| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:142888938-142889056 | Common:2; Rare:27 | ||||
| chr3:142963305-142963662 | Common:1; Rare:93 | ||||
| chr3:142963985-142964078 | Common:2; Rare:25 | ||||
| chr3:143001472-143001646 | Common:2; Rare:64 | ||||
| chr3:143971689-143971825 | Common:1; Rare:65 | ||||
| chr3:143971961-143972074 | Rare:43 | ||||
| chr3:146160975-146161302 | Common:1; Rare:109; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:146544475-146544792 | Common:4; Rare:76 | ||||
| chr3:148991361-148991626 | Common:5; Rare:114; Clinvar (benign):1 | ||||
| chr3:149129549-149129676 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:149377637-149377851 | Common:1; Rare:52 | ||||
| chr3:149657948-149658191 | Rare:51 | ||||
| chr3:149812992-149813299 | Common:2; Rare:102 | ||||
| chr3:150408014-150408361 | Common:2; Rare:114 | ||||
| chr3:150408587-150408646 | Rare:21 |