| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:99894344-99894620 | Common:3; Rare:96 | ||||
| chr4:99946545-99946874 | Rare:115 | ||||
| chr4:99950248-99950532 | Rare:63 | ||||
| chr4:102826760-102826986 | Rare:64 | ||||
| chr4:102827096-102827603 | Common:1; Rare:189 | ||||
| chr4:102827687-102827980 | Common:3; Rare:86 | ||||
| chr4:102827985-102828301 | Common:3; Rare:107 | ||||
| chr4:102868850-102869063 | Common:2; Rare:72 | ||||
| chr4:103076302-103076378 | Rare:25 | ||||
| chr4:105708645-105708845 | Common:1; Rare:64 | ||||
| chr4:106316151-106316617 | Common:5; Rare:152 | ||||
| chr4:107720175-107720436 | Common:6; Rare:106 | ||||
| chr4:107824451-107824736 | Common:1; Rare:60 | ||||
| chr4:107825587-107825718 | Common:1; Rare:16 | ||||
| chr4:107989689-107989900 | Common:5; Rare:101; Clinvar:4; Clinvar (benign):5 |