| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:88759447-88759542 | Rare:18 | ||||
| chr4:89111371-89111604 | Common:3; Rare:91 | ||||
| chr4:94451789-94451995 | Common:3; Rare:66 | ||||
| chr4:95549001-95549324 | Common:2; Rare:68 | ||||
| chr4:98143459-98143641 | Common:1; Rare:45 | ||||
| chr4:98261152-98261497 | Common:1; Rare:107 | ||||
| chr4:98929077-98929203 | Common:3; Rare:40 | ||||
| chr4:98995515-98995781 | Common:5; Rare:88 | ||||
| chr4:99088689-99088891 | Common:6; Rare:98 | ||||
| chr4:99144283-99144327 | Rare:8 | ||||
| chr4:99563510-99563763 | Common:2; Rare:67 | ||||
| chr4:99563931-99564165 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99894351-99894620 | Common:3; Rare:93 | ||||
| chr4:99946551-99946759 | Rare:76 | ||||
| chr4:99950166-99950511 | Common:1; Rare:89 |