| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39051936-39052056 | Common:1; Rare:44 | ||||
| chr3:39107555-39107681 | Common:2; Rare:40 | ||||
| chr3:39383324-39383437 | Common:2; Rare:22; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:40309486-40309816 | Common:9; Rare:114 | ||||
| chr3:40457204-40457370 | Common:2; Rare:79 | ||||
| chr3:40457590-40457990 | Common:4; Rare:118 | ||||
| chr3:40505932-40506125 | Rare:43 | ||||
| chr3:42149179-42149390 | Rare:52 | ||||
| chr3:42581913-42582137 | Common:3; Rare:69 | ||||
| chr3:42590693-42590918 | Common:3; Rare:68 | ||||
| chr3:42600377-42600757 | Common:2; Rare:146 | ||||
| chr3:42773215-42773334 | Common:1; Rare:34 | ||||
| chr3:42804427-42804671 | Common:2; Rare:76 | ||||
| chr3:43621902-43622152 | Common:2; Rare:91; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690809-43691004 | Common:3; Rare:108; Clinvar:7; Clinvar (benign):2 |