| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:113001485-113001772 | Common:1; Rare:60 | ||||
| chr13:113208630-113208751 | Rare:69 | ||||
| chr13:113364103-113364463 | Common:2; Rare:24 | ||||
| chr13:113490683-113491021 | Common:1; Rare:122 | ||||
| chr13:113584466-113584712 | Rare:71 | ||||
| chr13:114281548-114281654 | Common:1; Rare:59 | ||||
| chr13:114281787-114282090 | Common:6; Rare:154 | ||||
| chr14:20343184-20343666 | Common:12; Rare:285 | ||||
| chr14:20413420-20413531 | Common:3; Rare:31 | ||||
| chr14:20454754-20454795 | Rare:10 | ||||
| chr14:20454804-20455324 | Common:7; Rare:135 | ||||
| chr14:20684479-20684644 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chr14:20989749-20990005 | Common:4; Rare:53 | ||||
| chr14:21025043-21025288 | Rare:82 | ||||
| chr14:21025437-21025622 | Common:1; Rare:44 |