| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:78811300-78812303 | Common:7; Rare:452 | ||||
| chr15:78872205-78872369 | Common:5; Rare:53 | ||||
| chr15:78872293-78873950 | Common:65; Rare:2059 | ||||
| chr15:78926596-78926996 | Common:6; Rare:96 | ||||
| chr15:78937098-78937900 | Common:14; Rare:557 | ||||
| chr15:78944903-78945303 | Common:47; Rare:558 | ||||
| chr15:79310760-79311410 | Common:16; Rare:476 | ||||
| chr15:79311480-79311905 | Common:2; Rare:155 | ||||
| chr15:79896470-79896898 | Common:27; Rare:388; Clinvar (pathogenic):1 | ||||
| chr15:79896928-79897280 | Common:24; Rare:609 | ||||
| chr15:79897332-79897732 | Common:6; Rare:150 | ||||
| chr15:79922936-79923368 | Common:24; Rare:989 | ||||
| chr15:79923630-79924150 | Common:48; Rare:951 | ||||
| chr15:79970368-79971298 | Common:10; Rare:361 | ||||
| chr15:80058930-80059757 | Common:9; Rare:682 |