| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:105473351-105473646 | Common:1; Rare:118 | ||||
| chr4:105473704-105473798 | Common:1; Rare:37 | ||||
| chr4:105473882-105474213 | Common:5; Rare:141 | ||||
| chr4:105708432-105708902 | Common:4; Rare:128 | ||||
| chr4:105895254-105895493 | Rare:70 | ||||
| chr4:105895968-105896137 | Common:2; Rare:40 | ||||
| chr4:106315995-106316111 | Rare:24 | ||||
| chr4:106316163-106316689 | Common:5; Rare:163 | ||||
| chr4:107720108-107720709 | Common:9; Rare:232 | ||||
| chr4:107824629-107824738 | Rare:24 | ||||
| chr4:107824762-107825027 | Common:1; Rare:68 | ||||
| chr4:107931236-107931658 | Common:5; Rare:135; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr4:107989599-107989968 | Common:6; Rare:147; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108168622-108168893 | Common:2; Rare:62 | ||||
| chr4:108620388-108620685 | Common:6; Rare:142 |