Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:40330288-40330614 | Common:1; Rare:52 | ||||
chr17:40331822-40331998 | Rare:37 | ||||
chr17:45150086-45150302 | Rare:82 | ||||
chr17:45222799-45222937 | Common:1; Rare:30 | ||||
chr17:45223245-45223399 | Common:1; Rare:28 | ||||
chr17:45223759-45224009 | Rare:50 | ||||
chr17:45226109-45226417 | Common:1; Rare:67 | ||||
chr17:45228996-45229104 | Common:1; Rare:14 | ||||
chr17:45583444-45583769 | Common:8; Rare:25 | ||||
chr17:46031611-46031793 | Rare:50; Clinvar:3; Clinvar (benign):6 | ||||
chr17:49217266-49217306 | Rare:10 | ||||
chr17:49218890-49218966 | Common:2; Rare:13 | ||||
chr17:50148528-50148787 | Rare:50 | ||||
chr17:50646176-50646360 | Common:2; Rare:34 | ||||
chr17:50741439-50741712 | Common:2; Rare:67 |