Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:34101843-34102060 | Rare:44 | ||||
chr15:35546141-35546252 | Common:1; Rare:39 | ||||
chr15:40039096-40039329 | Rare:98 | ||||
chr15:40695076-40695214 | Rare:39 | ||||
chr15:40807450-40807761 | Common:4; Rare:104 | ||||
chr15:40844366-40844631 | Rare:97 | ||||
chr15:41417028-41417169 | Common:1; Rare:60 | ||||
chr15:42273400-42273527 | Rare:48 | ||||
chr15:42548774-42548874 | Common:1; Rare:59 | ||||
chr15:43330574-43330674 | Rare:36 | ||||
chr15:43371043-43371081 | Rare:3 | ||||
chr15:43746606-43746632 | Rare:7 | ||||
chr15:44537045-44537215 | Common:1; Rare:67 | ||||
chr15:45129915-45130002 | Rare:21 | ||||
chr15:45587102-45587432 | Common:1; Rare:81; Clinvar:6; Clinvar (benign):1 |