| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:109560090-109560432 | Common:3; Rare:95 | ||||
| chr4:109815921-109816033 | Rare:19 | ||||
| chr4:112231570-112231825 | Common:2; Rare:82 | ||||
| chr4:112285757-112285961 | Rare:64 | ||||
| chr4:112636901-112637205 | Common:2; Rare:80 | ||||
| chr4:113761110-113761343 | Common:1; Rare:55 | ||||
| chr4:118685339-118685471 | Common:2; Rare:43 | ||||
| chr4:121801154-121801389 | Common:3; Rare:79 | ||||
| chr4:121870411-121870663 | Common:1; Rare:59; Clinvar (benign):1 | ||||
| chr4:129093451-129093760 | Common:1; Rare:89 | ||||
| chr4:139301334-139301531 | Common:2; Rare:62 | ||||
| chr4:139556435-139556569 | Rare:16 | ||||
| chr4:139556742-139556813 | Rare:13 | ||||
| chr4:140373384-140373696 | Common:2; Rare:126 | ||||
| chr4:143184657-143184957 | Common:8; Rare:118 |