| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:78565755-78565898 | Rare:35 | ||||
| chr15:78810424-78810577 | Rare:34 | ||||
| chr15:78811338-78811681 | Common:1; Rare:97 | ||||
| chr15:78944881-78944912 | Common:1; Rare:10 | ||||
| chr15:78944952-78945209 | Common:9; Rare:118 | ||||
| chr15:79311051-79311411 | Common:5; Rare:125 | ||||
| chr15:79311466-79311644 | Rare:39 | ||||
| chr15:79896481-79897384 | Common:13; Rare:291; Clinvar (pathogenic):1 | ||||
| chr15:79897451-79897521 | Common:1; Rare:19 | ||||
| chr15:79923038-79923380 | Common:4; Rare:143 | ||||
| chr15:79923412-79923495 | Rare:33 | ||||
| chr15:79923511-79924137 | Common:9; Rare:229 | ||||
| chr15:80059391-80059795 | Common:1; Rare:132 | ||||
| chr15:80059848-80060070 | Common:1; Rare:84 | ||||
| chr15:80060093-80060356 | Common:2; Rare:91 |