| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:16082567-16082743 | Common:2; Rare:38 | ||||
| chr4:16082919-16083198 | Common:1; Rare:61 | ||||
| chr4:16083265-16083457 | Common:3; Rare:46 | ||||
| chr4:16083561-16083807 | Common:2; Rare:58 | ||||
| chr4:16225792-16226082 | Common:2; Rare:83 | ||||
| chr4:16226455-16226669 | Common:3; Rare:83 | ||||
| chr4:17510928-17511967 | Common:11; Rare:318; Clinvar (benign):2 | ||||
| chr4:17512034-17512300 | Common:3; Rare:100; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr4:17577281-17577550 | Common:1; Rare:125 | ||||
| chr4:17614180-17614321 | Rare:30 | ||||
| chr4:17614544-17614679 | Common:2; Rare:71 | ||||
| chr4:17810652-17811043 | Common:4; Rare:124 | ||||
| chr4:18020544-18021194 | Common:5; Rare:263 | ||||
| chr4:18022050-18022390 | Common:4; Rare:94 | ||||
| chr4:20252735-20252935 | Common:1; Rare:48 |