| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:45378537-45378643 | Common:2; Rare:28 | ||||
| chr15:45587093-45587246 | Rare:26 | ||||
| chr15:45587281-45587618 | Common:1; Rare:113; Clinvar:7; Clinvar (benign):3 | ||||
| chr15:45587661-45587844 | Common:2; Rare:56 | ||||
| chr15:48331367-48331453 | Rare:27 | ||||
| chr15:48331885-48332243 | Common:7; Rare:108 | ||||
| chr15:48645706-48645881 | Common:2; Rare:57; Clinvar (benign):1 | ||||
| chr15:48645996-48646132 | Common:1; Rare:43 | ||||
| chr15:48878038-48878188 | Rare:57 | ||||
| chr15:49155570-49155842 | Common:2; Rare:92 | ||||
| chr15:49620752-49621129 | Common:6; Rare:140 | ||||
| chr15:50119231-50119382 | Rare:24 | ||||
| chr15:50354840-50354999 | Rare:26 | ||||
| chr15:50355093-50355528 | Common:3; Rare:180 | ||||
| chr15:50424155-50424466 | Common:2; Rare:115 |