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42+11949G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243243091 | ||||||
| chr1:243243167
|
T | G | 1 | a0001c0001t0008g0104 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-42+11873A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243243167 | ||||||
| chr1:243243497
|
G | GATTT | 27 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0140others(24): Show | 28 | HG00597.hp1 HG01361.hp2 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.-42+11539_-42+1154 others(8): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243243497 | ||||||
| chr1:243243497
|
G | GATTTATT others(1): Show |
22 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(19): Show | 22 | HG00609.hp1 HG01106.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-42+11535_-42+1154 others(12): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243243497 | ||||||
| chr1:243243497
|
GATTT | G | 122 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.-42+11539_-42+1154 others(8): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243243497 | ||||||
| chr1:243243579
|
A | G | 1 | a0002c0002t0001g0169 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-42+11461T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243243579 | ||||||
| chr1:243243678
|
C | T | 34 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(31): Show | 34 | HG01106.hp1 HG01884.hp2 HG01981.hp1 others(31): Show |
intron_variant | MODIFIER | c.-42+11362G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243243678 | ||||||
| chr1:243244065
|
C | T | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG02257.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-42+10975G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243244065 | ||||||
| chr1:243244198
|
G | T | 1 | a0002c0002t0003g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-42+10842C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243244198 | ||||||
| chr1:243244357
|
T | TCA | 23 | a0002c0002t0001g0003a0002c0002t0001g0163a0002c0002t0001g0164others(20): Show | 24 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.-42+10681_-42+1068 others(6): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243244357 | ||||||
| chr1:243244357
|
T | TCACA | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+10679_-42+1068 others(8): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243244357 | ||||||
| chr1:243244357
|
TCA | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(201): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.-42+10681_-42+1068 others(6): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243244357 | ||||||
| chr1:243244361
|
A | T | 1 | a0001c0015t0001g0223 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-42+10679T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243244361 | ||||||
| chr1:243244480
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.-42+10560G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243244480 | ||||||
| chr1:243244542
|
AG | A | 27 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(24): Show | 27 | HG01106.hp1 HG01884.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-42+10497delC | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243244542 | ||||||
| chr1:243244561
|
G | A | 2 | a0001c0001t0001g0281a0001c0001t0001g0284 | 2 | NA18962.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-42+10479C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243244561 | ||||||
| chr1:243244704
|
C | G | 1 | a0001c0001t0001g0222 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-42+10336G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243244704 | ||||||
| chr1:243244754
|
T | TA | 94 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.-42+10285dupT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243244754 | ||||||
| chr1:243244778
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-42+10262G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243244778 | ||||||
| chr1:243245372
|
G | A | 1 | a0001c0001t0002g0009 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-42+9668C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243245372 | ||||||
| chr1:243245475
|
G | A | 6 | a0001c0001t0001g0282a0001c0001t0001g0285a0001c0001t0001g0286others(3): Show | 6 | HG01071.hp2 HG01169.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+9565C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243245475 | ||||||
| chr1:243245730
|
CAAACAAA | C | 4 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(1): Show | 4 | HG02818.hp2 HG03041.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42+9303_-42+9309d others(9): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243245730 | ||||||
| chr1:243245760
|
C | CA | 12 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(9): Show | 12 | HG01106.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-42+9279dupT | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243245760 | ||||||
| chr1:243245850
|
C | T | 129 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.-42+9190G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243245850 | ||||||
| chr1:243245861
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.-42+9179G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243245861 | ||||||
| chr1:243245987
|
C | A | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-42+9053G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243245987 | ||||||
| chr1:243245987
|
C | T | 34 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(31): Show | 34 | HG01106.hp1 HG01884.hp2 HG01981.hp1 others(31): Show |
intron_variant | MODIFIER | c.-42+9053G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243245987 | ||||||
| chr1:243245989
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-42+9051A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243245989 | ||||||
| chr1:243246075
|
G | T | 1 | a0001c0001t0001g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-42+8965C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243246075 | ||||||
| chr1:243246226
|
C | CT | 41 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0050others(38): Show | 41 | HG01099.hp1 HG01169.hp1 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.-42+8813dupA | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243246226 | ||||||
| chr1:243246226
|
C | CTT | 13 | a0001c0001t0001g0094a0001c0014t0001g0110a0003c0003t0003g0149others(10): Show | 13 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-42+8812_-42+8813d others(4): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243246226 | ||||||
| chr1:243246226
|
C | CTTTT | 8 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0111others(5): Show | 8 | HG02109.hp1 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-42+8810_-42+8813d others(6): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243246226 | ||||||
| chr1:243246248
|
T | TC | 3 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0083 | 3 | HG02523.hp1 HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-42+8791_-42+8792i others(3): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243246248 | ||||||
| chr1:243246262
|
C | T | 1 | a0003c0003t0003g0103 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-42+8778G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243246262 | ||||||
| chr1:243246620
|
T | C | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-42+8420A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243246620 | ||||||
| chr1:243246624
|
AAGTT | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.-42+8412_-42+8415d others(6): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243246624 | ||||||
| chr1:243246906
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.-42+8134T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243246906 | ||||||
| chr1:243246908
|
G | GTAT | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 117 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-42+8129_-42+8131d others(5): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243246908 | ||||||
| chr1:243247021
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG00738.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.-42+8019G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243247021 | ||||||
| chr1:243247202
|
A | C | 1 | a0001c0001t0005g0114 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-42+7838T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243247202 | ||||||
| chr1:243247286
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-42+7754C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243247286 | ||||||
| chr1:243247510
|
C | T | 1 | a0001c0001t0002g0205 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-42+7530G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243247510 | ||||||
| chr1:243247516
|
A | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(252): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.-42+7524T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243247516 | ||||||
| chr1:243247643
|
C | T | 1 | a0011c0012t0001g0204 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-42+7397G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243247643 | ||||||
| chr1:243247718
|
G | A | 1 | a0002c0002t0003g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-42+7322C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243247718 | ||||||
| chr1:243247851
|
T | C | 1 | a0001c0014t0001g0110 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-42+7189A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243247851 | ||||||
| chr1:243247901
|
A | T | 1 | a0001c0001t0001g0203 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-42+7139T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243247901 | ||||||
| chr1:243247907
|
C | T | 3 | a0003c0003t0003g0107a0003c0009t0003g0108a0003c0009t0003g0109 | 3 | HG02723.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-42+7133G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243247907 | ||||||
| chr1:243248065
|
T | G | 23 | a0002c0002t0001g0003a0002c0002t0001g0163a0002c0002t0001g0164others(20): Show | 24 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.-42+6975A>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243248065 | ||||||
| chr1:243248084
|
G | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.-42+6956C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243248084 | ||||||
| chr1:243248091
|
G | T | 1 | a0002c0004t0001g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-42+6949C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243248091 | ||||||
| chr1:243248103
|
G | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 117 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-42+6937C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243248103 | ||||||
| chr1:243248162
|
G | A | 1 | a0004c0005t0001g0201 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-42+6878C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243248162 | ||||||
| chr1:243248269
|
A | G | 1 | a0001c0001t0002g0202 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-42+6771T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243248269 | ||||||
| chr1:243248395
|
T | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0294 | 2 | NA18971.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-42+6645A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243248395 | ||||||
| chr1:243248486
|
G | T | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-42+6554C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243248486 | ||||||
| chr1:243248909
|
T | C | 2 | a0002c0004t0001g0135a0002c0004t0001g0136 | 2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-42+6131A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243248909 | ||||||
| chr1:243249031
|
A | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-42+6009T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243249031 | ||||||
| chr1:243249115
|
A | C | 10 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(7): Show | 10 | HG01106.hp1 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-42+5925T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243249115 | ||||||
| chr1:243249121
|
G | T | 1 | a0001c0001t0002g0095 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-42+5919C>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243249121 | ||||||
| chr1:243249341
|
C | T | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42+5699G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243249341 | ||||||
| chr1:243249418
|
A | AAAAT | 6 | a0001c0001t0001g0049a0002c0002t0001g0163a0002c0002t0001g0185others(3): Show | 6 | HG01192.hp1 HG01934.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42+5618_-42+5621d others(6): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243249418 | ||||||
| chr1:243249418
|
A | AAAATAAA others(1): Show |
4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(1): Show | 4 | HG01071.hp1 HG01175.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42+5614_-42+5621d others(10): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243249418 | ||||||
| chr1:243249418
|
AAAAT | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 119 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.-42+5618_-42+5621d others(6): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243249418 | ||||||
| chr1:243249418
|
AAAATAAA others(9): Show |
A | 34 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(31): Show | 34 | HG01106.hp1 HG01884.hp2 HG01981.hp1 others(31): Show |
intron_variant | MODIFIER | c.-42+5606_-42+5621d others(18): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243249418 | ||||||
| chr1:243249634
|
T | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.-42+5406A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243249634 | ||||||
| chr1:243249823
|
C | T | 48 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(45): Show | 49 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.-42+5217G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243249823 | ||||||
| chr1:243250348
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-42+4692C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243250348 | ||||||
| chr1:243250523
|
A | C | 1 | a0001c0001t0004g0191 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-42+4517T>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243250523 | ||||||
| chr1:243250657
|
C | T | 34 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(31): Show | 34 | HG01106.hp1 HG01884.hp2 HG01981.hp1 others(31): Show |
intron_variant | MODIFIER | c.-42+4383G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243250657 | ||||||
| chr1:243250764
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 117 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-42+4276G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243250764 | ||||||
| chr1:243250922
|
T | C | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-42+4118A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243250922 | ||||||
| chr1:243251010
|
T | C | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-42+4030A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243251010 | ||||||
| chr1:243251143
|
A | G | 4 | a0001c0007t0001g0099a0001c0007t0001g0100a0006c0008t0002g0101others(1): Show | 4 | HG02280.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42+3897T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243251143 | ||||||
| chr1:243251272
|
T | C | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(1): Show | 4 | HG01071.hp1 HG01175.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42+3768A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243251272 | ||||||
| chr1:243251362
|
A | G | 1 | a0001c0001t0005g0114 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-42+3678T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243251362 | ||||||
| chr1:243251389
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.-42+3651T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243251389 | ||||||
| chr1:243251410
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.-42+3630T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243251410 | ||||||
| chr1:243251417
|
G | A | 31 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0106others(28): Show | 31 | HG01106.hp1 HG01884.hp2 HG01981.hp1 others(28): Show |
intron_variant | MODIFIER | c.-42+3623C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243251417 | ||||||
| chr1:243251660
|
C | T | 1 | a0002c0018t0001g0122 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-42+3380G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243251660 | ||||||
| chr1:243251762
|
C | G | 34 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(31): Show | 34 | HG01106.hp1 HG01884.hp2 HG01981.hp1 others(31): Show |
intron_variant | MODIFIER | c.-42+3278G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243251762 | ||||||
| chr1:243252194
|
T | C | 1 | a0001c0001t0001g0284 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-42+2846A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243252194 | ||||||
| chr1:243252279
|
G | A | 5 | a0002c0002t0001g0003a0002c0002t0001g0183a0002c0002t0001g0184others(2): Show | 6 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42+2761C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243252279 | ||||||
| chr1:243252832
|
G | A | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 14 | HG01261.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-42+2208C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243252832 | ||||||
| chr1:243252919
|
T | C | 1 | a0001c0001t0003g0124 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-42+2121A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243252919 | ||||||
| chr1:243253055
|
C | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-42+1985G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243253055 | ||||||
| chr1:243253202
|
T | C | 1 | a0001c0001t0005g0114 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-42+1838A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243253202 | ||||||
| chr1:243253205
|
G | A | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(276): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-42+1835C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243253205 | ||||||
| chr1:243253223
|
T | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(127): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.-42+1817A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243253223 | ||||||
| chr1:243253371
|
G | A | 5 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0288others(2): Show | 5 | HG01071.hp2 HG01169.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42+1669C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243253371 | ||||||
| chr1:243253490
|
T | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.-42+1550A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243253490 | ||||||
| chr1:243253569
|
A | G | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(276): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-42+1471T>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243253569 | ||||||
| chr1:243253593
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-42+1447A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243253593 | ||||||
| chr1:243253680
|
T | C | 2 | a0001c0001t0002g0092a0001c0001t0002g0093 | 2 | HG00738.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-42+1360A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243253680 | ||||||
| chr1:243253989
|
T | A | 1 | a0001c0001t0001g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-42+1051A>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243253989 | ||||||
| chr1:243254022
|
T | C | 296 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(293): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.-42+1018A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243254022 | ||||||
| chr1:243254187
|
A | AAAAT | 23 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(20): Show | 23 | HG01261.hp2 HG01884.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.-42+849_-42+852dup others(4): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243254187 | ||||||
| chr1:243254187
|
A | AAAATAAA others(1): Show |
17 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0106others(14): Show | 17 | HG02109.hp1 HG02145.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.-42+845_-42+852dup others(8): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243254187 | ||||||
| chr1:243254187
|
A | AAAATAAA others(5): Show |
8 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0001g0116others(5): Show | 8 | HG01106.hp1 HG01981.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-42+841_-42+852dup others(12): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243254187 | ||||||
| chr1:243254187
|
A | AAAATAAA others(9): Show |
1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-42+837_-42+852dup others(16): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243254187 | ||||||
| chr1:243254187
|
AAAAT | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(125): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-42+849_-42+852del others(4): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243254187 | ||||||
| chr1:243254320
|
A | T | 1 | a0001c0001t0001g0010 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-42+720T>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243254320 | ||||||
| chr1:243254525
|
CCAA | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(87): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.-42+512_-42+514del others(3): Show |
CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243254525 | ||||||
| chr1:243254530
|
C | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(87): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.-42+510G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243254530 | ||||||
| chr1:243254551
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(280): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-42+489A>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243254551 | ||||||
| chr1:243254563
|
G | C | 1 | a0001c0001t0001g0113 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-42+477C>G | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243254563 | ||||||
| chr1:243254572
|
G | A | 1 | a0001c0001t0005g0114 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-42+468C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243254572 | ||||||
| chr1:243254590
|
G | A | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG01981.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42+450C>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243254590 | ||||||
| chr1:243254761
|
C | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 120 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.-42+279G>T | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243254761 | ||||||
| chr1:243254768
|
GC | G | 3 | a0001c0001t0003g0123a0001c0001t0003g0124a0002c0018t0001g0122 | 3 | HG01109.hp1 HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-42+271delG | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243254768 | ||||||
| chr1:243254822
|
C | G | 1 | a0002c0002t0003g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-42+218G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243254822 | ||||||
| chr1:243254829
|
C | G | 1 | a0001c0001t0002g0009 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-42+211G>C | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243254829 | ||||||
| chr1:243254847
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | NA18999.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-42+193G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243254847 | ||||||
| chr1:243254880
|
C | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(112): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.-42+160G>A | CEP170 | ENSG00000143702.16 | transcript | ENST00000366542.6 | protein_coding | 1/19 | chr1 | 243254880 |