| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:40749857-40750223 | Common:2; Rare:97 | ||||
| chr4:41256733-41256954 | Common:2; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:41935057-41935256 | Common:3; Rare:59 | ||||
| chr4:41990362-41990572 | Common:1; Rare:73 | ||||
| chr4:44678369-44678547 | Common:1; Rare:60 | ||||
| chr4:44678598-44678750 | Rare:68 | ||||
| chr4:44726487-44726662 | Common:2; Rare:66 | ||||
| chr4:46993538-46993673 | Common:2; Rare:37 | ||||
| chr4:47463605-47463792 | Common:2; Rare:72 | ||||
| chr4:47485204-47485397 | Common:2; Rare:65 | ||||
| chr4:47837469-47837530 | Rare:7 | ||||
| chr4:47837704-47837990 | Common:1; Rare:90; Clinvar:1 | ||||
| chr4:47837999-47838215 | Common:1; Rare:39 | ||||
| chr4:48016607-48016795 | Common:1; Rare:56 | ||||
| chr4:48269784-48269996 | Common:2; Rare:50 |