| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:94451786-94451993 | Common:3; Rare:65 | ||||
| chr4:95549205-95549334 | Common:1; Rare:23 | ||||
| chr4:98143450-98143619 | Common:1; Rare:39 | ||||
| chr4:98261194-98261522 | Common:1; Rare:108 | ||||
| chr4:98929093-98929378 | Common:3; Rare:74 | ||||
| chr4:98995470-98995773 | Common:6; Rare:108 | ||||
| chr4:99088689-99088879 | Common:6; Rare:91 | ||||
| chr4:99144196-99144413 | Common:1; Rare:36 | ||||
| chr4:99321311-99321553 | Rare:53 | ||||
| chr4:99352661-99352917 | Rare:56 | ||||
| chr4:99563593-99563812 | Common:2; Rare:70 | ||||
| chr4:99563965-99564170 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99894357-99894593 | Common:2; Rare:86 | ||||
| chr4:99950251-99950510 | Rare:52 | ||||
| chr4:101347519-101347840 | Common:5; Rare:97 |