Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:20413422-20413528 | Common:2; Rare:29 | ||||
chr14:20454772-20455295 | Common:7; Rare:137 | ||||
chr14:20684471-20684608 | Common:1; Rare:20; Clinvar (benign):1 | ||||
chr14:20989689-20989997 | Common:7; Rare:62 | ||||
chr14:21476946-21477267 | Common:1; Rare:94 | ||||
chr14:21511300-21511549 | Rare:63 | ||||
chr14:22589150-22589501 | Common:4; Rare:110 | ||||
chr14:22766560-22766699 | Common:1; Rare:74 | ||||
chr14:22929348-22929609 | Rare:61 | ||||
chr14:22976829-22976999 | Rare:31 | ||||
chr14:22982590-22982708 | Rare:41 | ||||
chr14:23095099-23095324 | Common:1; Rare:119 | ||||
chr14:23095440-23095572 | Common:2; Rare:55 | ||||
chr14:23286042-23286304 | Rare:77 | ||||
chr14:23306678-23306879 | Common:1; Rare:46 |