| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:34224850-34225196 | Rare:114 | ||||
| chr15:34336955-34337135 | Common:2; Rare:38 | ||||
| chr15:34338042-34338206 | Common:1; Rare:51 | ||||
| chr15:34343065-34343255 | Common:4; Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
| chr15:34363419-34363684 | Rare:61 | ||||
| chr15:34365666-34365742 | Rare:23 | ||||
| chr15:34366610-34366624 | Rare:2 | ||||
| chr15:34366986-34367304 | Rare:115 | ||||
| chr15:34582754-34582894 | Rare:41 | ||||
| chr15:35546140-35546258 | Common:1; Rare:41 | ||||
| chr15:36579512-36579796 | Common:4; Rare:77 | ||||
| chr15:37094526-37094643 | Rare:19; Clinvar (benign):1 | ||||
| chr15:37098617-37099039 | Common:2; Rare:99 | ||||
| chr15:37099148-37099357 | Rare:55 | ||||
| chr15:37099851-37100018 | Rare:28 |