Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:10729995-10730128 | Common:3; Rare:29 | ||||
chr17:11997444-11997573 | Rare:44 | ||||
chr17:13017996-13018278 | Common:5; Rare:78 | ||||
chr17:14069384-14069580 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):3 | ||||
chr17:14300747-14301111 | Common:3; Rare:96 | ||||
chr17:15262505-15262698 | Rare:49 | ||||
chr17:15684273-15684348 | Common:1; Rare:27 | ||||
chr17:15699514-15699773 | Common:3; Rare:68 | ||||
chr17:15999590-16000028 | Common:3; Rare:185; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
chr17:16217109-16217247 | Rare:44; Clinvar:1 | ||||
chr17:16380558-16381163 | Common:7; Rare:193 | ||||
chr17:17591567-17591926 | Common:2; Rare:106 | ||||
chr17:18039073-18039365 | Common:3; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
chr17:18087805-18088026 | Rare:60 | ||||
chr17:18183322-18183481 | Rare:35 |