| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:114132492-114132889 | Common:2; Rare:126 | ||||
| chr13:114281298-114281729 | Common:5; Rare:184 | ||||
| chr13:114281850-114282018 | Common:4; Rare:80 | ||||
| chr13:114282268-114282440 | Common:2; Rare:46 | ||||
| chr13:114285729-114285957 | Rare:39 | ||||
| chr13:114314217-114314647 | Common:1; Rare:130 | ||||
| chr14:20343398-20343680 | Common:7; Rare:148 | ||||
| chr14:20459597-20459841 | Common:2; Rare:57 | ||||
| chr14:20461733-20462016 | Common:2; Rare:68 | ||||
| chr14:20684423-20684628 | Common:2; Rare:33; Clinvar (benign):2 | ||||
| chr14:21211555-21211883 | Common:3; Rare:84 | ||||
| chr14:21262879-21263049 | Rare:25 | ||||
| chr14:21269533-21269905 | Common:4; Rare:130 | ||||
| chr14:21437202-21437408 | Common:4; Rare:87 | ||||
| chr14:21476611-21476766 | Rare:70 |