| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:139389568-139389868 | Common:1; Rare:96 | ||||
| chr3:139539587-139539783 | Common:1; Rare:64 | ||||
| chr3:140941657-140941878 | Common:2; Rare:84 | ||||
| chr3:141231623-141231888 | Common:2; Rare:91 | ||||
| chr3:141368260-141368548 | Rare:60 | ||||
| chr3:141386749-141386978 | Rare:33 | ||||
| chr3:141402267-141402425 | Common:2; Rare:47 | ||||
| chr3:142447968-142448137 | Common:1; Rare:61 | ||||
| chr3:142578708-142579037 | Rare:119; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:143001472-143001654 | Common:2; Rare:69 | ||||
| chr3:146161077-146161386 | Common:2; Rare:83; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:146544524-146544818 | Common:4; Rare:70 | ||||
| chr3:148991386-148991632 | Common:2; Rare:113; Clinvar (benign):1 | ||||
| chr3:149129549-149129714 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149658023-149658181 | Rare:38 |