Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:50765576-50765709 | Common:1; Rare:46 | ||||
chr15:50908574-50908765 | Common:2; Rare:79; Clinvar (benign):2 | ||||
chr15:51622597-51622928 | Rare:111 | ||||
chr15:51681387-51681837 | Common:2; Rare:118 | ||||
chr15:51751478-51751699 | Common:1; Rare:55 | ||||
chr15:51924275-51924291 | Rare:2 | ||||
chr15:51971732-51971841 | Rare:51 | ||||
chr15:52019098-52019279 | Common:1; Rare:92 | ||||
chr15:52179875-52180017 | Common:1; Rare:58 | ||||
chr15:55196848-55197013 | Common:4; Rare:56 | ||||
chr15:55318932-55318996 | Rare:20 | ||||
chr15:55319049-55319248 | Common:3; Rare:53 | ||||
chr15:55408020-55408107 | Common:1; Rare:23 | ||||
chr15:55408237-55408694 | Common:4; Rare:99 | ||||
chr15:55588411-55588639 | Common:1; Rare:72 |