| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:107989646-107989983 | Common:6; Rare:147; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620354-108620646 | Common:6; Rare:147 | ||||
| chr4:109302361-109302397 | Rare:6 | ||||
| chr4:109302890-109303064 | Common:3; Rare:46 | ||||
| chr4:109433524-109433681 | Common:1; Rare:47 | ||||
| chr4:109433756-109433822 | Common:1; Rare:26 | ||||
| chr4:109703406-109703552 | Rare:53 | ||||
| chr4:109730045-109730202 | Common:2; Rare:31 | ||||
| chr4:109815458-109815833 | Common:1; Rare:96 | ||||
| chr4:112145291-112145678 | Common:2; Rare:102 | ||||
| chr4:112231586-112232009 | Common:3; Rare:122 | ||||
| chr4:112516536-112516850 | Common:2; Rare:87 | ||||
| chr4:112636844-112637181 | Rare:92 | ||||
| chr4:112637384-112637576 | Common:3; Rare:54 | ||||
| chr4:113049450-113049657 | Common:1; Rare:34 |