| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:42548702-42548912 | Common:2; Rare:111 | ||||
| chr15:43330543-43330737 | Common:1; Rare:72 | ||||
| chr15:43371030-43371108 | Rare:16 | ||||
| chr15:43746287-43746446 | Common:1; Rare:61 | ||||
| chr15:43824603-43824802 | Common:2; Rare:55 | ||||
| chr15:44427555-44427690 | Rare:40 | ||||
| chr15:44536663-44536733 | Rare:13 | ||||
| chr15:44536863-44537401 | Common:3; Rare:198 | ||||
| chr15:44711307-44711612 | Rare:91; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45023052-45023233 | Common:3; Rare:47 | ||||
| chr15:45201108-45201133 | Common:1; Rare:13 | ||||
| chr15:45587288-45587621 | Common:1; Rare:114; Clinvar:7; Clinvar (benign):3 | ||||
| chr15:47717149-47717474 | Common:1; Rare:65 | ||||
| chr15:47718383-47718487 | Rare:24 | ||||
| chr15:48645710-48645821 | Common:1; Rare:32; Clinvar (benign):1 |