| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:33194694-33194984 | Common:1; Rare:83 | ||||
| chr15:33310647-33310775 | Common:1; Rare:42 | ||||
| chr15:34101835-34102117 | Common:1; Rare:58 | ||||
| chr15:34209973-34210163 | Common:1; Rare:77 | ||||
| chr15:34224960-34225181 | Rare:84 | ||||
| chr15:34337551-34337839 | Common:1; Rare:82 | ||||
| chr15:34338028-34338077 | Rare:21 | ||||
| chr15:34343075-34343574 | Common:5; Rare:104; Clinvar:2; Clinvar (benign):1 | ||||
| chr15:34437396-34437685 | Common:1; Rare:64 | ||||
| chr15:34582813-34582904 | Rare:28 | ||||
| chr15:34583519-34583784 | Common:5; Rare:89 | ||||
| chr15:34588415-34588565 | Rare:44 | ||||
| chr15:34988169-34988306 | Common:2; Rare:48 | ||||
| chr15:34988757-34988792 | Rare:9 | ||||
| chr15:35546061-35546263 | Common:1; Rare:81 |