| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:114282124-114282216 | Common:1; Rare:35 | ||||
| chr13:114282414-114282552 | Common:1; Rare:36 | ||||
| chr13:114314160-114314596 | Common:3; Rare:131 | ||||
| chr13:114314687-114314811 | Rare:35 | ||||
| chr14:20305897-20306074 | Common:1; Rare:58 | ||||
| chr14:20333249-20333399 | Common:1; Rare:30 | ||||
| chr14:20343086-20343774 | Common:13; Rare:373 | ||||
| chr14:20412971-20413350 | Common:4; Rare:62 | ||||
| chr14:20413365-20413634 | Common:5; Rare:70 | ||||
| chr14:20413917-20414019 | Rare:23 | ||||
| chr14:20454514-20454657 | Rare:49 | ||||
| chr14:20454696-20455380 | Common:7; Rare:184 | ||||
| chr14:20460450-20460690 | Rare:57 | ||||
| chr14:20461728-20462045 | Common:3; Rare:77 | ||||
| chr14:20469247-20469513 | Common:2; Rare:59; Clinvar:2; Clinvar (benign):1 |