| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:77421058-77421237 | Rare:82 | ||||
| chr15:78131290-78131740 | Common:4; Rare:183 | ||||
| chr15:78149123-78149416 | Common:2; Rare:190 | ||||
| chr15:78299547-78299823 | Common:2; Rare:183 | ||||
| chr15:78437940-78438335 | Common:7; Rare:294 | ||||
| chr15:78507257-78507628 | Rare:185 | ||||
| chr15:78540346-78540497 | Common:5; Rare:98 | ||||
| chr15:78540540-78540830 | Common:4; Rare:161 | ||||
| chr15:78872650-78873077 | Common:12; Rare:255 | ||||
| chr15:78944946-78945271 | Common:20; Rare:248 | ||||
| chr15:79896468-79896932 | Common:15; Rare:277; Clinvar (pathogenic):1 | ||||
| chr15:79896969-79897131 | Common:4; Rare:119 | ||||
| chr15:79923050-79923177 | Common:1; Rare:57 | ||||
| chr15:79923645-79923988 | Common:13; Rare:253 | ||||
| chr15:80059424-80059783 | Common:2; Rare:225 |