Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 79598 |
|---|---|
| ensemblid | ENSG00000182504.12 |
| hgncid | 26244 |
| symbol | CEP97 |
| name | centrosomal protein 97 |
| refseq_nuc | NM_024548.4 |
| refseq_prot | NP_078824.2 |
| ensembl_nuc | ENST00000341893.8 |
| ensembl_prot | ENSP00000342510.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 101724614 |
| end | 101770562 |
| strand | + |
| ver | v1.2 |
| region | chr3:101724614-101770562 |
| region5000 | chr3:101719614-101775562 |
| regionname0 | CEP97_chr3_101724614_101770562 |
| regionname5000 | CEP97_chr3_101719614_101775562 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 865 | 336 | 84 | 57 | 151 | 11 | 31 | 115 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0002 | 0/0 | 865 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0003 | 0/0 | 865 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0004 | 0/0 | 865 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0005 | 0/0 | 865 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0006 | 0/0 | 865 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0007 | 0/0 | 607 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0008 | 0/0 | 865 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0009 | 0/0 | 865 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0010 | 0/0 | 865 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0011 | 0/0 | 865 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0012 | 0/0 | 865 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0013 | 0/0 | 865 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2598 | 298 | 69 | 47 | 149 | 6 | 26 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| c0002 | 1/0 | 2598 | 34 | 13 | 10 | 2 | 4 | 4 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| c0003 | 0/0 | 2598 | 3 | 2 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| c0004 | 0/0 | 2598 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| c0005 | 0/0 | 2598 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| c0006 | 0/0 | 2598 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| c0007 | 0/0 | 2598 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| c0008 | 0/0 | 2598 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| c0009 | 0/0 | 2598 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| c0010 | 0/0 | 2598 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| c0011 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| c0012 | 0/0 | 2598 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| c0013 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| c0014 | 0/0 | 2598 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| c0015 | 0/0 | 2598 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| c0016 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| c0017 | 0/0 | 2598 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| c0018 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 5075 | 140 | 25 | 26 | 70 | 2 | 17 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0002 | 0/0 | 5075 | 103 | 20 | 19 | 54 | 3 | 7 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0003 | 0/0 | 5075 | 22 | 8 | 9 | 0 | 4 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0004 | 0/0 | 5077 | 20 | 4 | 3 | 7 | 3 | 3 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0005 | 0/0 | 5075 | 12 | 1 | 0 | 11 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0006 | 0/0 | 5077 | 7 | 5 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0007 | 0/0 | 5079 | 6 | 6 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0008 | 0/0 | 5075 | 5 | 0 | 1 | 2 | 0 | 2 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0009 | 1/0 | 5075 | 5 | 4 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0010 | 0/0 | 5079 | 3 | 3 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0011 | 0/0 | 5076 | 3 | 1 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0012 | 0/0 | 5075 | 3 | 0 | 0 | 3 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0013 | 0/0 | 5079 | 2 | 2 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0014 | 0/0 | 5078 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0015 | 0/0 | 5075 | 2 | 2 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0016 | 0/0 | 5075 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0017 | 0/0 | 5077 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0018 | 0/0 | 5077 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0019 | 0/1 | 5075 | 1 | 0 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0020 | 0/0 | 5075 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0021 | 0/0 | 5075 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0022 | 0/0 | 5075 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0023 | 0/0 | 5075 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0024 | 0/0 | 5075 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0025 | 0/0 | 5075 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0026 | 0/0 | 5075 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0027 | 0/0 | 5075 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0028 | 0/0 | 5076 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0029 | 0/0 | 5075 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0030 | 0/0 | 5075 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0031 | 0/0 | 5075 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| t0032 | 0/0 | 5075 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0007 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0019 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0260 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2598 | 298 | 69 | 47 | 149 | 6 | 26 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0002 | 1/0 | 2598 | 34 | 13 | 10 | 2 | 4 | 4 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0008 | 0/0 | 2598 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0013 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0015 | 0/0 | 2598 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0016 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0002c0003 | 0/0 | 2598 | 3 | 2 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0003c0005 | 0/0 | 2598 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0004c0004 | 0/0 | 2598 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0005c0006 | 0/0 | 2598 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0006c0007 | 0/0 | 2598 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0007c0014 | 0/0 | 2598 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0008c0012 | 0/0 | 2598 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0009c0011 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0010c0010 | 0/0 | 2598 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0011c0009 | 0/0 | 2598 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0012c0017 | 0/0 | 2598 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0013c0018 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7672 | 130 | 23 | 25 | 65 | 2 | 15 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0002 | 0/0 | 7672 | 96 | 18 | 17 | 52 | 2 | 7 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0004 | 0/0 | 7674 | 19 | 4 | 3 | 7 | 2 | 3 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0005 | 0/0 | 7672 | 12 | 1 | 0 | 11 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0006 | 0/0 | 7674 | 7 | 5 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0007 | 0/0 | 7676 | 6 | 6 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0010 | 0/0 | 7676 | 3 | 3 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0011 | 0/0 | 7673 | 3 | 1 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0012 | 0/0 | 7672 | 3 | 0 | 0 | 3 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0013 | 0/0 | 7676 | 2 | 2 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0014 | 0/0 | 7675 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0015 | 0/0 | 7672 | 2 | 2 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0016 | 0/0 | 7672 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0017 | 0/0 | 7674 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0019 | 0/1 | 7672 | 1 | 0 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0021 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0022 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0023 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0024 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0025 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0026 | 0/0 | 7672 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0027 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0030 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0031 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0001t0032 | 0/0 | 7672 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0002t0003 | 0/0 | 7672 | 22 | 8 | 9 | 0 | 4 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0002t0008 | 0/0 | 7672 | 5 | 0 | 1 | 2 | 0 | 2 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0002t0009 | 1/0 | 7672 | 5 | 4 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0002t0018 | 0/0 | 7674 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0002t0028 | 0/0 | 7673 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0008t0004 | 0/0 | 7674 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0013t0020 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0015t0001 | 0/0 | 7672 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0001c0016t0029 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0002c0003t0002 | 0/0 | 7672 | 3 | 2 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0003c0005t0001 | 0/0 | 7672 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0004c0004t0002 | 0/0 | 7672 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0005c0006t0002 | 0/0 | 7672 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0006c0007t0001 | 0/0 | 7672 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0007c0014t0001 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0008c0012t0001 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0009c0011t0001 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0010c0010t0001 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0011c0009t0001 | 0/0 | 7672 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0012c0017t0002 | 0/0 | 7672 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| a0013c0018t0001 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | copy fasta | chr3 | 101719614 | 101775562 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0004g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0005g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0006g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0006g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0007g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0010g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0010g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0010g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0011g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0011g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0011g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0012g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0012g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0012g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0013g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0013g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0014g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0014g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0015g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0015g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0016g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0017g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0019g0260 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0021g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0022g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0023g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0024g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0025g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0026g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0027g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0030g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0031g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0032g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0008g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0008g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0008g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0008g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0008g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0009g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0009g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0009g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0018g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0028g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0008t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0013t0020g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0015t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0016t0029g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0002c0003t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0002c0003t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0002c0003t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0003c0005t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0003c0005t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0004c0004t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0005c0006t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0006c0007t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0007c0014t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0008c0012t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0009c0011t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0010c0010t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0011c0009t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0012c0017t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0013c0018t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0187 | EUR | GBR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0080 | EUR | GBR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00280 | hp1 | a0001 | c0002 | t0003 | g0129 | EUR | FIN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0091 | EUR | FIN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0247 | EUR | FIN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00323 | hp2 | a0001 | c0008 | t0004 | g0075 | EUR | FIN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | CHS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | CHS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0070 | EAS | CHS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00609 | hp2 | a0001 | c0001 | t0006 | g0194 | EAS | CHS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | CHS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00621 | hp2 | a0003 | c0005 | t0001 | g0284 | EAS | CHS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00735 | hp2 | a0011 | c0009 | t0001 | g0032 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00738 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01069 | hp1 | a0012 | c0017 | t0002 | g0200 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0077 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0128 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0303 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01106 | hp1 | a0001 | c0002 | t0003 | g0136 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01175 | hp2 | a0001 | c0002 | t0003 | g0132 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0026 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0015 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01243 | hp2 | a0002 | c0003 | t0002 | g0209 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0015 | AMR | CLM | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01358 | hp1 | a0001 | c0001 | t0016 | g0023 | AMR | CLM | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01433 | hp2 | a0001 | c0002 | t0008 | g0120 | AMR | CLM | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01516 | hp1 | a0005 | c0006 | t0002 | g0007 | EUR | IBS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01516 | hp2 | a0001 | c0002 | t0003 | g0014 | EUR | IBS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0293 | EUR | IBS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01517 | hp2 | a0001 | c0002 | t0003 | g0014 | EUR | IBS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01884 | hp1 | a0002 | c0003 | t0002 | g0214 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01884 | hp2 | a0001 | c0001 | t0013 | g0110 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01943 | hp1 | a0001 | c0001 | t0026 | g0114 | AMR | PEL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0314 | AMR | PEL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PEL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0081 | AMR | PEL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02027 | hp1 | a0007 | c0014 | t0001 | g0051 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0217 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02071 | hp1 | a0001 | c0001 | t0021 | g0052 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0064 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02135 | hp1 | a0001 | c0001 | t0014 | g0071 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02135 | hp2 | a0001 | c0001 | t0006 | g0201 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0113 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CDX | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CDX | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | CDX | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0304 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02523 | hp1 | a0001 | c0001 | t0022 | g0067 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02572 | hp1 | a0013 | c0018 | t0001 | g0235 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0076 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02615 | hp1 | a0001 | c0016 | t0029 | g0104 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0107 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02622 | hp2 | a0001 | c0002 | t0009 | g0003 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0106 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02698 | hp1 | a0001 | c0002 | t0018 | g0118 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0105 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0084 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02809 | hp1 | a0001 | c0002 | t0009 | g0125 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02886 | hp1 | a0001 | c0002 | t0003 | g0137 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02895 | hp2 | a0002 | c0003 | t0002 | g0212 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ESN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ESN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | ESN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | ESN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02970 | hp2 | a0001 | c0002 | t0003 | g0130 | AFR | ESN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | ESN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | ESN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0309 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | MSL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03098 | hp2 | a0001 | c0002 | t0028 | g0138 | AFR | MSL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | ESN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03130 | hp2 | a0001 | c0001 | t0015 | g0242 | AFR | ESN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | ESN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | ESN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0316 | AFR | ESN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0135 | AFR | MSL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03225 | hp1 | a0001 | c0001 | t0013 | g0109 | AFR | MSL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03453 | hp1 | a0009 | c0011 | t0001 | g0142 | AFR | MSL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0216 | AFR | MSL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03486 | hp2 | a0001 | c0002 | t0003 | g0139 | AFR | MSL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | ESN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03516 | hp2 | a0001 | c0002 | t0003 | g0127 | AFR | ESN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03579 | hp1 | a0001 | c0001 | t0031 | g0122 | AFR | MSL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0218 | AFR | MSL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0087 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | STU | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03710 | hp1 | a0001 | c0002 | t0003 | g0133 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03834 | hp1 | a0001 | c0002 | t0008 | g0116 | SAS | BEB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03927 | hp1 | a0001 | c0001 | t0032 | g0024 | SAS | BEB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03942 | hp2 | a0001 | c0015 | t0001 | g0259 | SAS | BEB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | STU | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG04115 | hp2 | a0006 | c0007 | t0001 | g0055 | SAS | STU | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG04228 | hp1 | a0001 | c0002 | t0008 | g0124 | SAS | STU | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | YRI | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0061 | EAS | CHB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | CHB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18906 | hp1 | a0001 | c0001 | t0010 | g0112 | AFR | YRI | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0141 | AFR | YRI | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18941 | hp2 | a0001 | c0001 | t0030 | g0069 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18943 | hp1 | a0001 | c0001 | t0014 | g0008 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18944 | hp2 | a0001 | c0002 | t0008 | g0117 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18953 | hp1 | a0003 | c0005 | t0001 | g0231 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18954 | hp1 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18961 | hp2 | a0001 | c0001 | t0012 | g0301 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0068 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18966 | hp1 | a0004 | c0004 | t0002 | g0018 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18969 | hp2 | a0004 | c0004 | t0002 | g0018 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18972 | hp1 | a0001 | c0002 | t0008 | g0119 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18979 | hp2 | a0001 | c0001 | t0011 | g0271 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18988 | hp1 | a0001 | c0001 | t0027 | g0204 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18993 | hp2 | a0001 | c0001 | t0011 | g0252 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18999 | hp2 | a0001 | c0001 | t0024 | g0022 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19011 | hp1 | a0001 | c0001 | t0012 | g0300 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19030 | hp1 | a0001 | c0013 | t0020 | g0307 | AFR | LWK | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19043 | hp1 | a0001 | c0002 | t0009 | g0003 | AFR | LWK | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | LWK | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19055 | hp2 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19062 | hp2 | a0010 | c0010 | t0001 | g0248 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19070 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19080 | hp1 | a0001 | c0001 | t0005 | g0063 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19080 | hp2 | a0008 | c0012 | t0001 | g0233 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19087 | hp1 | a0001 | c0001 | t0012 | g0302 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19090 | hp2 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | YRI | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19240 | hp2 | a0001 | c0001 | t0011 | g0143 | AFR | YRI | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | ASW | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0315 | AFR | ASW | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0019 | EUR | TSI | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA20805 | hp2 | a0001 | c0002 | t0003 | g0134 | EUR | TSI | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02109 | hp2 | a0001 | c0001 | t0023 | g0103 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0111 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0131 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02559 | hp2 | a0001 | c0002 | t0009 | g0003 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03471 | hp1 | a0001 | c0002 | t0003 | g0140 | AFR | MSL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03471 | hp2 | a0001 | c0001 | t0015 | g0279 | AFR | MSL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | USA | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | USA | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | USA | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA20300 | hp2 | a0001 | c0001 | t0025 | g0282 | AFR | USA | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0093 | AFR | LWK | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA21309 | hp2 | a0001 | c0001 | t0017 | g0144 | AFR | LWK | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0019 | g0260 | REF | REF | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0009 | g0126 | REF | REF | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:101726726
|
G | A | 1 | a0005 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.176G>A | p.Arg59Gln | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 2/11 | 239/7672 | 176/2598 | 59/865 | chr3 | 101726726 | ||
| chr3:101727426
|
C | T | 1 | a0013 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.230C>T | p.Ala77Val | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 3/11 | 293/7672 | 230/2598 | 77/865 | chr3 | 101727426 | ||
| chr3:101727461
|
C | T | 1 | a0012 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.265C>T | p.His89Tyr | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 3/11 | 328/7672 | 265/2598 | 89/865 | chr3 | 101727461 | ||
| chr3:101732596
|
G | A | 1 | a0006 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.670G>A | p.Val224Ile | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/11 | 733/7672 | 670/2598 | 224/865 | chr3 | 101732596 | ||
| chr3:101757124
|
G | C | 1 | a0002 | 3 | HG01243.hp2 HG01884.hp1 HG02895.hp2 |
missense_variant | MODERATE | c.955G>C | p.Val319Leu | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 8/11 | 1018/7672 | 955/2598 | 319/865 | chr3 | 101757124 | ||
| chr3:101757792
|
T | A | 1 | a0004 | 2 | NA18966.hp1 NA18969.hp2 |
missense_variant | MODERATE | c.1186T>A | p.Cys396Ser | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/11 | 1249/7672 | 1186/2598 | 396/865 | chr3 | 101757792 | ||
| chr3:101757801
|
C | T | 1 | a0012 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.1195C>T | p.Leu399Phe | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/11 | 1258/7672 | 1195/2598 | 399/865 | chr3 | 101757801 | ||
| chr3:101757888
|
T | G | 1 | a0011 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.1282T>G | p.Leu428Val | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/11 | 1345/7672 | 1282/2598 | 428/865 | chr3 | 101757888 | ||
| chr3:101757973
|
T | C | 1 | a0010 | 1 | NA19062.hp2 | missense_variant | MODERATE | c.1367T>C | p.Leu456Ser | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/11 | 1430/7672 | 1367/2598 | 456/865 | chr3 | 101757973 | ||
| chr3:101758006
|
T | A | 1 | a0003 | 2 | HG00621.hp2 NA18953.hp1 |
missense_variant | MODERATE | c.1400T>A | p.Met467Lys | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/11 | 1463/7672 | 1400/2598 | 467/865 | chr3 | 101758006 | ||
| chr3:101758192
|
T | C | 1 | a0009 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1586T>C | p.Ile529Thr | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/11 | 1649/7672 | 1586/2598 | 529/865 | chr3 | 101758192 | ||
| chr3:101762489
|
C | T | 1 | a0007 | 1 | HG02027.hp1 | stop_gained | HIGH | c.1822C>T | p.Arg608* | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/11 | 1885/7672 | 1822/2598 | 608/865 | chr3 | 101762489 | ||
| chr3:101765507
|
T | C | 1 | a0008 | 1 | NA19080.hp2 | missense_variant | MODERATE | c.2554T>C | p.Cys852Arg | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 2617/7672 | 2554/2598 | 852/865 | chr3 | 101765507 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:101732616
|
C | G | 1 | a0001c0015 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.690C>G | p.Leu230Leu | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/11 | 753/7672 | 690/2598 | 230/865 | chr3 | 101732616 | ||
| chr3:101732616
|
C | T | 1 | a0001c0016 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.690C>T | p.Leu230Leu | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/11 | 753/7672 | 690/2598 | 230/865 | chr3 | 101732616 | ||
| chr3:101755481
|
T | A | 1 | a0001c0008 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.780T>A | p.Pro260Pro | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 7/11 | 843/7672 | 780/2598 | 260/865 | chr3 | 101755481 | ||
| chr3:101764975
|
C | T | 1 | a0001c0013 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.2022C>T | p.Ser674Ser | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 2085/7672 | 2022/2598 | 674/865 | chr3 | 101764975 | ||
| chr3:101765491
|
G | A | 16 | a0001c0001a0001c0008a0001c0013others(13): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(314): Show |
synonymous_variant | LOW | c.2538G>A | p.Gln846Gln | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 2601/7672 | 2538/2598 | 846/865 | chr3 | 101765491 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:101724617
|
T | C | 45 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(42): Show | 347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
5_prime_UTR_variant | MODIFIER | c.-60T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/11 | 60 | chr3 | 101724617 | |||||
| chr3:101765688
|
A | G | 1 | a0001c0001t0032 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*137A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 137 | chr3 | 101765688 | |||||
| chr3:101766434
|
T | C | 1 | a0001c0001t0016 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*883T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 883 | chr3 | 101766434 | |||||
| chr3:101766638
|
G | GAT | 6 | a0001c0001t0004a0001c0001t0006a0001c0001t0014others(3): Show | 31 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1106_*1107dupAT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 1108 | INFO_REALIGN_3_PRIME | chr3 | 101766638 | ||||
| chr3:101766638
|
G | GATAT | 3 | a0001c0001t0007a0001c0001t0010a0001c0001t0013 | 11 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1104_*1107dupATAT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 1108 | INFO_REALIGN_3_PRIME | chr3 | 101766638 | ||||
| chr3:101766639
|
A | T | 1 | a0001c0001t0031 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1088A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 1088 | chr3 | 101766639 | |||||
| chr3:101766805
|
G | A | 1 | a0001c0001t0019 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1254G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 1254 | chr3 | 101766805 | |||||
| chr3:101766924
|
G | A | 1 | a0001c0013t0020 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1373G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 1373 | chr3 | 101766924 | |||||
| chr3:101767160
|
C | T | 1 | a0001c0001t0030 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1609C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 1609 | chr3 | 101767160 | |||||
| chr3:101767206
|
A | G | 3 | a0001c0002t0003a0001c0002t0028a0001c0016t0029 | 24 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1655A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 1655 | chr3 | 101767206 | |||||
| chr3:101767414
|
G | A | 1 | a0001c0001t0021 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1863G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 1863 | chr3 | 101767414 | |||||
| chr3:101767900
|
G | C | 1 | a0001c0001t0015 | 2 | HG03130.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2349G>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 2349 | chr3 | 101767900 | |||||
| chr3:101768076
|
A | T | 8 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(5): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*2525A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 2525 | chr3 | 101768076 | |||||
| chr3:101768650
|
A | G | 1 | a0001c0001t0013 | 2 | HG01884.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3099A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 3099 | chr3 | 101768650 | |||||
| chr3:101768682
|
T | A | 42 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(39): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
3_prime_UTR_variant | MODIFIER | c.*3131T>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 3131 | chr3 | 101768682 | |||||
| chr3:101768732
|
A | C | 1 | a0001c0001t0026 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3181A>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 3181 | chr3 | 101768732 | |||||
| chr3:101769087
|
G | C | 3 | a0001c0001t0005a0001c0001t0022a0001c0001t0030 | 14 | HG00558.hp2 HG02074.hp1 HG02523.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3536G>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 3536 | chr3 | 101769087 | |||||
| chr3:101769163
|
C | T | 1 | a0001c0001t0007 | 6 | HG02145.hp2 HG02615.hp2 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3612C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 3612 | chr3 | 101769163 | |||||
| chr3:101769194
|
A | G | 1 | a0001c0001t0027 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3643A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 3643 | chr3 | 101769194 | |||||
| chr3:101769239
|
C | T | 1 | a0001c0001t0025 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3688C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 3688 | chr3 | 101769239 | |||||
| chr3:101769327
|
G | GT | 3 | a0001c0001t0011a0001c0001t0014a0001c0002t0028 | 6 | HG02135.hp1 HG03098.hp2 NA18943.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3792dupT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 3793 | INFO_REALIGN_3_PRIME | chr3 | 101769327 | ||||
| chr3:101769337
|
T | A | 8 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(5): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*3786T>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 3786 | chr3 | 101769337 | |||||
| chr3:101769345
|
G | A | 1 | a0001c0001t0012 | 3 | NA18961.hp2 NA19011.hp1 NA19087.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3794G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 3794 | chr3 | 101769345 | |||||
| chr3:101769443
|
G | A | 1 | a0001c0001t0017 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3892G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 3892 | chr3 | 101769443 | |||||
| chr3:101769911
|
T | C | 1 | a0001c0001t0023 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4360T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 4360 | chr3 | 101769911 | |||||
| chr3:101770058
|
C | G | 1 | a0001c0001t0022 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4507C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 4507 | chr3 | 101770058 | |||||
| chr3:101770232
|
C | T | 1 | a0001c0001t0024 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4681C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 4681 | chr3 | 101770232 | |||||
| chr3:101770370
|
A | C | 1 | a0001c0001t0017 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4819A>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 11/11 | 4819 | chr3 | 101770370 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:101724847
|
C | T | 4 | a0001c0001t0002g0025a0001c0001t0002g0314a0001c0001t0002g0315others(1): Show | 5 | HG01975.hp2 HG02922.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+128C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | chr3 | 101724847 | ||||||
| chr3:101724940
|
CCAGAAGC others(29): Show |
C | 1 | a0001c0001t0001g0313 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.43+223_43+258delAG others(34): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 101724940 | |||||
| chr3:101725176
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.43+457C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | chr3 | 101725176 | ||||||
| chr3:101725179
|
G | A | 72 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0027others(69): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.43+460G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | chr3 | 101725179 | ||||||
| chr3:101725451
|
T | G | 1 | a0001c0001t0004g0026 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.43+732T>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | chr3 | 101725451 | ||||||
| chr3:101725513
|
C | G | 1 | a0001c0001t0002g0311 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.43+794C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | chr3 | 101725513 | ||||||
| chr3:101725534
|
C | T | 1 | a0001c0001t0002g0310 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.43+815C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | chr3 | 101725534 | ||||||
| chr3:101725538
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.43+819G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | chr3 | 101725538 | ||||||
| chr3:101725663
|
A | T | 1 | a0001c0001t0010g0309 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.44-931A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | chr3 | 101725663 | ||||||
| chr3:101725730
|
G | C | 8 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(5): Show | 8 | HG02698.hp2 HG02735.hp1 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-864G>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | chr3 | 101725730 | ||||||
| chr3:101725805
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.44-789C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | chr3 | 101725805 | ||||||
| chr3:101725877
|
G | GT | 76 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(73): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.44-706dupT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 101725877 | |||||
| chr3:101725877
|
G | T | 1 | a0001c0001t0001g0313 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.44-717G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | chr3 | 101725877 | ||||||
| chr3:101725940
|
C | G | 1 | a0001c0002t0003g0303 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.44-654C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | chr3 | 101725940 | ||||||
| chr3:101726030
|
C | T | 3 | a0001c0001t0012g0300a0001c0001t0012g0301a0001c0001t0012g0302 | 3 | NA18961.hp2 NA19011.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.44-564C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | chr3 | 101726030 | ||||||
| chr3:101726042
|
A | G | 1 | a0001c0001t0005g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.44-552A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | chr3 | 101726042 | ||||||
| chr3:101726274
|
A | G | 101 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0022others(98): Show | 103 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.44-320A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | chr3 | 101726274 | ||||||
| chr3:101726282
|
A | G | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(93): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.44-312A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | chr3 | 101726282 | ||||||
| chr3:101726300
|
C | G | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.44-294C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | chr3 | 101726300 | ||||||
| chr3:101726581
|
G | A | 1 | a0001c0001t0023g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.44-13G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 1/10 | chr3 | 101726581 | ||||||
| chr3:101726894
|
G | A | 1 | a0001c0001t0010g0309 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.186+158G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 2/10 | chr3 | 101726894 | ||||||
| chr3:101727002
|
G | A | 3 | a0001c0001t0002g0016a0001c0001t0002g0145a0001c0001t0002g0146 | 4 | HG00673.hp2 HG02015.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.186+266G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 2/10 | chr3 | 101727002 | ||||||
| chr3:101727056
|
A | G | 4 | a0001c0001t0006g0020a0001c0001t0006g0216a0001c0001t0006g0217others(1): Show | 5 | HG02055.hp2 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.186+320A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 2/10 | chr3 | 101727056 | ||||||
| chr3:101727327
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.187-56G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 2/10 | chr3 | 101727327 | ||||||
| chr3:101727363
|
AAT | A | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(93): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.187-17_187-16delAT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 101727363 | |||||
| chr3:101727587
|
A | T | 8 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(5): Show | 8 | HG02698.hp2 HG02735.hp1 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.345+46A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 3/10 | chr3 | 101727587 | ||||||
| chr3:101727708
|
A | G | 5 | a0001c0001t0002g0215a0001c0001t0006g0020a0001c0001t0006g0216others(2): Show | 6 | HG02055.hp2 HG02965.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.345+167A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 3/10 | chr3 | 101727708 | ||||||
| chr3:101727936
|
T | C | 1 | a0001c0016t0029g0104 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.345+395T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 3/10 | chr3 | 101727936 | ||||||
| chr3:101727939
|
G | T | 21 | a0001c0001t0001g0074a0001c0001t0001g0078a0001c0001t0001g0079others(18): Show | 21 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.345+398G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 3/10 | chr3 | 101727939 | ||||||
| chr3:101727995
|
T | C | 4 | a0001c0001t0002g0005a0001c0001t0002g0147a0001c0001t0002g0148others(1): Show | 6 | NA18939.hp1 NA18941.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.345+454T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 3/10 | chr3 | 101727995 | ||||||
| chr3:101728070
|
C | T | 2 | a0001c0001t0011g0143a0009c0011t0001g0142 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.345+529C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 3/10 | chr3 | 101728070 | ||||||
| chr3:101728262
|
G | GT | 24 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(21): Show | 28 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.346-558dupT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 101728262 | |||||
| chr3:101728262
|
GT | G | 105 | a0001c0001t0001g0108a0001c0001t0002g0001a0001c0001t0002g0002others(102): Show | 125 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.346-558delT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr3 | 101728262 | |||||
| chr3:101728269
|
T | C | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.346-567T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 3/10 | chr3 | 101728269 | ||||||
| chr3:101728269
|
T | G | 3 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222 | 3 | NA18942.hp2 NA18949.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.346-567T>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 3/10 | chr3 | 101728269 | ||||||
| chr3:101728275
|
T | G | 9 | a0001c0001t0001g0021a0001c0001t0001g0223a0001c0001t0001g0224others(6): Show | 10 | HG02155.hp1 NA18612.hp2 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.346-561T>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 3/10 | chr3 | 101728275 | ||||||
| chr3:101728461
|
G | A | 15 | a0001c0002t0003g0004a0001c0002t0003g0014a0001c0002t0003g0015others(12): Show | 19 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.346-375G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 3/10 | chr3 | 101728461 | ||||||
| chr3:101728542
|
G | T | 73 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0027others(70): Show | 76 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.346-294G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 3/10 | chr3 | 101728542 | ||||||
| chr3:101728556
|
G | A | 6 | a0001c0001t0002g0017a0001c0001t0002g0150a0001c0001t0002g0151others(3): Show | 7 | HG00621.hp1 HG02004.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.346-280G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 3/10 | chr3 | 101728556 | ||||||
| chr3:101728639
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.346-197A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 3/10 | chr3 | 101728639 | ||||||
| chr3:101729337
|
C | CA | 15 | a0001c0001t0001g0108a0001c0001t0001g0313a0001c0001t0004g0013others(12): Show | 17 | HG01884.hp2 HG01943.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.447+413dupA | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 101729337 | |||||
| chr3:101729337
|
CA | C | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(93): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.447+413delA | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 101729337 | |||||
| chr3:101729400
|
G | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | NA18987.hp1 NA18993.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.447+463G>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | chr3 | 101729400 | ||||||
| chr3:101729653
|
G | A | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.447+716G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | chr3 | 101729653 | ||||||
| chr3:101729815
|
A | AGCAGTGG others(35): Show |
5 | a0001c0001t0002g0006a0001c0001t0002g0156a0001c0001t0002g0157others(2): Show | 7 | NA18747.hp1 NA18943.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.447+909_447+950dup others(42): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 101729815 | |||||
| chr3:101729965
|
T | C | 1 | a0001c0001t0002g0150 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.447+1028T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | chr3 | 101729965 | ||||||
| chr3:101730228
|
G | GTTGTT | 36 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0057others(33): Show | 38 | HG00140.hp2 HG00558.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.447+1293_447+1294i others(7): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 101730228 | |||||
| chr3:101730228
|
G | GTTGTTTT others(3): Show |
1 | a0001c0001t0004g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.447+1293_447+1294i others(12): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 101730228 | |||||
| chr3:101730228
|
GTTTTTTT others(3): Show |
G | 2 | a0001c0001t0001g0030a0001c0001t0001g0115 | 2 | HG01257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.447+1294_447+1303d others(12): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 101730228 | |||||
| chr3:101730231
|
T | G | 70 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0027others(67): Show | 73 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.447+1294T>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | chr3 | 101730231 | ||||||
| chr3:101730231
|
T | TTTTTG | 19 | a0001c0001t0001g0024a0001c0001t0001g0283a0001c0001t0001g0285others(16): Show | 19 | HG00621.hp2 HG00733.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.447+1342_447+1346d others(7): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 101730231 | |||||
| chr3:101730231
|
T | TTTTTGTT others(3): Show |
2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG01123.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.447+1337_447+1346d others(12): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 101730231 | |||||
| chr3:101730231
|
TTTTTG | T | 30 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(27): Show | 34 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.447+1342_447+1346d others(7): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 101730231 | |||||
| chr3:101730231
|
TTTTTGTT others(3): Show |
T | 13 | a0001c0001t0001g0234a0001c0001t0002g0025a0001c0001t0002g0207others(10): Show | 14 | HG00423.hp1 HG01433.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.447+1337_447+1346d others(12): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 101730231 | |||||
| chr3:101730231
|
TTTTTGTT others(8): Show |
T | 91 | a0001c0001t0001g0232a0001c0001t0002g0001a0001c0001t0002g0002others(88): Show | 108 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.447+1332_447+1346d others(17): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 101730231 | |||||
| chr3:101730231
|
TTTTTGTT others(13): Show |
T | 14 | a0001c0001t0001g0108a0001c0001t0002g0310a0001c0001t0004g0013others(11): Show | 16 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.447+1327_447+1346d others(22): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 101730231 | |||||
| chr3:101730391
|
G | A | 5 | a0001c0001t0007g0012a0001c0001t0007g0105a0001c0001t0007g0106others(2): Show | 6 | HG02145.hp2 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.448-1449G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | chr3 | 101730391 | ||||||
| chr3:101730574
|
A | AT | 100 | a0001c0001t0001g0102a0001c0001t0001g0280a0001c0001t0001g0281others(97): Show | 118 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.448-1249dupT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 101730574 | |||||
| chr3:101730574
|
A | ATT | 7 | a0001c0001t0001g0313a0001c0001t0002g0155a0001c0001t0002g0159others(4): Show | 7 | HG03579.hp2 HG04115.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.448-1250_448-1249d others(4): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 101730574 | |||||
| chr3:101730574
|
AT | A | 70 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0027others(67): Show | 73 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.448-1249delT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 101730574 | |||||
| chr3:101730633
|
A | G | 1 | a0001c0001t0005g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.448-1207A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | chr3 | 101730633 | ||||||
| chr3:101730712
|
A | G | 13 | a0001c0001t0005g0011a0001c0001t0005g0056a0001c0001t0005g0061others(10): Show | 14 | HG00558.hp2 HG02074.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.448-1128A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | chr3 | 101730712 | ||||||
| chr3:101730750
|
G | A | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.448-1090G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | chr3 | 101730750 | ||||||
| chr3:101730889
|
T | A | 292 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(289): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.448-951T>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | chr3 | 101730889 | ||||||
| chr3:101730945
|
A | C | 5 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0121others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.448-895A>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | chr3 | 101730945 | ||||||
| chr3:101730955
|
A | AT | 8 | a0001c0001t0001g0298a0001c0001t0001g0313a0001c0001t0002g0202others(5): Show | 8 | HG01169.hp2 HG01192.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.448-868dupT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 101730955 | |||||
| chr3:101730956
|
T | G | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG02040.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.448-884T>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | chr3 | 101730956 | ||||||
| chr3:101730981
|
A | G | 1 | a0001c0001t0014g0071 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.448-859A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | chr3 | 101730981 | ||||||
| chr3:101731192
|
C | CT | 15 | a0001c0001t0001g0108a0001c0001t0001g0298a0001c0001t0007g0012others(12): Show | 16 | HG01884.hp2 HG02486.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.448-628dupT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 101731192 | |||||
| chr3:101731192
|
CT | C | 141 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(138): Show | 159 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.448-628delT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 101731192 | |||||
| chr3:101731192
|
CTT | C | 7 | a0001c0001t0001g0245a0001c0001t0002g0147a0001c0001t0002g0156others(4): Show | 7 | HG00558.hp1 HG00738.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.448-629_448-628del others(2): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 101731192 | |||||
| chr3:101731250
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.448-590G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | chr3 | 101731250 | ||||||
| chr3:101731285
|
C | T | 1 | a0001c0002t0003g0136 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.448-555C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | chr3 | 101731285 | ||||||
| chr3:101731322
|
T | C | 1 | a0001c0001t0001g0298 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.448-518T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | chr3 | 101731322 | ||||||
| chr3:101731323
|
C | T | 1 | a0001c0001t0001g0298 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.448-517C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | chr3 | 101731323 | ||||||
| chr3:101731414
|
C | T | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(83): Show | 102 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.448-426C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | chr3 | 101731414 | ||||||
| chr3:101731609
|
T | C | 1 | a0001c0001t0002g0151 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.448-231T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 4/10 | chr3 | 101731609 | ||||||
| chr3:101731995
|
A | T | 1 | a0001c0001t0015g0279 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.561+42A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 5/10 | chr3 | 101731995 | ||||||
| chr3:101732192
|
A | G | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | NA18961.hp1 NA18962.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.561+239A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 5/10 | chr3 | 101732192 | ||||||
| chr3:101732211
|
A | G | 13 | a0001c0001t0001g0108a0001c0001t0004g0013a0001c0001t0004g0304others(10): Show | 15 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.561+258A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 5/10 | chr3 | 101732211 | ||||||
| chr3:101732846
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.728+192C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101732846 | ||||||
| chr3:101732958
|
C | CA | 101 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0121others(98): Show | 118 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.728+319dupA | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101732958 | |||||
| chr3:101733126
|
A | T | 1 | a0001c0001t0001g0278 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.728+472A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101733126 | ||||||
| chr3:101733185
|
A | G | 3 | a0001c0001t0001g0053a0001c0001t0021g0052a0007c0014t0001g0051 | 3 | HG02027.hp1 HG02071.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.728+531A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101733185 | ||||||
| chr3:101733391
|
A | G | 15 | a0001c0002t0003g0004a0001c0002t0003g0014a0001c0002t0003g0015others(12): Show | 19 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.728+737A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101733391 | ||||||
| chr3:101733524
|
A | T | 1 | a0001c0001t0001g0298 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.728+870A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101733524 | ||||||
| chr3:101733561
|
C | T | 100 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0022others(97): Show | 102 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.728+907C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101733561 | ||||||
| chr3:101733623
|
C | T | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.728+969C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101733623 | ||||||
| chr3:101733625
|
G | T | 5 | a0001c0001t0007g0012a0001c0001t0007g0105a0001c0001t0007g0106others(2): Show | 6 | HG02145.hp2 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.728+971G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101733625 | ||||||
| chr3:101733626
|
G | A | 5 | a0001c0001t0007g0012a0001c0001t0007g0105a0001c0001t0007g0106others(2): Show | 6 | HG02145.hp2 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.728+972G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101733626 | ||||||
| chr3:101733630
|
A | T | 5 | a0001c0001t0007g0012a0001c0001t0007g0105a0001c0001t0007g0106others(2): Show | 6 | HG02145.hp2 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.728+976A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101733630 | ||||||
| chr3:101733631
|
C | G | 5 | a0001c0001t0007g0012a0001c0001t0007g0105a0001c0001t0007g0106others(2): Show | 6 | HG02145.hp2 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.728+977C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101733631 | ||||||
| chr3:101733675
|
C | T | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.728+1021C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101733675 | ||||||
| chr3:101733688
|
G | A | 13 | a0001c0001t0001g0108a0001c0001t0004g0013a0001c0001t0004g0304others(10): Show | 15 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.728+1034G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101733688 | ||||||
| chr3:101733696
|
A | T | 4 | a0001c0001t0004g0073a0001c0001t0004g0088a0001c0001t0004g0089others(1): Show | 4 | NA18959.hp2 NA18964.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.728+1042A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101733696 | ||||||
| chr3:101733740
|
C | T | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.728+1086C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101733740 | ||||||
| chr3:101733742
|
G | A | 1 | a0001c0013t0020g0307 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.728+1088G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101733742 | ||||||
| chr3:101733743
|
T | G | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(93): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.728+1089T>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101733743 | ||||||
| chr3:101733778
|
C | G | 1 | a0001c0001t0001g0298 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.728+1124C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101733778 | ||||||
| chr3:101733869
|
C | T | 1 | a0001c0001t0002g0198 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.728+1215C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101733869 | ||||||
| chr3:101734511
|
C | T | 1 | a0001c0001t0002g0207 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.728+1857C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101734511 | ||||||
| chr3:101734569
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.728+1915G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101734569 | ||||||
| chr3:101734701
|
C | T | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG00423.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.728+2047C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101734701 | ||||||
| chr3:101734899
|
C | T | 4 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0121others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.728+2245C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101734899 | ||||||
| chr3:101735014
|
C | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(93): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.728+2360C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101735014 | ||||||
| chr3:101735026
|
G | A | 4 | a0001c0002t0003g0004a0001c0002t0003g0014a0001c0002t0003g0128others(1): Show | 7 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.728+2372G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101735026 | ||||||
| chr3:101735114
|
T | G | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.728+2460T>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101735114 | ||||||
| chr3:101735131
|
A | C | 3 | a0001c0002t0003g0135a0001c0002t0003g0137a0001c0002t0028g0138 | 3 | HG02886.hp1 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.728+2477A>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101735131 | ||||||
| chr3:101735147
|
A | G | 15 | a0001c0002t0003g0004a0001c0002t0003g0014a0001c0002t0003g0015others(12): Show | 19 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.728+2493A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101735147 | ||||||
| chr3:101735296
|
C | G | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.728+2642C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101735296 | ||||||
| chr3:101735541
|
A | G | 292 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(289): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.728+2887A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101735541 | ||||||
| chr3:101735627
|
C | T | 11 | a0001c0001t0001g0108a0001c0001t0007g0012a0001c0001t0007g0105others(8): Show | 12 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.728+2973C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101735627 | ||||||
| chr3:101735670
|
A | T | 292 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(289): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.728+3016A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101735670 | ||||||
| chr3:101735862
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.728+3208G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101735862 | ||||||
| chr3:101735940
|
A | ACACAGGG others(3): Show |
1 | a0001c0001t0001g0298 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.728+3287_728+3296d others(12): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101735940 | |||||
| chr3:101736074
|
C | G | 1 | a0001c0001t0004g0050 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.728+3420C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101736074 | ||||||
| chr3:101736079
|
G | T | 1 | a0001c0001t0002g0156 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.728+3425G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101736079 | ||||||
| chr3:101736376
|
G | A | 3 | a0001c0001t0002g0164a0001c0001t0002g0165a0004c0004t0002g0018 | 4 | NA18939.hp2 NA18950.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.728+3722G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101736376 | ||||||
| chr3:101736430
|
A | C | 1 | a0001c0001t0023g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.728+3776A>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101736430 | ||||||
| chr3:101736454
|
G | A | 1 | a0001c0001t0005g0061 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.728+3800G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101736454 | ||||||
| chr3:101736848
|
T | A | 1 | a0001c0001t0001g0243 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.728+4194T>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101736848 | ||||||
| chr3:101737063
|
G | A | 71 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0027others(68): Show | 74 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.728+4409G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101737063 | ||||||
| chr3:101737122
|
T | C | 110 | a0001c0001t0001g0108a0001c0001t0002g0001a0001c0001t0002g0002others(107): Show | 130 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.728+4468T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101737122 | ||||||
| chr3:101737290
|
C | T | 2 | a0001c0001t0011g0143a0009c0011t0001g0142 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.728+4636C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101737290 | ||||||
| chr3:101737291
|
G | A | 13 | a0001c0001t0001g0108a0001c0001t0004g0013a0001c0001t0004g0304others(10): Show | 15 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.728+4637G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101737291 | ||||||
| chr3:101737384
|
A | G | 1 | a0001c0001t0002g0197 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.728+4730A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101737384 | ||||||
| chr3:101737529
|
C | T | 4 | a0001c0001t0002g0005a0001c0001t0002g0147a0001c0001t0002g0148others(1): Show | 6 | NA18939.hp1 NA18941.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.728+4875C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101737529 | ||||||
| chr3:101737840
|
A | G | 72 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(69): Show | 88 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.728+5186A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101737840 | ||||||
| chr3:101737844
|
T | G | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.728+5190T>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101737844 | ||||||
| chr3:101737908
|
A | T | 4 | a0001c0001t0006g0020a0001c0001t0006g0216a0001c0001t0006g0217others(1): Show | 5 | HG02055.hp2 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.728+5254A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101737908 | ||||||
| chr3:101738011
|
C | CA | 117 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0022others(114): Show | 124 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.728+5380dupA | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101738011 | |||||
| chr3:101738011
|
C | CAA | 31 | a0001c0001t0001g0024a0001c0001t0001g0094a0001c0001t0001g0123others(28): Show | 32 | HG00423.hp2 HG00609.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.728+5379_728+5380d others(4): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101738011 | |||||
| chr3:101738011
|
CA | C | 47 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(44): Show | 50 | HG00544.hp2 HG00558.hp2 HG01175.hp1 others(47): Show |
intron_variant | MODIFIER | c.728+5380delA | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101738011 | |||||
| chr3:101738029
|
A | G | 4 | a0001c0001t0006g0020a0001c0001t0006g0216a0001c0001t0006g0217others(1): Show | 5 | HG02055.hp2 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.728+5375A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101738029 | ||||||
| chr3:101738292
|
A | C | 1 | a0001c0001t0001g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.728+5638A>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101738292 | ||||||
| chr3:101738340
|
C | T | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.728+5686C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101738340 | ||||||
| chr3:101738372
|
A | C | 1 | a0001c0001t0001g0095 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.728+5718A>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101738372 | ||||||
| chr3:101738391
|
C | T | 3 | a0001c0001t0001g0227a0001c0001t0001g0229a0001c0001t0001g0230 | 3 | NA18946.hp1 NA18947.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.728+5737C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101738391 | ||||||
| chr3:101738547
|
C | A | 292 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(289): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.728+5893C>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101738547 | ||||||
| chr3:101738556
|
C | T | 5 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0121others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.728+5902C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101738556 | ||||||
| chr3:101738588
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.728+5934C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101738588 | ||||||
| chr3:101738669
|
G | T | 1 | a0001c0001t0002g0156 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.728+6015G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101738669 | ||||||
| chr3:101738753
|
C | T | 1 | a0001c0001t0002g0146 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.728+6099C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101738753 | ||||||
| chr3:101738937
|
A | T | 1 | a0001c0001t0001g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.728+6283A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101738937 | ||||||
| chr3:101739451
|
C | G | 1 | a0001c0002t0003g0130 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.728+6797C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101739451 | ||||||
| chr3:101739618
|
A | G | 6 | a0001c0002t0008g0116a0001c0002t0008g0117a0001c0002t0008g0119others(3): Show | 6 | HG01433.hp2 HG02698.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.728+6964A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101739618 | ||||||
| chr3:101739636
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.728+6982A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101739636 | ||||||
| chr3:101739903
|
T | TA | 14 | a0001c0001t0001g0108a0001c0001t0001g0313a0001c0001t0004g0013others(11): Show | 16 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.728+7263dupA | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101739903 | |||||
| chr3:101739903
|
T | TAA | 95 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(92): Show | 113 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.728+7262_728+7263d others(4): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101739903 | |||||
| chr3:101739921
|
G | A | 320 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(317): Show | 351 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.728+7267G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101739921 | ||||||
| chr3:101740099
|
A | C | 1 | a0001c0001t0001g0072 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.728+7445A>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101740099 | ||||||
| chr3:101740126
|
G | A | 13 | a0001c0001t0001g0108a0001c0001t0004g0013a0001c0001t0004g0304others(10): Show | 15 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.728+7472G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101740126 | ||||||
| chr3:101740129
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.728+7475A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101740129 | ||||||
| chr3:101740244
|
A | G | 13 | a0001c0001t0001g0108a0001c0001t0004g0013a0001c0001t0004g0304others(10): Show | 15 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.728+7590A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101740244 | ||||||
| chr3:101740691
|
G | A | 2 | a0001c0001t0011g0143a0009c0011t0001g0142 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.728+8037G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101740691 | ||||||
| chr3:101740801
|
C | G | 7 | a0001c0001t0002g0173a0001c0001t0002g0192a0001c0001t0002g0193others(4): Show | 7 | HG00609.hp2 NA18944.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.728+8147C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101740801 | ||||||
| chr3:101741049
|
CAG | C | 13 | a0001c0001t0001g0108a0001c0001t0004g0013a0001c0001t0004g0304others(10): Show | 15 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.728+8396_728+8397d others(4): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101741049 | ||||||
| chr3:101741056
|
G | C | 10 | a0001c0001t0001g0008a0001c0001t0001g0232a0001c0001t0001g0236others(7): Show | 11 | HG00673.hp1 HG02083.hp2 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.728+8402G>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101741056 | ||||||
| chr3:101741059
|
C | T | 1 | a0001c0001t0004g0090 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.728+8405C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101741059 | ||||||
| chr3:101741222
|
A | C | 1 | a0001c0002t0003g0127 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.728+8568A>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101741222 | ||||||
| chr3:101741299
|
A | G | 1 | a0001c0001t0027g0204 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.728+8645A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101741299 | ||||||
| chr3:101741490
|
A | G | 4 | a0001c0001t0001g0250a0001c0001t0001g0265a0001c0001t0001g0266others(1): Show | 4 | HG02040.hp1 HG02071.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.728+8836A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101741490 | ||||||
| chr3:101741529
|
A | G | 190 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0027others(187): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.728+8875A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101741529 | ||||||
| chr3:101741651
|
A | G | 101 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0022others(98): Show | 104 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.728+8997A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101741651 | ||||||
| chr3:101741652
|
T | C | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.728+8998T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101741652 | ||||||
| chr3:101741655
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0115 | 2 | HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.728+9001A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101741655 | ||||||
| chr3:101741709
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.728+9055G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101741709 | ||||||
| chr3:101741808
|
G | A | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(93): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.728+9154G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101741808 | ||||||
| chr3:101741899
|
A | G | 95 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(92): Show | 113 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.728+9245A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101741899 | ||||||
| chr3:101741911
|
G | A | 1 | a0001c0013t0020g0307 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.728+9257G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101741911 | ||||||
| chr3:101741912
|
C | T | 3 | a0001c0001t0006g0216a0001c0001t0006g0217a0001c0001t0006g0218 | 3 | HG02055.hp2 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.728+9258C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101741912 | ||||||
| chr3:101741984
|
G | A | 1 | a0001c0001t0026g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.728+9330G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101741984 | ||||||
| chr3:101742041
|
C | CA | 25 | a0001c0001t0001g0079a0001c0001t0001g0096a0001c0001t0001g0246others(22): Show | 27 | HG00323.hp1 HG00609.hp1 HG01928.hp2 others(24): Show |
intron_variant | MODIFIER | c.728+9400dupA | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101742041 | |||||
| chr3:101742054
|
A | AAC | 6 | a0001c0001t0002g0157a0001c0001t0002g0166a0001c0001t0002g0167others(3): Show | 6 | HG02055.hp1 HG02135.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.728+9400_728+9401i others(4): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101742054 | ||||||
| chr3:101742054
|
A | AC | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(81): Show | 101 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.728+9401dupC | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101742054 | |||||
| chr3:101742054
|
A | C | 1 | a0001c0001t0002g0174 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.728+9400A>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101742054 | ||||||
| chr3:101742240
|
T | C | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.728+9586T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101742240 | ||||||
| chr3:101742333
|
T | C | 110 | a0001c0001t0001g0108a0001c0001t0002g0001a0001c0001t0002g0002others(107): Show | 130 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.728+9679T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101742333 | ||||||
| chr3:101742502
|
AC | A | 318 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(315): Show | 347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.728+9850delC | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101742502 | |||||
| chr3:101742589
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.728+9935G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101742589 | ||||||
| chr3:101742733
|
TA | T | 7 | a0001c0001t0001g0115a0001c0001t0001g0228a0001c0001t0001g0247others(4): Show | 7 | HG00323.hp1 HG00558.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.728+10094delA | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101742733 | |||||
| chr3:101742851
|
A | T | 2 | a0001c0001t0001g0049a0001c0002t0003g0129 | 2 | HG00280.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.728+10197A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101742851 | ||||||
| chr3:101743106
|
T | C | 318 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(315): Show | 347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.728+10452T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101743106 | ||||||
| chr3:101743377
|
C | A | 1 | a0001c0013t0020g0307 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.728+10723C>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101743377 | ||||||
| chr3:101743397
|
T | A | 103 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0022others(100): Show | 106 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.728+10743T>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101743397 | ||||||
| chr3:101743481
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.728+10827C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101743481 | ||||||
| chr3:101743489
|
A | G | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.728+10835A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101743489 | ||||||
| chr3:101743549
|
CTG | C | 6 | a0001c0001t0001g0022a0001c0001t0001g0254a0001c0001t0001g0255others(3): Show | 6 | NA18957.hp1 NA18988.hp2 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.728+10898_728+1089 others(6): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101743549 | |||||
| chr3:101743604
|
C | T | 1 | a0001c0002t0008g0119 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.728+10950C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101743604 | ||||||
| chr3:101743793
|
G | A | 13 | a0001c0001t0001g0108a0001c0001t0004g0013a0001c0001t0004g0304others(10): Show | 15 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.728+11139G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101743793 | ||||||
| chr3:101743808
|
G | T | 1 | a0001c0001t0026g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.728+11154G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101743808 | ||||||
| chr3:101743870
|
C | T | 5 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0121others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.728+11216C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101743870 | ||||||
| chr3:101743871
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.728+11217G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101743871 | ||||||
| chr3:101743945
|
G | A | 13 | a0001c0001t0001g0108a0001c0001t0004g0013a0001c0001t0004g0304others(10): Show | 15 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.728+11291G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101743945 | ||||||
| chr3:101743968
|
A | C | 293 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(290): Show | 319 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(316): Show |
intron_variant | MODIFIER | c.728+11314A>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101743968 | ||||||
| chr3:101744004
|
C | CA | 97 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(94): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.728+11366dupA | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101744004 | |||||
| chr3:101744004
|
CA | C | 14 | a0001c0001t0001g0108a0001c0001t0004g0073a0001c0001t0007g0012others(11): Show | 15 | HG02145.hp2 HG02486.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.728+11366delA | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101744004 | |||||
| chr3:101744058
|
T | C | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.729-11372T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101744058 | ||||||
| chr3:101744153
|
A | G | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.729-11277A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101744153 | ||||||
| chr3:101744155
|
C | A | 1 | a0001c0001t0001g0270 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.729-11275C>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101744155 | ||||||
| chr3:101744216
|
A | G | 1 | a0001c0001t0001g0039 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.729-11214A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101744216 | ||||||
| chr3:101744301
|
A | T | 2 | a0001c0001t0011g0143a0009c0011t0001g0142 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.729-11129A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101744301 | ||||||
| chr3:101744413
|
G | A | 4 | a0001c0001t0002g0310a0001c0001t0012g0300a0001c0001t0012g0301others(1): Show | 4 | NA18961.hp2 NA18966.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.729-11017G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101744413 | ||||||
| chr3:101744463
|
A | G | 1 | a0001c0002t0003g0127 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.729-10967A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101744463 | ||||||
| chr3:101744469
|
G | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(93): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.729-10961G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101744469 | ||||||
| chr3:101744514
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.729-10916C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101744514 | ||||||
| chr3:101744547
|
C | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(93): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.729-10883C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101744547 | ||||||
| chr3:101744583
|
C | CA | 26 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0041others(23): Show | 27 | HG00673.hp1 HG00733.hp2 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.729-10830dupA | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101744583 | |||||
| chr3:101744583
|
CA | C | 6 | a0001c0001t0001g0048a0001c0001t0001g0100a0001c0001t0004g0086others(3): Show | 6 | HG01496.hp2 HG02074.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.729-10830delA | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101744583 | |||||
| chr3:101744597
|
A | C | 4 | a0001c0001t0002g0001a0001c0001t0002g0188a0001c0001t0002g0189others(1): Show | 8 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.729-10833A>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101744597 | ||||||
| chr3:101744600
|
A | T | 1 | a0001c0002t0018g0118 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.729-10830A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101744600 | ||||||
| chr3:101744650
|
G | GA | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(93): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.729-10779dupA | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101744650 | |||||
| chr3:101745014
|
T | C | 2 | a0001c0001t0011g0143a0009c0011t0001g0142 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.729-10416T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101745014 | ||||||
| chr3:101745051
|
C | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(93): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.729-10379C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101745051 | ||||||
| chr3:101745056
|
C | T | 13 | a0001c0001t0001g0108a0001c0001t0004g0013a0001c0001t0004g0304others(10): Show | 15 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.729-10374C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101745056 | ||||||
| chr3:101745146
|
C | T | 2 | a0001c0001t0015g0242a0001c0001t0015g0279 | 2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.729-10284C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101745146 | ||||||
| chr3:101745167
|
A | G | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.729-10263A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101745167 | ||||||
| chr3:101745207
|
A | G | 4 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0121others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.729-10223A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101745207 | ||||||
| chr3:101745572
|
C | T | 4 | a0001c0001t0002g0025a0001c0001t0002g0314a0001c0001t0002g0315others(1): Show | 5 | HG01975.hp2 HG02922.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.729-9858C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101745572 | ||||||
| chr3:101745649
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.729-9781C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101745649 | ||||||
| chr3:101745738
|
T | C | 2 | a0001c0001t0002g0166a0001c0001t0002g0171 | 2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.729-9692T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101745738 | ||||||
| chr3:101745912
|
C | G | 3 | a0001c0001t0001g0108a0001c0001t0013g0109a0001c0001t0013g0110 | 3 | HG01884.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.729-9518C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101745912 | ||||||
| chr3:101745992
|
G | A | 2 | a0001c0001t0004g0013a0001c0001t0004g0304 | 3 | HG02280.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.729-9438G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101745992 | ||||||
| chr3:101746038
|
A | G | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0059others(1): Show | 4 | HG02451.hp2 HG02895.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.729-9392A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746038 | ||||||
| chr3:101746079
|
A | G | 1 | a0001c0001t0026g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.729-9351A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746079 | ||||||
| chr3:101746173
|
G | C | 2 | a0001c0001t0002g0175a0001c0001t0002g0199 | 2 | NA19060.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.729-9257G>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746173 | ||||||
| chr3:101746187
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.729-9243G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746187 | ||||||
| chr3:101746196
|
A | T | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.729-9234A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746196 | ||||||
| chr3:101746292
|
A | T | 2 | a0001c0001t0002g0186a0001c0001t0002g0187 | 2 | HG00140.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.729-9138A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746292 | ||||||
| chr3:101746360
|
C | T | 2 | a0001c0001t0002g0175a0001c0001t0002g0199 | 2 | NA19060.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.729-9070C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746360 | ||||||
| chr3:101746369
|
C | G | 1 | a0001c0001t0001g0239 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.729-9061C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746369 | ||||||
| chr3:101746369
|
C | T | 1 | a0001c0001t0023g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.729-9061C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746369 | ||||||
| chr3:101746370
|
G | C | 1 | a0001c0001t0001g0239 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.729-9060G>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746370 | ||||||
| chr3:101746386
|
T | G | 1 | a0001c0001t0001g0265 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.729-9044T>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746386 | ||||||
| chr3:101746447
|
A | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0047 | 2 | HG01433.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.729-8983A>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746447 | ||||||
| chr3:101746497
|
C | T | 2 | a0001c0001t0011g0143a0009c0011t0001g0142 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.729-8933C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746497 | ||||||
| chr3:101746574
|
C | G | 13 | a0001c0001t0001g0108a0001c0001t0004g0013a0001c0001t0004g0304others(10): Show | 15 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.729-8856C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746574 | ||||||
| chr3:101746671
|
G | T | 1 | a0001c0001t0001g0241 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.729-8759G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746671 | ||||||
| chr3:101746699
|
C | G | 1 | a0001c0001t0006g0218 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.729-8731C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746699 | ||||||
| chr3:101746815
|
C | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(93): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.729-8615C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746815 | ||||||
| chr3:101746816
|
T | G | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(93): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.729-8614T>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746816 | ||||||
| chr3:101746873
|
T | C | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.729-8557T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746873 | ||||||
| chr3:101746937
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0255 | 2 | NA18945.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.729-8493A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746937 | ||||||
| chr3:101746985
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.729-8445T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101746985 | ||||||
| chr3:101747091
|
C | T | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.729-8339C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101747091 | ||||||
| chr3:101747122
|
G | A | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.729-8308G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101747122 | ||||||
| chr3:101747122
|
G | C | 1 | a0001c0001t0001g0255 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.729-8308G>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101747122 | ||||||
| chr3:101747133
|
A | G | 312 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(309): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.729-8297A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101747133 | ||||||
| chr3:101747146
|
A | T | 2 | a0001c0001t0015g0242a0001c0001t0015g0279 | 2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.729-8284A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101747146 | ||||||
| chr3:101747151
|
A | C | 73 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0027others(70): Show | 76 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.729-8279A>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101747151 | ||||||
| chr3:101747161
|
C | T | 112 | a0001c0001t0001g0108a0001c0001t0002g0001a0001c0001t0002g0002others(109): Show | 132 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.729-8269C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101747161 | ||||||
| chr3:101747258
|
C | CT | 17 | a0001c0001t0001g0009a0001c0001t0001g0046a0001c0001t0001g0224others(14): Show | 18 | HG00735.hp1 HG01099.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.729-8153dupT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101747258 | |||||
| chr3:101747258
|
CT | C | 91 | a0001c0001t0001g0049a0001c0001t0001g0074a0001c0001t0002g0001others(88): Show | 109 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.729-8153delT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101747258 | |||||
| chr3:101747352
|
C | A | 1 | a0001c0002t0003g0127 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.729-8078C>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101747352 | ||||||
| chr3:101747372
|
G | A | 1 | a0001c0002t0008g0116 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.729-8058G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101747372 | ||||||
| chr3:101747562
|
C | CT | 17 | a0001c0001t0001g0239a0001c0001t0001g0273a0001c0002t0003g0004others(14): Show | 21 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.729-7855dupT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101747562 | |||||
| chr3:101747620
|
G | A | 1 | a0001c0001t0026g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.729-7810G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101747620 | ||||||
| chr3:101747625
|
C | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(93): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.729-7805C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101747625 | ||||||
| chr3:101747698
|
A | AT | 163 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0027others(160): Show | 184 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.729-7718dupT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101747698 | |||||
| chr3:101747885
|
G | A | 1 | a0001c0002t0008g0116 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.729-7545G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101747885 | ||||||
| chr3:101747946
|
G | T | 8 | a0001c0001t0001g0023a0001c0001t0001g0261a0001c0001t0001g0262others(5): Show | 8 | HG00642.hp1 HG01346.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.729-7484G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101747946 | ||||||
| chr3:101748091
|
C | G | 1 | a0001c0001t0001g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.729-7339C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101748091 | ||||||
| chr3:101748129
|
C | CA | 41 | a0001c0001t0001g0041a0001c0001t0001g0049a0001c0001t0001g0108others(38): Show | 46 | HG00280.hp1 HG00621.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.729-7276dupA | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101748129 | |||||
| chr3:101748129
|
C | CAA | 60 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(57): Show | 64 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.729-7277_729-7276d others(4): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101748129 | |||||
| chr3:101748129
|
C | CAAA | 20 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0034others(17): Show | 20 | HG00140.hp2 HG00544.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.729-7278_729-7276d others(5): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101748129 | |||||
| chr3:101748129
|
C | CAAAA | 8 | a0001c0001t0001g0054a0001c0001t0001g0094a0001c0001t0001g0115others(5): Show | 8 | HG01175.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.729-7279_729-7276d others(6): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101748129 | |||||
| chr3:101748129
|
CA | C | 89 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0022others(86): Show | 93 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.729-7276delA | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101748129 | |||||
| chr3:101748239
|
G | GT | 10 | a0001c0001t0001g0079a0001c0001t0001g0224a0001c0001t0001g0295others(7): Show | 10 | HG01123.hp2 HG01928.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.729-7181dupT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101748239 | |||||
| chr3:101748239
|
G | T | 1 | a0001c0001t0001g0240 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.729-7191G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101748239 | ||||||
| chr3:101748287
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.729-7143A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101748287 | ||||||
| chr3:101748369
|
A | C | 1 | a0001c0001t0001g0033 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.729-7061A>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101748369 | ||||||
| chr3:101748395
|
T | G | 73 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0027others(70): Show | 76 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.729-7035T>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101748395 | ||||||
| chr3:101748456
|
C | G | 312 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(309): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.729-6974C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101748456 | ||||||
| chr3:101748701
|
C | T | 102 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0022others(99): Show | 104 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.729-6729C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101748701 | ||||||
| chr3:101748765
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.729-6665C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101748765 | ||||||
| chr3:101748797
|
C | T | 2 | a0001c0001t0011g0143a0009c0011t0001g0142 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.729-6633C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101748797 | ||||||
| chr3:101748891
|
C | T | 37 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0219others(34): Show | 39 | HG00423.hp2 HG00673.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.729-6539C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101748891 | ||||||
| chr3:101748932
|
G | A | 1 | a0001c0001t0019g0260 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.729-6498G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101748932 | ||||||
| chr3:101748939
|
C | T | 3 | a0001c0001t0001g0245a0001c0001t0001g0283a0008c0012t0001g0233 | 3 | HG00558.hp1 HG02027.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.729-6491C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101748939 | ||||||
| chr3:101748941
|
A | T | 5 | a0001c0001t0002g0215a0001c0001t0006g0020a0001c0001t0006g0216others(2): Show | 6 | HG02055.hp2 HG02965.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.729-6489A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101748941 | ||||||
| chr3:101748998
|
T | G | 1 | a0001c0001t0026g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.729-6432T>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101748998 | ||||||
| chr3:101749066
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0033a0001c0001t0001g0058 | 4 | HG01106.hp2 HG02886.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.729-6364C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749066 | ||||||
| chr3:101749082
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.729-6348G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749082 | ||||||
| chr3:101749137
|
C | T | 4 | a0001c0001t0001g0241a0001c0001t0015g0242a0001c0001t0015g0279others(1): Show | 4 | HG00639.hp2 HG03130.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.729-6293C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749137 | ||||||
| chr3:101749143
|
C | A | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.729-6287C>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749143 | ||||||
| chr3:101749145
|
T | TC | 7 | a0001c0001t0001g0028a0001c0001t0001g0262a0001c0001t0001g0285others(4): Show | 7 | HG01496.hp1 HG02055.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.729-6279dupC | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101749145 | |||||
| chr3:101749209
|
T | C | 5 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0121others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.729-6221T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749209 | ||||||
| chr3:101749443
|
T | C | 1 | a0001c0002t0003g0127 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.729-5987T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749443 | ||||||
| chr3:101749473
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.729-5957A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749473 | ||||||
| chr3:101749519
|
T | A | 185 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0027others(182): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.729-5911T>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749519 | ||||||
| chr3:101749565
|
G | A | 3 | a0001c0001t0010g0111a0001c0001t0010g0112a0001c0001t0010g0309 | 3 | HG02486.hp1 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.729-5865G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749565 | ||||||
| chr3:101749610
|
A | G | 281 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(278): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.729-5820A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749610 | ||||||
| chr3:101749749
|
T | C | 101 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0022others(98): Show | 104 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.729-5681T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749749 | ||||||
| chr3:101749759
|
T | A | 1 | a0001c0002t0008g0124 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.729-5671T>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749759 | ||||||
| chr3:101749865
|
G | T | 5 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0121others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.729-5565G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749865 | ||||||
| chr3:101749870
|
A | C | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.729-5560A>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749870 | ||||||
| chr3:101749871
|
G | A | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.729-5559G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749871 | ||||||
| chr3:101749877
|
T | C | 4 | a0001c0001t0006g0020a0001c0001t0006g0216a0001c0001t0006g0217others(1): Show | 5 | HG02055.hp2 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.729-5553T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749877 | ||||||
| chr3:101749907
|
A | G | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.729-5523A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749907 | ||||||
| chr3:101749919
|
T | C | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.729-5511T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749919 | ||||||
| chr3:101749920
|
G | A | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.729-5510G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749920 | ||||||
| chr3:101749953
|
C | G | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.729-5477C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749953 | ||||||
| chr3:101749957
|
G | C | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.729-5473G>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749957 | ||||||
| chr3:101749987
|
C | G | 3 | a0001c0001t0002g0215a0001c0001t0023g0103a0001c0001t0026g0114 | 3 | HG01943.hp1 HG02109.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.729-5443C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749987 | ||||||
| chr3:101750022
|
G | A | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.729-5408G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101750022 | ||||||
| chr3:101750027
|
C | T | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.729-5403C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101750027 | ||||||
| chr3:101750047
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.729-5383G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101750047 | ||||||
| chr3:101750047
|
G | GT | 97 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(94): Show | 115 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.729-5380dupT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101750047 | |||||
| chr3:101750056
|
T | C | 1 | a0001c0001t0004g0304 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.729-5374T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101750056 | ||||||
| chr3:101750134
|
C | T | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.729-5296C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101750134 | ||||||
| chr3:101750378
|
T | C | 1 | a0001c0001t0002g0181 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.729-5052T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101750378 | ||||||
| chr3:101750538
|
G | T | 1 | a0001c0001t0001g0234 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.729-4892G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101750538 | ||||||
| chr3:101750581
|
A | G | 103 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0022others(100): Show | 106 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.729-4849A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101750581 | ||||||
| chr3:101750698
|
G | A | 1 | a0001c0013t0020g0307 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.729-4732G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101750698 | ||||||
| chr3:101750739
|
C | T | 2 | a0001c0001t0011g0143a0009c0011t0001g0142 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.729-4691C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101750739 | ||||||
| chr3:101751164
|
T | G | 1 | a0001c0001t0001g0042 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.729-4266T>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101751164 | ||||||
| chr3:101751219
|
G | A | 2 | a0001c0001t0001g0308a0001c0001t0017g0144 | 2 | HG02083.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.729-4211G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101751219 | ||||||
| chr3:101751392
|
G | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(93): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.729-4038G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101751392 | ||||||
| chr3:101751403
|
G | C | 5 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0121others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.729-4027G>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101751403 | ||||||
| chr3:101751493
|
G | C | 110 | a0001c0001t0001g0108a0001c0001t0002g0001a0001c0001t0002g0002others(107): Show | 130 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.729-3937G>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101751493 | ||||||
| chr3:101751714
|
A | C | 14 | a0001c0001t0001g0024a0001c0001t0001g0285a0001c0001t0001g0286others(11): Show | 14 | HG00733.hp1 HG00735.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.729-3716A>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101751714 | ||||||
| chr3:101751717
|
G | A | 124 | a0001c0001t0001g0024a0001c0001t0001g0108a0001c0001t0001g0285others(121): Show | 144 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.729-3713G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101751717 | ||||||
| chr3:101752068
|
C | A | 1 | a0001c0002t0003g0134 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.729-3362C>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101752068 | ||||||
| chr3:101752140
|
C | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(93): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.729-3290C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101752140 | ||||||
| chr3:101752194
|
T | G | 1 | a0001c0013t0020g0307 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.729-3236T>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101752194 | ||||||
| chr3:101752310
|
C | G | 1 | a0001c0001t0001g0078 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.729-3120C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101752310 | ||||||
| chr3:101752452
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.729-2978A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101752452 | ||||||
| chr3:101752541
|
C | G | 14 | a0001c0002t0003g0004a0001c0002t0003g0015a0001c0002t0003g0128others(11): Show | 17 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.729-2889C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101752541 | ||||||
| chr3:101752648
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0238a0001c0001t0001g0239others(3): Show | 7 | HG02083.hp2 NA18747.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.729-2782C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101752648 | ||||||
| chr3:101752682
|
G | A | 1 | a0001c0001t0026g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.729-2748G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101752682 | ||||||
| chr3:101752714
|
G | A | 3 | a0001c0001t0006g0216a0001c0001t0006g0217a0001c0001t0006g0218 | 3 | HG02055.hp2 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.729-2716G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101752714 | ||||||
| chr3:101752722
|
C | T | 5 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0121others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.729-2708C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101752722 | ||||||
| chr3:101752910
|
C | T | 1 | a0003c0005t0001g0284 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.729-2520C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101752910 | ||||||
| chr3:101752968
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.729-2462C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101752968 | ||||||
| chr3:101753073
|
G | A | 13 | a0001c0001t0001g0108a0001c0001t0004g0013a0001c0001t0004g0304others(10): Show | 15 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.729-2357G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753073 | ||||||
| chr3:101753406
|
G | T | 101 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0022others(98): Show | 103 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.729-2024G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753406 | ||||||
| chr3:101753532
|
C | G | 91 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(88): Show | 108 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.729-1898C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753532 | ||||||
| chr3:101753560
|
G | T | 1 | a0001c0001t0026g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.729-1870G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753560 | ||||||
| chr3:101753592
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.729-1838C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753592 | ||||||
| chr3:101753608
|
C | T | 1 | a0004c0004t0002g0018 | 2 | NA18966.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.729-1822C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753608 | ||||||
| chr3:101753609
|
G | A | 1 | a0001c0001t0021g0052 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.729-1821G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753609 | ||||||
| chr3:101753629
|
T | C | 293 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(290): Show | 319 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(316): Show |
intron_variant | MODIFIER | c.729-1801T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753629 | ||||||
| chr3:101753657
|
G | C | 292 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(289): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.729-1773G>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753657 | ||||||
| chr3:101753749
|
C | T | 13 | a0001c0001t0001g0108a0001c0001t0004g0013a0001c0001t0004g0304others(10): Show | 15 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.729-1681C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753749 | ||||||
| chr3:101753750
|
G | A | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(93): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.729-1680G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753750 | ||||||
| chr3:101753762
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.729-1668C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753762 | ||||||
| chr3:101753785
|
G | A | 11 | a0001c0001t0001g0108a0001c0001t0007g0012a0001c0001t0007g0105others(8): Show | 12 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.729-1645G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753785 | ||||||
| chr3:101753884
|
G | A | 1 | a0001c0001t0007g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.729-1546G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753884 | ||||||
| chr3:101753888
|
T | C | 1 | a0001c0001t0007g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.729-1542T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753888 | ||||||
| chr3:101753889
|
G | A | 1 | a0001c0001t0007g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.729-1541G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753889 | ||||||
| chr3:101753890
|
C | T | 6 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0121others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.729-1540C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753890 | ||||||
| chr3:101753895
|
G | A | 1 | a0001c0001t0007g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.729-1535G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753895 | ||||||
| chr3:101753985
|
A | G | 112 | a0001c0001t0001g0108a0001c0001t0002g0001a0001c0001t0002g0002others(109): Show | 132 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.729-1445A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753985 | ||||||
| chr3:101753997
|
G | A | 1 | a0001c0001t0023g0103 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.729-1433G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753997 | ||||||
| chr3:101754042
|
CT | C | 160 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(157): Show | 165 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.729-1362delT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101754042 | |||||
| chr3:101754042
|
CTT | C | 108 | a0001c0001t0001g0043a0001c0001t0001g0102a0001c0001t0001g0108others(105): Show | 127 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.729-1363_729-1362d others(4): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101754042 | |||||
| chr3:101754042
|
CTTT | C | 13 | a0001c0001t0002g0019a0001c0001t0002g0145a0001c0001t0002g0149others(10): Show | 14 | HG00639.hp1 HG00738.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.729-1364_729-1362d others(5): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101754042 | |||||
| chr3:101754243
|
G | C | 311 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(308): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.729-1187G>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101754243 | ||||||
| chr3:101754243
|
G | T | 1 | a0001c0001t0026g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.729-1187G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101754243 | ||||||
| chr3:101754244
|
G | A | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(93): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.729-1186G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101754244 | ||||||
| chr3:101754623
|
G | A | 3 | a0002c0003t0002g0209a0002c0003t0002g0212a0002c0003t0002g0214 | 3 | HG01243.hp2 HG01884.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.729-807G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101754623 | ||||||
| chr3:101754651
|
A | G | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.729-779A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101754651 | ||||||
| chr3:101754672
|
A | G | 4 | a0001c0001t0002g0025a0001c0001t0002g0314a0001c0001t0002g0315others(1): Show | 5 | HG01975.hp2 HG02922.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.729-758A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101754672 | ||||||
| chr3:101754796
|
G | A | 48 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(45): Show | 49 | HG00323.hp1 HG00558.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.729-634G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101754796 | ||||||
| chr3:101754896
|
A | AT | 108 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0022others(105): Show | 111 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.729-518dupT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101754896 | |||||
| chr3:101754896
|
AT | A | 6 | a0001c0001t0001g0049a0001c0001t0002g0188a0001c0001t0002g0207others(3): Show | 7 | HG00639.hp1 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.729-518delT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 101754896 | |||||
| chr3:101754966
|
C | T | 1 | a0006c0007t0001g0055 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.729-464C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101754966 | ||||||
| chr3:101755047
|
G | T | 1 | a0001c0001t0005g0066 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.729-383G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101755047 | ||||||
| chr3:101755056
|
G | T | 1 | a0001c0001t0007g0107 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.729-374G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101755056 | ||||||
| chr3:101755277
|
G | T | 1 | a0001c0001t0001g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.729-153G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101755277 | ||||||
| chr3:101755289
|
A | T | 11 | a0001c0001t0001g0108a0001c0001t0007g0012a0001c0001t0007g0105others(8): Show | 12 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.729-141A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101755289 | ||||||
| chr3:101755352
|
A | G | 13 | a0001c0001t0001g0108a0001c0001t0004g0013a0001c0001t0004g0304others(10): Show | 15 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.729-78A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101755352 | ||||||
| chr3:101755616
|
A | G | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.893+22A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 7/10 | chr3 | 101755616 | ||||||
| chr3:101755752
|
C | T | 4 | a0001c0001t0006g0020a0001c0001t0006g0216a0001c0001t0006g0217others(1): Show | 5 | HG02055.hp2 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.893+158C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 7/10 | chr3 | 101755752 | ||||||
| chr3:101755855
|
G | A | 110 | a0001c0001t0001g0108a0001c0001t0002g0001a0001c0001t0002g0002others(107): Show | 130 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.893+261G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 7/10 | chr3 | 101755855 | ||||||
| chr3:101755895
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.893+301C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 7/10 | chr3 | 101755895 | ||||||
| chr3:101755920
|
A | G | 1 | a0001c0001t0002g0170 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.893+326A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 7/10 | chr3 | 101755920 | ||||||
| chr3:101755985
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.893+391G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 7/10 | chr3 | 101755985 | ||||||
| chr3:101756017
|
G | C | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.893+423G>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 7/10 | chr3 | 101756017 | ||||||
| chr3:101756034
|
CG | C | 6 | a0001c0001t0001g0108a0001c0001t0010g0111a0001c0001t0010g0112others(3): Show | 6 | HG01884.hp2 HG02486.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.893+443delG | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr3 | 101756034 | |||||
| chr3:101756089
|
A | G | 110 | a0001c0001t0001g0108a0001c0001t0002g0001a0001c0001t0002g0002others(107): Show | 130 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.893+495A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 7/10 | chr3 | 101756089 | ||||||
| chr3:101756109
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.893+515G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 7/10 | chr3 | 101756109 | ||||||
| chr3:101756124
|
G | T | 3 | a0001c0001t0002g0017a0001c0001t0002g0150a0001c0001t0002g0153 | 4 | HG02080.hp1 NA19055.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.893+530G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 7/10 | chr3 | 101756124 | ||||||
| chr3:101756208
|
C | T | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.893+614C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 7/10 | chr3 | 101756208 | ||||||
| chr3:101756209
|
G | A | 13 | a0001c0001t0001g0108a0001c0001t0004g0013a0001c0001t0004g0304others(10): Show | 15 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.893+615G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 7/10 | chr3 | 101756209 | ||||||
| chr3:101756583
|
G | A | 72 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0027others(69): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.894-480G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 7/10 | chr3 | 101756583 | ||||||
| chr3:101756645
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.894-418T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 7/10 | chr3 | 101756645 | ||||||
| chr3:101756667
|
C | T | 2 | a0001c0002t0003g0127a0001c0013t0020g0307 | 2 | HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.894-396C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 7/10 | chr3 | 101756667 | ||||||
| chr3:101756760
|
A | G | 13 | a0001c0001t0001g0108a0001c0001t0004g0013a0001c0001t0004g0304others(10): Show | 15 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.894-303A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 7/10 | chr3 | 101756760 | ||||||
| chr3:101758611
|
C | G | 1 | a0001c0001t0001g0254 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1817+188C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101758611 | ||||||
| chr3:101758659
|
T | C | 1 | a0001c0001t0002g0158 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1817+236T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101758659 | ||||||
| chr3:101758713
|
G | A | 1 | a0009c0011t0001g0142 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1817+290G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101758713 | ||||||
| chr3:101758758
|
T | A | 3 | a0001c0001t0002g0001a0001c0001t0002g0188a0001c0001t0002g0189 | 7 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1817+335T>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101758758 | ||||||
| chr3:101758819
|
A | G | 1 | a0001c0002t0003g0127 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1817+396A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101758819 | ||||||
| chr3:101759201
|
C | T | 1 | a0001c0013t0020g0307 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1817+778C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101759201 | ||||||
| chr3:101759270
|
G | A | 1 | a0001c0001t0002g0160 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1817+847G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101759270 | ||||||
| chr3:101759412
|
T | A | 1 | a0001c0002t0009g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1817+989T>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101759412 | ||||||
| chr3:101759589
|
A | G | 4 | a0001c0001t0002g0005a0001c0001t0002g0147a0001c0001t0002g0148others(1): Show | 6 | NA18939.hp1 NA18941.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1817+1166A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101759589 | ||||||
| chr3:101759635
|
G | A | 1 | a0001c0013t0020g0307 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1817+1212G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101759635 | ||||||
| chr3:101759661
|
T | C | 13 | a0001c0001t0001g0108a0001c0001t0004g0013a0001c0001t0004g0304others(10): Show | 15 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1817+1238T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101759661 | ||||||
| chr3:101759687
|
T | G | 91 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(88): Show | 108 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.1817+1264T>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101759687 | ||||||
| chr3:101760022
|
C | CAA | 11 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0123others(8): Show | 12 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1817+1622_1817+162 others(6): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr3 | 101760022 | |||||
| chr3:101760022
|
C | CAAA | 16 | a0001c0001t0001g0121a0001c0001t0001g0225a0001c0001t0001g0229others(13): Show | 16 | HG01070.hp1 HG01884.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.1817+1621_1817+162 others(7): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr3 | 101760022 | |||||
| chr3:101760022
|
C | CAAAA | 45 | a0001c0001t0001g0227a0001c0001t0001g0290a0001c0001t0002g0001others(42): Show | 57 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1817+1620_1817+162 others(8): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr3 | 101760022 | |||||
| chr3:101760022
|
C | CAAAAA | 89 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(86): Show | 95 | HG00423.hp2 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.1817+1619_1817+162 others(9): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr3 | 101760022 | |||||
| chr3:101760022
|
C | CAAAAAA | 41 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0096others(38): Show | 42 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1817+1618_1817+162 others(10): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr3 | 101760022 | |||||
| chr3:101760022
|
CA | C | 6 | a0001c0002t0003g0127a0001c0002t0003g0130a0001c0002t0008g0116others(3): Show | 6 | HG01433.hp2 HG02698.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1817+1623delA | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr3 | 101760022 | |||||
| chr3:101760022
|
CAA | C | 17 | a0001c0002t0003g0004a0001c0002t0003g0014a0001c0002t0003g0015others(14): Show | 21 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.1817+1622_1817+162 others(6): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr3 | 101760022 | |||||
| chr3:101760022
|
CAAAAA | C | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0027others(75): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.1817+1619_1817+162 others(9): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr3 | 101760022 | |||||
| chr3:101760022
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0002g0316 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1817+1614_1817+162 others(14): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr3 | 101760022 | |||||
| chr3:101760047
|
G | A | 3 | a0001c0001t0001g0227a0001c0001t0001g0229a0001c0001t0001g0230 | 3 | NA18946.hp1 NA18947.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1817+1624G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101760047 | ||||||
| chr3:101760413
|
G | T | 312 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(309): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.1817+1990G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101760413 | ||||||
| chr3:101760553
|
G | A | 312 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(309): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.1818-1932G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101760553 | ||||||
| chr3:101760718
|
A | T | 1 | a0001c0001t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1818-1767A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101760718 | ||||||
| chr3:101760726
|
A | T | 1 | a0001c0001t0001g0085 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1818-1759A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101760726 | ||||||
| chr3:101760870
|
AT | A | 101 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0022others(98): Show | 103 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.1818-1606delT | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr3 | 101760870 | |||||
| chr3:101760898
|
T | C | 1 | a0001c0001t0027g0204 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1818-1587T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101760898 | ||||||
| chr3:101760988
|
G | A | 1 | a0001c0001t0006g0194 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1818-1497G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101760988 | ||||||
| chr3:101761097
|
C | A | 6 | a0001c0002t0008g0116a0001c0002t0008g0117a0001c0002t0008g0119others(3): Show | 6 | HG01433.hp2 HG02698.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.1818-1388C>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101761097 | ||||||
| chr3:101761100
|
C | T | 6 | a0001c0002t0008g0116a0001c0002t0008g0117a0001c0002t0008g0119others(3): Show | 6 | HG01433.hp2 HG02698.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.1818-1385C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101761100 | ||||||
| chr3:101761208
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1818-1277G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101761208 | ||||||
| chr3:101761312
|
C | T | 91 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(88): Show | 108 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.1818-1173C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101761312 | ||||||
| chr3:101761321
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0058 | 3 | HG02886.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1818-1164A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101761321 | ||||||
| chr3:101761382
|
G | A | 4 | a0001c0001t0002g0005a0001c0001t0002g0147a0001c0001t0002g0148others(1): Show | 6 | NA18939.hp1 NA18941.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1818-1103G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101761382 | ||||||
| chr3:101761478
|
T | C | 3 | a0001c0001t0006g0216a0001c0001t0006g0217a0001c0001t0006g0218 | 3 | HG02055.hp2 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1818-1007T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101761478 | ||||||
| chr3:101761815
|
G | A | 11 | a0001c0001t0001g0108a0001c0001t0007g0012a0001c0001t0007g0105others(8): Show | 12 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1818-670G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101761815 | ||||||
| chr3:101761911
|
C | G | 13 | a0001c0001t0001g0108a0001c0001t0004g0013a0001c0001t0004g0304others(10): Show | 15 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1818-574C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101761911 | ||||||
| chr3:101762135
|
T | A | 1 | a0001c0001t0031g0122 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1818-350T>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101762135 | ||||||
| chr3:101762240
|
G | A | 1 | a0001c0001t0026g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1818-245G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101762240 | ||||||
| chr3:101762752
|
A | T | 1 | a0001c0002t0003g0127 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1893+192A>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | chr3 | 101762752 | ||||||
| chr3:101762797
|
G | A | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1893+237G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | chr3 | 101762797 | ||||||
| chr3:101763137
|
C | T | 1 | a0001c0013t0020g0307 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1893+577C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | chr3 | 101763137 | ||||||
| chr3:101763323
|
A | G | 2 | a0001c0001t0011g0143a0009c0011t0001g0142 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1893+763A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | chr3 | 101763323 | ||||||
| chr3:101763466
|
C | T | 3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0101 | 3 | HG02698.hp2 HG02735.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1893+906C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | chr3 | 101763466 | ||||||
| chr3:101763570
|
C | T | 1 | a0001c0001t0004g0084 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1893+1010C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | chr3 | 101763570 | ||||||
| chr3:101763590
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1893+1030C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | chr3 | 101763590 | ||||||
| chr3:101763688
|
G | C | 1 | a0001c0001t0004g0076 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1893+1128G>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | chr3 | 101763688 | ||||||
| chr3:101763739
|
A | G | 1 | a0001c0001t0002g0177 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1894-1108A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | chr3 | 101763739 | ||||||
| chr3:101763782
|
C | T | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1894-1065C>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | chr3 | 101763782 | ||||||
| chr3:101763875
|
ACATTATT others(33): Show |
A | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(93): Show | 114 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1894-955_1894-916d others(42): Show |
CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 101763875 | |||||
| chr3:101763935
|
A | C | 1 | a0001c0001t0002g0310 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1894-912A>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | chr3 | 101763935 | ||||||
| chr3:101764229
|
G | A | 13 | a0001c0001t0001g0108a0001c0001t0004g0013a0001c0001t0004g0304others(10): Show | 15 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1894-618G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | chr3 | 101764229 | ||||||
| chr3:101764364
|
C | A | 71 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0027others(68): Show | 74 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1894-483C>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | chr3 | 101764364 | ||||||
| chr3:101764465
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1894-382G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | chr3 | 101764465 | ||||||
| chr3:101764474
|
G | A | 7 | a0001c0001t0002g0154a0001c0001t0002g0163a0001c0001t0002g0166others(4): Show | 7 | HG02258.hp2 HG02572.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1894-373G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | chr3 | 101764474 | ||||||
| chr3:101764560
|
G | A | 1 | a0001c0002t0003g0136 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1894-287G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | chr3 | 101764560 | ||||||
| chr3:101764611
|
C | CA | 19 | a0001c0001t0001g0024a0001c0001t0001g0269a0001c0001t0001g0285others(16): Show | 19 | HG00735.hp1 HG01169.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.1894-219dupA | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 101764611 | |||||
| chr3:101764611
|
CA | C | 6 | a0001c0001t0001g0058a0001c0001t0001g0234a0001c0001t0002g0147others(3): Show | 6 | HG01070.hp2 HG01099.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1894-219delA | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 101764611 | |||||
| chr3:101764816
|
T | C | 1 | a0001c0001t0017g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1894-31T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | chr3 | 101764816 |