| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:674226-674585 | Common:3; Rare:167 | ||||
| chr4:705593-705955 | Common:1; Rare:124 | ||||
| chr4:932245-932520 | Common:2; Rare:109 | ||||
| chr4:986900-987146 | Common:3; Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:987260-987520 | Rare:70 | ||||
| chr4:1289640-1289942 | Common:1; Rare:109 | ||||
| chr4:1720528-1720608 | Rare:18 | ||||
| chr4:2041885-2042068 | Common:1; Rare:69 | ||||
| chr4:2468871-2469200 | Common:5; Rare:133 | ||||
| chr4:2843667-2844022 | Common:3; Rare:128 | ||||
| chr4:2926670-2926842 | Common:2; Rare:46 | ||||
| chr4:2934777-2934947 | Common:4; Rare:80 | ||||
| chr4:2963309-2963611 | Common:2; Rare:114 | ||||
| chr4:2963830-2963916 | Common:2; Rare:18 | ||||
| chr4:3074516-3074700 | Common:4; Rare:59 |