| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:101948063-101948388 | Common:1; Rare:95 | ||||
| chr14:106845631-106845811 | Common:1; Rare:46 | ||||
| chr14:106845820-106845883 | Common:1; Rare:20 | ||||
| chr15:23303481-23303775 | Rare:25 | ||||
| chr15:23686038-23686284 | Common:1; Rare:57; Clinvar (benign):1 | ||||
| chr15:28589208-28589516 | Common:1; Rare:10 | ||||
| chr15:28684019-28684179 | Common:2; Rare:14 | ||||
| chr15:29704239-29704513 | Common:1; Rare:61 | ||||
| chr15:29730406-29730611 | Rare:44 | ||||
| chr15:33148320-33148607 | Rare:51 | ||||
| chr15:36932365-36932638 | Common:1; Rare:42 | ||||
| chr15:41305043-41305105 | Rare:8 | ||||
| chr15:48258913-48259311 | Common:4; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr15:48298850-48299183 | Common:1; Rare:66 | ||||
| chr15:56443806-56443947 | Rare:38 |