| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:78299482-78299889 | Common:1; Rare:118 | ||||
| chr15:78437870-78438388 | Common:5; Rare:196 | ||||
| chr15:78507228-78507647 | Rare:107 | ||||
| chr15:78540251-78540966 | Common:8; Rare:208 | ||||
| chr15:78541517-78541661 | Rare:28 | ||||
| chr15:78564945-78565218 | Common:1; Rare:43 | ||||
| chr15:78565245-78565632 | Common:3; Rare:108 | ||||
| chr15:78811429-78811620 | Common:1; Rare:59 | ||||
| chr15:78872812-78873086 | Common:1; Rare:100 | ||||
| chr15:78873147-78873818 | Common:6; Rare:246 | ||||
| chr15:78944509-78944629 | Common:1; Rare:16 | ||||
| chr15:78944871-78945312 | Common:13; Rare:167 | ||||
| chr15:78978680-78978919 | Common:3; Rare:41 | ||||
| chr15:79310766-79311370 | Common:6; Rare:179 | ||||
| chr15:79896638-79896889 | Common:8; Rare:104; Clinvar (pathogenic):1 |