| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141486867-141487074 | Common:1; Rare:64 | ||||
| chr3:141738093-141738418 | Common:2; Rare:136 | ||||
| chr3:141876048-141876246 | Rare:55 | ||||
| chr3:141876439-141876829 | Common:3; Rare:166 | ||||
| chr3:142225456-142225685 | Common:3; Rare:79 | ||||
| chr3:142447968-142448137 | Common:1; Rare:61 | ||||
| chr3:142578690-142578976 | Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142596262-142596496 | Common:3; Rare:58 | ||||
| chr3:142888879-142889297 | Common:4; Rare:92 | ||||
| chr3:143001385-143001654 | Common:3; Rare:101 | ||||
| chr3:143971689-143971825 | Common:1; Rare:65 | ||||
| chr3:143971967-143972074 | Rare:42 | ||||
| chr3:146160968-146161304 | Common:1; Rare:111; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:146544498-146544793 | Common:4; Rare:70 | ||||
| chr3:148991386-148991628 | Common:2; Rare:111; Clinvar (benign):1 |