Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | MAVAR others(860): Show |
chr3 | 101719614 | 101775562 |
| a0002 | 0/0 | 865 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | MAVAR others(860): Show |
chr3 | 101719614 | 101775562 |
| a0003 | 0/0 | 865 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | MAVAR others(860): Show |
chr3 | 101719614 | 101775562 |
| a0004 | 0/0 | 865 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CEP97_chr3_101719614_101775562 | CEP97 | MAVAR others(860): Show |
chr3 | 101719614 | 101775562 |
| a0005 | 0/0 | 865 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | MAVAR others(860): Show |
chr3 | 101719614 | 101775562 |
| a0006 | 0/0 | 865 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | MAVAR others(860): Show |
chr3 | 101719614 | 101775562 |
| a0007 | 0/0 | 865 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | MAVAR others(860): Show |
chr3 | 101719614 | 101775562 |
| a0008 | 0/0 | 607 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | MAVAR others(602): Show |
chr3 | 101719614 | 101775562 |
| a0009 | 0/0 | 865 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | MAVAR others(860): Show |
chr3 | 101719614 | 101775562 |
| a0010 | 0/0 | 865 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | MAVAR others(860): Show |
chr3 | 101719614 | 101775562 |
| a0011 | 0/0 | 865 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | MAVAR others(860): Show |
chr3 | 101719614 | 101775562 |
| a0012 | 0/0 | 865 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | MAVAR others(860): Show |
chr3 | 101719614 | 101775562 |
| a0013 | 0/0 | 865 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | MAVAR others(860): Show |
chr3 | 101719614 | 101775562 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2595 | 298 | 69 | 47 | 149 | 6 | 26 | CEP97_chr3_101719614_101775562 | CEP97 | ATGGC others(2590): Show |
chr3 | 101719614 | 101775562 | ||
| a0001c0002 | 1/0 | 2595 | 34 | 13 | 10 | 2 | 4 | 4 | CEP97_chr3_101719614_101775562 | CEP97 | ATGGC others(2590): Show |
chr3 | 101719614 | 101775562 | ||
| a0001c0008 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | ATGGC others(2590): Show |
chr3 | 101719614 | 101775562 | ||
| a0001c0013 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | ATGGC others(2590): Show |
chr3 | 101719614 | 101775562 | ||
| a0001c0015 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | ATGGC others(2590): Show |
chr3 | 101719614 | 101775562 | ||
| a0001c0016 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | ATGGC others(2590): Show |
chr3 | 101719614 | 101775562 | ||
| a0002c0003 | 0/0 | 2595 | 3 | 2 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | ATGGC others(2590): Show |
chr3 | 101719614 | 101775562 | ||
| a0003c0005 | 0/0 | 2595 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | ATGGC others(2590): Show |
chr3 | 101719614 | 101775562 | ||
| a0004c0004 | 0/0 | 2595 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | ATGGC others(2590): Show |
chr3 | 101719614 | 101775562 | ||
| a0005c0009 | 0/0 | 2595 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | ATGGC others(2590): Show |
chr3 | 101719614 | 101775562 | ||
| a0006c0017 | 0/0 | 2595 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | ATGGC others(2590): Show |
chr3 | 101719614 | 101775562 | ||
| a0007c0006 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | ATGGC others(2590): Show |
chr3 | 101719614 | 101775562 | ||
| a0008c0014 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | ATGGC others(2590): Show |
chr3 | 101719614 | 101775562 | ||
| a0009c0018 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | ATGGC others(2590): Show |
chr3 | 101719614 | 101775562 | ||
| a0010c0011 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | ATGGC others(2590): Show |
chr3 | 101719614 | 101775562 | ||
| a0011c0007 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | ATGGC others(2590): Show |
chr3 | 101719614 | 101775562 | ||
| a0012c0010 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | ATGGC others(2590): Show |
chr3 | 101719614 | 101775562 | ||
| a0013c0012 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | ATGGC others(2590): Show |
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 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0002 | 0/0 | 7672 | 96 | 18 | 17 | 52 | 2 | 7 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0004 | 0/0 | 7674 | 19 | 4 | 3 | 7 | 2 | 3 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7669): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0005 | 0/0 | 7672 | 12 | 1 | 0 | 11 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0006 | 0/0 | 7674 | 7 | 5 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7669): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0007 | 0/0 | 7676 | 6 | 6 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7671): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0010 | 0/0 | 7676 | 3 | 3 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7671): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0011 | 0/0 | 7673 | 3 | 1 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7668): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0012 | 0/0 | 7672 | 3 | 0 | 0 | 3 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0013 | 0/0 | 7676 | 2 | 2 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7671): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0014 | 0/0 | 7675 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7670): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0015 | 0/0 | 7672 | 2 | 2 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0016 | 0/0 | 7672 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0017 | 0/0 | 7674 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7669): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0019 | 0/1 | 7672 | 1 | 0 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0021 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0022 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0023 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0024 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0025 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0026 | 0/0 | 7672 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0027 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0030 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0031 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0001t0032 | 0/0 | 7672 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0002t0003 | 0/0 | 7672 | 22 | 8 | 9 | 0 | 4 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0002t0008 | 0/0 | 7672 | 5 | 0 | 1 | 2 | 0 | 2 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0002t0009 | 1/0 | 7672 | 5 | 4 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGATT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0002t0018 | 0/0 | 7674 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7669): Show |
chr3 | 101719614 | 101775562 |
| a0001c0002t0028 | 0/0 | 7673 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7668): Show |
chr3 | 101719614 | 101775562 |
| a0001c0008t0004 | 0/0 | 7674 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7669): Show |
chr3 | 101719614 | 101775562 |
| a0001c0013t0020 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0015t0001 | 0/0 | 7672 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0001c0016t0029 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0002c0003t0002 | 0/0 | 7672 | 3 | 2 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0003c0005t0001 | 0/0 | 7672 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0004c0004t0002 | 0/0 | 7672 | 2 | 0 | 0 | 2 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0005c0009t0001 | 0/0 | 7672 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0006c0017t0002 | 0/0 | 7672 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0007c0006t0002 | 0/0 | 7672 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0008c0014t0001 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0009c0018t0001 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0010c0011t0001 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0011c0007t0001 | 0/0 | 7672 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0012c0010t0001 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
chr3 | 101719614 | 101775562 |
| a0013c0012t0001 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | AGACT others(7667): Show |
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 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0235 | 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 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| 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 |
| a0001c0001t0001g0260 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0001g0312 | 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 |
| a0001c0001t0002g0003 | 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 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0309 | 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 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 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 |
| 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 |
| a0001c0001t0004g0303 | 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 |
| a0001c0001t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| 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 |
| a0001c0001t0010g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0011g0142 | 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 |
| a0001c0001t0011g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0012g0299 | 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 |
| 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 |
| a0001c0001t0015g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0015g0278 | 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 |
| a0001c0001t0017g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0001t0019g0250 | 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 |
| a0001c0001t0025g0281 | 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 |
| a0001c0001t0027g0203 | 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 |
| a0001c0002t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0003g0138 | 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 |
| a0001c0002t0003g0302 | 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 |
| a0001c0002t0009g0002 | 1/0 | 4 | 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 |
| a0001c0002t0018g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0001c0002t0028g0137 | 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 |
| a0001c0013t0020g0306 | 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 |
| a0002c0003t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0002c0003t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0002c0003t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0003c0005t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0003c0005t0001g0283 | 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 |
| a0005c0009t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0006c0017t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0007c0006t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0008c0014t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0009c0018t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0010c0011t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0011c0007t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0012c0010t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| a0013c0012t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 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 | g0186 | 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 | g0128 | 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 | g0246 | 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 | g0207 | EAS | CHS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0182 | 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 | g0244 | 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 | g0248 | EAS | CHS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00609 | hp2 | a0001 | c0001 | t0006 | g0193 | EAS | CHS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | CHS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00621 | hp2 | a0003 | c0005 | t0001 | g0283 | EAS | CHS | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0240 | 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 | g0236 | 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 | g0289 | 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 | g0293 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG00735 | hp2 | a0005 | 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 | g0161 | 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 | g0287 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01069 | hp1 | a0006 | c0017 | t0002 | g0199 | 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 | g0188 | 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 | g0127 | 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 | g0302 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01106 | hp1 | a0001 | c0002 | t0003 | g0135 | 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 | g0290 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0201 | 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 | g0131 | 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 | g0208 | AMR | PUR | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0212 | 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 | g0262 | AMR | CLM | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0202 | 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 | g0190 | 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 | g0268 | 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 | g0261 | 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 | a0007 | 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 | g0292 | 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 | g0213 | 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 | g0263 | 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 | g0159 | AMR | PEL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | PEL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0151 | 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 | g0145 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02027 | hp1 | a0008 | c0014 | t0001 | g0051 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0216 | 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 | g0266 | 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 | g0277 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0149 | 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 | g0307 | 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 | g0200 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0291 | 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 | g0227 | 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 | g0280 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0260 | 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 | g0303 | 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 | g0233 | EAS | KHV | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02572 | hp1 | a0009 | c0018 | t0001 | g0234 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0171 | 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 | g0274 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02622 | hp2 | a0001 | c0002 | t0009 | g0002 | 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 | g0206 | 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 | g0311 | 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 | g0189 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0284 | 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 | g0136 | 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 | g0211 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0279 | 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 | g0170 | 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 | g0129 | 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 | g0166 | AFR | ESN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0308 | 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 | g0137 | AFR | MSL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ESN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03130 | hp2 | a0001 | c0001 | t0015 | g0241 | 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 | g0315 | 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 | g0134 | 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 | g0286 | 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 | a0010 | c0011 | t0001 | g0141 | 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 | g0215 | AFR | MSL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03486 | hp2 | a0001 | c0002 | t0003 | g0138 | AFR | MSL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0160 | 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 | g0184 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ESN | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03516 | hp2 | a0001 | c0002 | t0003 | g0126 | 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 | g0288 | 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 | g0217 | 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 | g0175 | 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 | g0295 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03710 | hp1 | a0001 | c0002 | t0003 | g0132 | SAS | PJL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0285 | 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 | g0218 | 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 | g0204 | SAS | STU | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG04115 | hp2 | a0011 | 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 | g0156 | EAS | CHB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0237 | 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 | g0140 | AFR | YRI | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0163 | 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 | g0221 | 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 | g0192 | 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 | g0228 | 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 | g0178 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0164 | 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 | g0230 | 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 | g0003 | 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 | g0179 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0195 | 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 | g0222 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18961 | hp2 | a0001 | c0001 | t0012 | g0300 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0196 | 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 | g0147 | 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 | g0309 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0242 | 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 | g0003 | 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 | g0276 | 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 | g0177 | 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 | g0297 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18979 | hp2 | a0001 | c0001 | t0011 | g0270 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0003 | 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 | g0183 | 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 | g0238 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18988 | hp1 | a0001 | c0001 | t0027 | g0203 | 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 | g0231 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0150 | 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 | g0174 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0191 | 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 | g0239 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19011 | hp1 | a0001 | c0001 | t0012 | g0299 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19030 | hp1 | a0001 | c0013 | t0020 | g0306 | 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 | g0002 | AFR | LWK | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0272 | 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 | g0197 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0152 | 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 | g0245 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0173 | 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 | a0012 | c0010 | t0001 | g0247 | 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 | g0154 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0003 | 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 | g0220 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0146 | 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 | g0223 | 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 | a0013 | c0012 | t0001 | g0232 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0172 | 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 | g0155 | 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 | g0301 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0226 | 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 | g0265 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | YRI | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA19240 | hp2 | a0001 | c0001 | t0011 | g0142 | AFR | YRI | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | ASW | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0314 | 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 | g0133 | 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 | g0294 | 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 | g0130 | 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 | g0002 | AFR | ACB | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03471 | hp1 | a0001 | c0002 | t0003 | g0139 | AFR | MSL | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| HG03471 | hp2 | a0001 | c0001 | t0015 | g0278 | 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 | g0185 | AFR | USA | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | USA | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| NA20300 | hp2 | a0001 | c0001 | t0025 | g0281 | 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 | g0143 | AFR | LWK | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0019 | g0250 | REF | REF | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0009 | g0002 | REF | REF | CEP97_chr3_101719614_101775562 | CEP97 | chr3 | 101719614 | 101775562 |
| view | 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 | a0007 | 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 | a0009 | 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 | a0006 | 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 | a0011 | 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 | a0006 | 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 | a0005 | 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 | a0012 | 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 | a0010 | 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 | a0008 | 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 | a0013 | 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 |
| view | 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 | a0001c0001 a0001c0008 a0001c0013 others(13): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(313): 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 |
| view | 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 | 44 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(41): Show |
346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): 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 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0014 others(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 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0013 |
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 | ||||||
| chr3:101766924 | 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 | a0001c0002t0003 a0001c0002t0028 a0001c0016t0029 |
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 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 others(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 | 41 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(38): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): 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 | a0001c0001t0005 a0001c0001t0022 a0001c0001t0030 |
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 | a0001c0001t0011 a0001c0001t0014 a0001c0002t0028 |
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 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 others(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 |
| view | 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 | a0001c0001t0002g0025 a0001c0001t0002g0313 a0001c0001t0002g0314 others(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 | a0001c0001t0001g0312 | 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 | a0001c0001t0001g0311 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | a0001c0001t0002g0310 | 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 | a0001c0001t0002g0309 | 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 | a0001c0001t0010g0308 | 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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0028 others(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 | a0001c0001t0001g0312 | 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 | a0001c0002t0003g0302 | 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 | a0001c0001t0012g0299 a0001c0001t0012g0300 a0001c0001t0012g0301 |
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 | 100 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(97): Show |
102 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(99): 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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0017g0143 | 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 | a0001c0001t0010g0308 | 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 | a0001c0001t0002g0016 a0001c0001t0002g0144 a0001c0001t0002g0145 |
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 | a0001c0001t0006g0020 a0001c0001t0006g0215 a0001c0001t0006g0216 others(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 | a0001c0001t0001g0218 | 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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(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 | a0001c0001t0002g0214 a0001c0001t0006g0020 a0001c0001t0006g0215 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0079 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0146 a0001c0001t0002g0147 others(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 | a0001c0001t0011g0142 a0010c0011t0001g0141 |
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 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(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 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0003 others(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 | a0001c0001t0017g0143 | 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 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0222 a0001c0001t0001g0223 others(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 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0149 a0001c0001t0002g0150 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0312 a0001c0001t0004g0013 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 |
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 | a0001c0001t0017g0143 | 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 | a0001c0001t0002g0006 a0001c0001t0002g0155 a0001c0001t0002g0156 others(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 | a0001c0001t0002g0149 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0115 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0282 a0001c0001t0001g0284 others(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 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0094 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0233 a0001c0001t0002g0025 a0001c0001t0002g0206 others(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 | a0001c0001t0001g0231 a0001c0001t0002g0001 a0001c0001t0002g0003 others(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 | a0001c0001t0001g0108 a0001c0001t0002g0309 a0001c0001t0004g0013 others(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 | a0001c0001t0007g0012 a0001c0001t0007g0105 a0001c0001t0007g0106 others(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 | a0001c0001t0001g0102 a0001c0001t0001g0279 a0001c0001t0001g0280 others(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 | a0001c0001t0001g0312 a0001c0001t0002g0154 a0001c0001t0002g0158 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | a0001c0001t0005g0011 a0001c0001t0005g0056 a0001c0001t0005g0061 others(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 | a0001c0001t0017g0143 | 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 | 291 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(288): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(313): 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 | a0001c0001t0001g0094 a0001c0001t0001g0115 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0297 a0001c0001t0001g0312 a0001c0001t0002g0201 others(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 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
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 | a0001c0001t0001g0108 a0001c0001t0001g0297 a0001c0001t0007g0012 others(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 | 140 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(137): Show |
158 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(155): 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 | a0001c0001t0001g0244 a0001c0001t0002g0146 a0001c0001t0002g0155 others(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 | a0001c0002t0003g0135 | 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 | a0001c0001t0001g0297 | 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 | a0001c0001t0001g0297 | 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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0002g0150 | 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 | a0001c0001t0015g0278 | 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 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0001g0108 a0001c0001t0004g0013 a0001c0001t0004g0303 others(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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0115 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0053 a0001c0001t0021g0052 a0008c0014t0001g0051 |
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 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(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 | a0001c0001t0001g0297 | 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 | 99 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(96): Show |
101 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(98): 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 | a0001c0001t0017g0143 | 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 | a0001c0001t0007g0012 a0001c0001t0007g0105 a0001c0001t0007g0106 others(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 | a0001c0001t0007g0012 a0001c0001t0007g0105 a0001c0001t0007g0106 others(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 | a0001c0001t0007g0012 a0001c0001t0007g0105 a0001c0001t0007g0106 others(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 | a0001c0001t0007g0012 a0001c0001t0007g0105 a0001c0001t0007g0106 others(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 | a0001c0001t0017g0143 | 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 | a0001c0001t0001g0108 a0001c0001t0004g0013 a0001c0001t0004g0303 others(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 | a0001c0001t0004g0073 a0001c0001t0004g0088 a0001c0001t0004g0089 others(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 | a0001c0001t0017g0143 | 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 | a0001c0013t0020g0306 | 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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0001g0297 | 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 | a0001c0001t0002g0197 | 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 | a0001c0001t0002g0206 | 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 | a0001c0001t0002g0162 | 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 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0094 a0001c0001t0001g0115 a0001c0001t0001g0121 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0127 others(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 | a0001c0001t0017g0143 | 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 | a0001c0002t0003g0134 a0001c0002t0003g0136 a0001c0002t0028g0137 |
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 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(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 | a0001c0001t0017g0143 | 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 | 291 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(288): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(313): 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 | a0001c0001t0001g0108 a0001c0001t0007g0012 a0001c0001t0007g0105 others(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 | 291 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(288): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(313): 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 | a0001c0001t0001g0297 | 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0004c0004t0002g0018 |
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 | a0001c0001t0001g0242 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0003 others(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 | a0001c0001t0011g0142 a0010c0011t0001g0141 |
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 | a0001c0001t0001g0108 a0001c0001t0004g0013 a0001c0001t0004g0303 others(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 | a0001c0001t0002g0196 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0146 a0001c0001t0002g0147 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0017g0143 | 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 | a0001c0001t0006g0020 a0001c0001t0006g0215 a0001c0001t0006g0216 others(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 | 116 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(113): Show |
123 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(120): 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 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0001t0001g0123 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0001c0001t0006g0020 a0001c0001t0006g0215 a0001c0001t0006g0216 others(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 | a0001c0001t0002g0214 | 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 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0001g0229 |
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 | 291 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(288): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(313): 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 | a0001c0001t0001g0094 a0001c0001t0001g0115 a0001c0001t0001g0121 others(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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0145 | 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 | a0001c0002t0003g0129 | 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 | a0001c0002t0008g0116 a0001c0002t0008g0117 a0001c0002t0008g0119 others(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 | a0001c0001t0001g0293 | 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 | a0001c0001t0001g0108 a0001c0001t0001g0312 a0001c0001t0004g0013 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | ||||||
| chr3:101740099 | 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 | a0001c0001t0001g0108 a0001c0001t0004g0013 a0001c0001t0004g0303 others(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 | a0001c0001t0001g0311 | 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 | a0001c0001t0001g0108 a0001c0001t0004g0013 a0001c0001t0004g0303 others(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 | a0001c0001t0011g0142 a0010c0011t0001g0141 |
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 | a0001c0001t0002g0172 a0001c0001t0002g0191 a0001c0001t0002g0192 others(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 | a0001c0001t0001g0108 a0001c0001t0004g0013 a0001c0001t0004g0303 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0231 a0001c0001t0001g0235 others(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 | a0001c0002t0003g0126 | 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 | a0001c0001t0027g0203 | 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 | a0001c0001t0001g0249 a0001c0001t0001g0264 a0001c0001t0001g0265 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | 100 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(97): Show |
103 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(100): 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 | a0001c0001t0017g0143 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0115 |
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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0013t0020g0306 | 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 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 |
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 | a0001c0001t0001g0079 a0001c0001t0001g0096 a0001c0001t0001g0245 others(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 | a0001c0001t0002g0157 a0001c0001t0002g0165 a0001c0001t0002g0166 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0002g0179 | 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 | a0001c0001t0017g0143 | 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 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0003 others(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 | 317 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(314): Show |
346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): 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 | a0001c0001t0001g0115 a0001c0001t0001g0227 a0001c0001t0001g0246 others(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 | a0001c0001t0001g0049 a0001c0002t0003g0128 |
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 | 317 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(314): Show |
346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): 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 | a0001c0013t0020g0306 | 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 | 102 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(99): Show |
105 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(102): 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 | a0001c0001t0017g0143 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0254 a0001c0001t0001g0255 others(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 | a0001c0001t0001g0108 a0001c0001t0004g0013 a0001c0001t0004g0303 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0115 a0001c0001t0001g0121 others(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 | a0001c0001t0002g0212 | 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 | a0001c0001t0001g0108 a0001c0001t0004g0013 a0001c0001t0004g0303 others(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 | 292 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(289): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(315): 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 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0108 a0001c0001t0004g0073 a0001c0001t0007g0012 others(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 | a0001c0001t0017g0143 | 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 | a0001c0001t0017g0143 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0011g0142 a0010c0011t0001g0141 |
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 | a0001c0001t0002g0309 a0001c0001t0012g0299 a0001c0001t0012g0300 others(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 | a0001c0002t0003g0126 | 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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0001g0263 | 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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0100 a0001c0001t0004g0086 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0187 a0001c0001t0002g0188 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0011g0142 a0010c0011t0001g0141 |
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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0001g0108 a0001c0001t0004g0013 a0001c0001t0004g0303 others(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 | a0001c0001t0015g0241 a0001c0001t0015g0278 |
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 | a0001c0001t0017g0143 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0115 a0001c0001t0001g0121 others(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 | a0001c0001t0002g0025 a0001c0001t0002g0313 a0001c0001t0002g0314 others(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 | a0001c0001t0001g0274 | 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 | a0001c0001t0002g0169 a0001c0001t0002g0170 |
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 | a0001c0001t0001g0108 a0001c0001t0013g0109 a0001c0001t0013g0110 |
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 | a0001c0001t0004g0013 a0001c0001t0004g0303 |
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 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0059 others(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 | a0001c0001t0002g0173 a0001c0001t0002g0198 |
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 | a0001c0001t0017g0143 | 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 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
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 | a0001c0001t0002g0173 a0001c0001t0002g0198 |
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 | a0001c0001t0001g0238 | 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 | a0001c0001t0001g0238 | 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 | a0001c0001t0001g0264 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0047 |
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 | a0001c0001t0011g0142 a0010c0011t0001g0141 |
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 | a0001c0001t0001g0108 a0001c0001t0004g0013 a0001c0001t0004g0303 others(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 | a0001c0001t0001g0240 | 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 | a0001c0001t0006g0217 | 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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0017g0143 | 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 | a0001c0001t0001g0099 a0001c0001t0001g0255 |
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 | a0001c0001t0017g0143 | 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 | a0001c0001t0017g0143 | 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 | 311 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(308): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): 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 | a0001c0001t0015g0241 a0001c0001t0015g0278 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0003 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0046 a0001c0001t0001g0223 others(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 | a0001c0001t0001g0049 a0001c0001t0001g0074 a0001c0001t0002g0001 others(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 | a0001c0002t0003g0126 | 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 | a0001c0001t0001g0238 a0001c0001t0001g0272 a0001c0002t0003g0004 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | 7 | a0001c0001t0001g0023 a0001c0001t0001g0260 a0001c0001t0001g0261 others(4): Show |
7 | HG00642.hp1 HG01346.hp1 HG01358.hp1 others(4): 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 | a0001c0001t0001g0041 a0001c0001t0001g0049 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0028 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0094 a0001c0001t0001g0115 others(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 | 88 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(85): Show |
92 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(89): 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 | a0001c0001t0001g0079 a0001c0001t0001g0223 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0239 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | 311 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(308): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.729-6974C>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101748456 | |||||||
| chr3:101748701 | C | T | 101 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(98): Show |
103 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(100): 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 | a0001c0001t0001g0291 | 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 | a0001c0001t0011g0142 a0010c0011t0001g0141 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0218 others(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 | |||||||
| chr3:101748939 | C | T | 3 | a0001c0001t0001g0244 a0001c0001t0001g0282 a0013c0012t0001g0232 |
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 | a0001c0001t0002g0214 a0001c0001t0006g0020 a0001c0001t0006g0215 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0058 |
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 | a0001c0001t0001g0240 a0001c0001t0015g0241 a0001c0001t0015g0278 others(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 | a0001c0001t0017g0143 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0261 a0001c0001t0001g0284 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0115 a0001c0001t0001g0121 others(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 | a0001c0002t0003g0126 | 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 | a0001c0001t0002g0145 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | a0001c0001t0010g0111 a0001c0001t0010g0112 a0001c0001t0010g0308 |
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 | 280 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(277): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.729-5820A>G | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101749610 | |||||||
| chr3:101749749 | T | C | 100 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(97): Show |
103 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(100): 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 | a0001c0001t0001g0094 a0001c0001t0001g0115 a0001c0001t0001g0121 others(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 | a0001c0001t0002g0214 | 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 | a0001c0001t0002g0214 | 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 | a0001c0001t0006g0020 a0001c0001t0006g0215 a0001c0001t0006g0216 others(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 | a0001c0001t0002g0214 | 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 | a0001c0001t0002g0214 | 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 | a0001c0001t0002g0214 | 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 | a0001c0001t0002g0214 | 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 | a0001c0001t0002g0214 | 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 | a0001c0001t0002g0214 a0001c0001t0023g0103 a0001c0001t0026g0114 |
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 | a0001c0001t0002g0214 | 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 | a0001c0001t0002g0214 | 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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0004g0303 | 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 | a0001c0001t0017g0143 | 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 | a0001c0001t0002g0180 | 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 | a0001c0001t0001g0233 | 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 | 102 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(99): Show |
105 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(102): 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 | a0001c0013t0020g0306 | 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 | a0001c0001t0011g0142 a0010c0011t0001g0141 |
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 | a0001c0001t0001g0307 a0001c0001t0017g0143 |
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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0115 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0003 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0284 a0001c0001t0001g0285 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0108 a0001c0001t0001g0284 others(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 | a0001c0002t0003g0133 | 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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0013t0020g0306 | 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 | a0001c0001t0001g0224 | 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 | a0001c0002t0003g0004 a0001c0002t0003g0015 a0001c0002t0003g0127 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0237 a0001c0001t0001g0238 others(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 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 |
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 | a0001c0001t0001g0094 a0001c0001t0001g0115 a0001c0001t0001g0121 others(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 | a0003c0005t0001g0283 | 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 | a0001c0001t0001g0108 a0001c0001t0004g0013 a0001c0001t0004g0303 others(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 | 100 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(97): Show |
102 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(99): 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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | 292 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(289): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.729-1801T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101753629 | |||||||
| chr3:101753657 | G | C | 291 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(288): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(313): 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 | a0001c0001t0001g0108 a0001c0001t0004g0013 a0001c0001t0004g0303 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0001g0108 a0001c0001t0007g0012 a0001c0001t0007g0105 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0115 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0003 others(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 | 159 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(156): Show |
164 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(161): 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 | a0001c0001t0001g0043 a0001c0001t0001g0102 a0001c0001t0001g0108 others(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 | a0001c0001t0002g0019 a0001c0001t0002g0144 a0001c0001t0002g0148 others(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 | 310 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(307): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): 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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0002c0003t0002g0208 a0002c0003t0002g0211 a0002c0003t0002g0213 |
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 | a0001c0001t0002g0214 | 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 | a0001c0001t0002g0025 a0001c0001t0002g0313 a0001c0001t0002g0314 others(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 | 47 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(44): Show |
48 | HG00323.hp1 HG00558.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.729-634G>A | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 6/10 | chr3 | 101754796 | |||||||
| chr3:101754896 | A | AT | 107 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(104): Show |
110 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(107): 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 | a0001c0001t0001g0049 a0001c0001t0002g0187 a0001c0001t0002g0206 others(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 | a0011c0007t0001g0055 | 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 | a0001c0001t0001g0108 a0001c0001t0007g0012 a0001c0001t0007g0105 others(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 | a0001c0001t0001g0108 a0001c0001t0004g0013 a0001c0001t0004g0303 others(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 | a0001c0001t0017g0143 | 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 | a0001c0001t0006g0020 a0001c0001t0006g0215 a0001c0001t0006g0216 others(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 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0003 others(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 | a0001c0001t0002g0168 | 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 | a0001c0001t0002g0214 | 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 | a0001c0001t0001g0108 a0001c0001t0010g0111 a0001c0001t0010g0112 others(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 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0003 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0149 a0001c0001t0002g0152 |
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 | a0001c0001t0002g0214 | 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 | a0001c0001t0001g0108 a0001c0001t0004g0013 a0001c0001t0004g0303 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | a0001c0002t0003g0126 a0001c0013t0020g0306 |
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 | a0001c0001t0001g0108 a0001c0001t0004g0013 a0001c0001t0004g0303 others(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 | a0001c0001t0002g0156 | 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 | a0010c0011t0001g0141 | 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 | a0001c0001t0002g0001 a0001c0001t0002g0187 a0001c0001t0002g0188 |
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 | a0001c0002t0003g0126 | 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 | a0001c0013t0020g0306 | 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 | a0001c0001t0002g0159 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0146 a0001c0001t0002g0147 others(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 | a0001c0013t0020g0306 | 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 | a0001c0001t0001g0108 a0001c0001t0004g0013 a0001c0001t0004g0303 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0115 a0001c0001t0001g0123 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0224 a0001c0001t0001g0228 others(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 | a0001c0001t0001g0226 a0001c0001t0001g0289 a0001c0001t0002g0001 others(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 | 88 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(85): Show |
94 | HG00423.hp2 HG00639.hp2 HG00642.hp1 others(91): 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 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0096 others(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 | a0001c0002t0003g0126 a0001c0002t0003g0129 a0001c0002t0008g0116 others(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 | a0001c0002t0003g0004 a0001c0002t0003g0014 a0001c0002t0003g0015 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | a0001c0001t0002g0315 | 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 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0001g0229 |
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 | 311 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(308): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1817+1990G>T | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 9/10 | chr3 | 101760413 | |||||||
| chr3:101760553 | G | A | 311 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(308): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): 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 | 100 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(97): Show |
102 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(99): 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 | a0001c0001t0027g0203 | 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 | a0001c0001t0006g0193 | 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 | a0001c0002t0008g0116 a0001c0002t0008g0117 a0001c0002t0008g0119 others(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 | a0001c0002t0008g0116 a0001c0002t0008g0117 a0001c0002t0008g0119 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0058 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0146 a0001c0001t0002g0147 others(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 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 |
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 | a0001c0001t0001g0108 a0001c0001t0007g0012 a0001c0001t0007g0105 others(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 | a0001c0001t0001g0108 a0001c0001t0004g0013 a0001c0001t0004g0303 others(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 | a0001c0002t0003g0126 | 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 | a0001c0001t0002g0214 | 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 | a0001c0013t0020g0306 | 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 | a0001c0001t0011g0142 a0010c0011t0001g0141 |
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 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0101 |
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 | a0001c0001t0001g0218 | 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 | a0001c0001t0002g0175 | 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 | a0001c0001t0002g0214 | 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 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(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 | a0001c0001t0002g0309 | 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 | a0001c0001t0001g0108 a0001c0001t0004g0013 a0001c0001t0004g0303 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0260 | 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 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0167 others(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 | a0001c0002t0003g0135 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0268 a0001c0001t0001g0284 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0233 a0001c0001t0002g0146 others(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 | a0001c0001t0017g0143 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1894-31T>C | CEP97 | ENSG00000182504.12 | transcript | ENST00000341893.8 | protein_coding | 10/10 | chr3 | 101764816 |