Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:8249197-8249317 | Common:1; Rare:34 | ||||
chr17:8965709-8965789 | Common:1; Rare:25 | ||||
chr17:9576591-9576666 | Rare:20 | ||||
chr17:10697461-10697654 | Common:3; Rare:90; Clinvar:5; Clinvar (benign):4 | ||||
chr17:10729754-10729816 | Rare:33 | ||||
chr17:10729972-10730128 | Common:3; Rare:34 | ||||
chr17:11997444-11997584 | Rare:49 | ||||
chr17:14069368-14069587 | Common:2; Rare:83; Clinvar:4; Clinvar (benign):3 | ||||
chr17:14300830-14301105 | Common:2; Rare:77 | ||||
chr17:15260740-15260996 | Common:2; Rare:87; Clinvar (benign):4 | ||||
chr17:15699547-15699797 | Common:3; Rare:70 | ||||
chr17:15999593-16000003 | Common:3; Rare:182; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
chr17:16039597-16039790 | Common:1; Rare:45 | ||||
chr17:16217073-16217235 | Rare:41; Clinvar:1 | ||||
chr17:16380577-16380829 | Common:4; Rare:66 |