Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:150176322-150176457 | Rare:22 | ||||
chr6:150176833-150176994 | Common:1; Rare:30 | ||||
chr6:152380442-152380555 | Common:1; Rare:19 | ||||
chr6:158043784-158043921 | Rare:29 | ||||
chr6:158627203-158627458 | Common:1; Rare:56 | ||||
chr6:158776406-158776732 | Rare:80; Clinvar:1; Clinvar (benign):2 | ||||
chr6:162234614-162234850 | Common:6; Rare:39 | ||||
chr6:170165671-170165824 | Common:2; Rare:28 | ||||
chr7:522406-522630 | Common:2; Rare:48 | ||||
chr7:711501-711569 | Rare:23 | ||||
chr7:2009068-2009273 | Common:2; Rare:60 | ||||
chr7:5427815-5427881 | Rare:28 | ||||
chr7:5695459-5695737 | Common:3; Rare:62 | ||||
chr7:5703301-5703431 | Rare:30 | ||||
chr7:15688173-15688420 | Common:2; Rare:67 |