Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:15563430-15563749 | Common:1; Rare:106 | ||||
chr17:15699521-15699794 | Common:3; Rare:74 | ||||
chr17:15999435-15999486 | Rare:22 | ||||
chr17:15999505-16000227 | Common:4; Rare:300; Clinvar:8; Clinvar (benign):16; Clinvar (pathogenic):2 | ||||
chr17:16024716-16025028 | Common:3; Rare:55 | ||||
chr17:16215387-16215695 | Common:2; Rare:128 | ||||
chr17:16217094-16217306 | Rare:71; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr17:16353029-16353231 | Rare:66 | ||||
chr17:16353381-16353686 | Rare:96 | ||||
chr17:16380605-16380810 | Common:3; Rare:45 | ||||
chr17:16492163-16492243 | Common:1; Rare:24 | ||||
chr17:17237109-17237693 | Common:8; Rare:164; Clinvar:1; Clinvar (benign):3 | ||||
chr17:17303238-17303387 | Common:1; Rare:53 | ||||
chr17:17591400-17591487 | Rare:28 | ||||
chr17:17591534-17591923 | Common:2; Rare:114 |