Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:29752581-29752759 | Common:3; Rare:26 | ||||
chr6:29964906-29965108 | Common:15; Rare:35 | ||||
chr6:31196187-31196411 | Common:3; Rare:50 | ||||
chr6:31400599-31400722 | Common:4; Rare:27 | ||||
chr6:31822066-31822281 | Common:2; Rare:41 | ||||
chr6:31978961-31979282 | Common:5; Rare:51 | ||||
chr6:32028697-32029061 | Common:1; Rare:77 | ||||
chr6:32894636-32894807 | Common:2; Rare:47 | ||||
chr6:32980454-32980719 | Common:8; Rare:123 | ||||
chr6:33425656-33425854 | Common:1; Rare:49; Clinvar (benign):1 | ||||
chr6:33906464-33906740 | Common:2; Rare:65 | ||||
chr6:35729126-35729348 | Rare:34 | ||||
chr6:35729438-35729793 | Rare:46 | ||||
chr6:36118643-36118683 | Rare:6 | ||||
chr6:41041271-41041421 | Rare:22 |