| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:89111407-89111630 | Common:2; Rare:78 | ||||
| chr4:94207497-94207716 | Common:2; Rare:63 | ||||
| chr4:94451789-94451987 | Common:3; Rare:62 | ||||
| chr4:98261155-98261559 | Common:1; Rare:136 | ||||
| chr4:98378911-98379093 | Rare:35 | ||||
| chr4:98657135-98657409 | Common:2; Rare:53 | ||||
| chr4:98657616-98657830 | Rare:41 | ||||
| chr4:98658155-98658375 | Common:1; Rare:54 | ||||
| chr4:98658377-98658453 | Rare:13 | ||||
| chr4:98658560-98658946 | Common:2; Rare:112 | ||||
| chr4:98891234-98891495 | Rare:48 | ||||
| chr4:98929083-98929360 | Common:3; Rare:72 | ||||
| chr4:99088691-99088941 | Common:7; Rare:114 | ||||
| chr4:99563608-99563815 | Common:2; Rare:64 | ||||
| chr4:99563993-99564148 | Common:2; Rare:49; Clinvar:2; Clinvar (benign):2 |