Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:39588325-39588711 | Common:3; Rare:91; Clinvar (benign):2 | ||||
chr15:39589132-39589274 | Common:1; Rare:36 | ||||
chr15:39592635-39593226 | Common:1; Rare:125; Clinvar (benign):1 | ||||
chr15:39782794-39782872 | Rare:22 | ||||
chr15:39934051-39934187 | Common:3; Rare:47 | ||||
chr15:40038864-40039349 | Common:1; Rare:172 | ||||
chr15:40695050-40695162 | Rare:31 | ||||
chr15:40763781-40764130 | Common:3; Rare:82 | ||||
chr15:40807444-40807761 | Common:4; Rare:104 | ||||
chr15:41115982-41116030 | Rare:17 | ||||
chr15:41402450-41402554 | Common:2; Rare:34 | ||||
chr15:41416982-41417296 | Common:3; Rare:118 | ||||
chr15:41660309-41660488 | Rare:61 | ||||
chr15:41827922-41828165 | Common:4; Rare:91 | ||||
chr15:41893918-41894045 | Rare:25 |