| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103562273-103562375 | Rare:36 | ||||
| chr14:103562624-103563053 | Common:8; Rare:170; Clinvar (benign):5 | ||||
| chr14:103715437-103715853 | Common:1; Rare:140 | ||||
| chr14:104970477-104970583 | Common:3; Rare:20 | ||||
| chr15:25438984-25439121 | Common:2; Rare:52 | ||||
| chr15:29269779-29269837 | Rare:23 | ||||
| chr15:31870637-31870885 | Rare:77 | ||||
| chr15:32615099-32615459 | Common:3; Rare:93 | ||||
| chr15:34101821-34102083 | Common:1; Rare:59 | ||||
| chr15:34582823-34582890 | Rare:19 | ||||
| chr15:35546137-35546263 | Common:1; Rare:44 | ||||
| chr15:36579547-36579732 | Common:2; Rare:51 | ||||
| chr15:37100366-37100775 | Common:1; Rare:130 | ||||
| chr15:37101280-37101323 | Common:1; Rare:10 | ||||
| chr15:38252795-38252854 | Rare:14 |