| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56387409-56387553 | Rare:48 | ||||
| chr4:56435467-56435973 | Common:6; Rare:166 | ||||
| chr4:56435994-56436307 | Rare:111 | ||||
| chr4:56467515-56467689 | Common:2; Rare:74; Clinvar (benign):4 | ||||
| chr4:56977558-56977747 | Common:2; Rare:72 | ||||
| chr4:61202494-61202638 | Rare:33 | ||||
| chr4:65670293-65670617 | Common:1; Rare:86 | ||||
| chr4:65670684-65670719 | Rare:6 | ||||
| chr4:67545364-67545759 | Common:2; Rare:94 | ||||
| chr4:67701121-67701421 | Common:4; Rare:135 | ||||
| chr4:68349914-68350209 | Common:1; Rare:101 | ||||
| chr4:70688342-70688574 | Common:2; Rare:60 | ||||
| chr4:70839232-70839421 | Common:2; Rare:82 | ||||
| chr4:70902157-70902372 | Common:5; Rare:82 | ||||
| chr4:70993491-70993801 | Common:5; Rare:93 |