| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56436037-56436327 | Rare:106 | ||||
| chr4:56467515-56467742 | Common:2; Rare:90; Clinvar (benign):5 | ||||
| chr4:56656301-56656543 | Common:3; Rare:41 | ||||
| chr4:56656546-56656720 | Common:1; Rare:33 | ||||
| chr4:56681236-56681480 | Common:1; Rare:37 | ||||
| chr4:56977231-56977283 | Rare:16 | ||||
| chr4:56977545-56977785 | Common:2; Rare:90 | ||||
| chr4:67545423-67545746 | Common:2; Rare:83 | ||||
| chr4:67701051-67701419 | Common:4; Rare:168 | ||||
| chr4:67883924-67884063 | Rare:38 | ||||
| chr4:68129813-68130251 | Common:2; Rare:70 | ||||
| chr4:68245520-68245838 | Rare:76 | ||||
| chr4:70688182-70688594 | Common:2; Rare:104 | ||||
| chr4:70704582-70704809 | Common:1; Rare:71 | ||||
| chr4:70902221-70902402 | Common:4; Rare:61 |