| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:146544850-146544960 | Rare:31 | ||||
| chr3:148991442-148991611 | Common:2; Rare:76; Clinvar (benign):1 | ||||
| chr3:149129542-149129735 | Common:1; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149812572-149812762 | Common:1; Rare:53 | ||||
| chr3:149813577-149813859 | Common:1; Rare:51 | ||||
| chr3:150408090-150408367 | Common:2; Rare:103 | ||||
| chr3:150603181-150603309 | Common:1; Rare:41 | ||||
| chr3:151384745-151384992 | Common:1; Rare:42 | ||||
| chr3:152269575-152269703 | Rare:32 | ||||
| chr3:156674362-156674635 | Common:3; Rare:80 | ||||
| chr3:156826029-156826380 | Common:3; Rare:96 | ||||
| chr3:157149620-157149674 | Rare:6 | ||||
| chr3:157159448-157159608 | Common:3; Rare:65 | ||||
| chr3:157160133-157160296 | Rare:67 | ||||
| chr3:158571020-158571241 | Common:1; Rare:71 |