Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:8176331-8176492 | Rare:50 | ||||
chr17:8248042-8248142 | Common:2; Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
chr17:10697510-10697649 | Common:3; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
chr17:14069447-14069539 | Common:1; Rare:29; Clinvar (benign):2 | ||||
chr17:15262505-15262645 | Rare:36 | ||||
chr17:17591595-17591926 | Common:1; Rare:94 | ||||
chr17:18087803-18087964 | Rare:39 | ||||
chr17:19378180-19378494 | Common:1; Rare:75 | ||||
chr17:21214151-21214351 | Common:2; Rare:92 | ||||
chr17:28335429-28335768 | Common:1; Rare:76 | ||||
chr17:28357467-28357647 | Common:5; Rare:86 | ||||
chr17:28598994-28599153 | Common:2; Rare:44 | ||||
chr17:28661896-28662256 | Common:1; Rare:124 | ||||
chr17:28718151-28718348 | Rare:54 | ||||
chr17:29294113-29294297 | Common:1; Rare:68 |