| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:79896605-79896853 | Common:7; Rare:100 | ||||
| chr15:79896926-79897246 | Common:4; Rare:110 | ||||
| chr15:79897252-79897384 | Common:1; Rare:26 | ||||
| chr15:79897441-79897474 | Common:1; Rare:6 | ||||
| chr15:79923035-79923354 | Common:4; Rare:130 | ||||
| chr15:79923407-79923509 | Rare:39 | ||||
| chr15:79923561-79924123 | Common:9; Rare:209 | ||||
| chr15:79924125-79924221 | Common:3; Rare:20 | ||||
| chr15:80059157-80059173 | Rare:2 | ||||
| chr15:80059352-80059792 | Common:1; Rare:147 | ||||
| chr15:80059847-80060077 | Common:1; Rare:86 | ||||
| chr15:80060115-80060317 | Common:2; Rare:72 | ||||
| chr15:80152425-80152878 | Common:10; Rare:33; Clinvar (benign):1 | ||||
| chr15:80152934-80153064 | Common:2; Rare:36; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:80694969-80695397 | Common:3; Rare:133 |