| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:89836528-89837669 | Common:17; Rare:512; Clinvar:12; Clinvar (benign):3 | ||||
| chr4:94207360-94207690 | Common:3; Rare:184 | ||||
| chr4:94207710-94207960 | Common:1; Rare:179 | ||||
| chr4:94207910-94208310 | Common:3; Rare:297 | ||||
| chr4:94342677-94343077 | Rare:127 | ||||
| chr4:94451632-94452032 | Common:18; Rare:461 | ||||
| chr4:94454614-94455407 | Common:8; Rare:178 | ||||
| chr4:98143254-98143737 | Common:5; Rare:321 | ||||
| chr4:98260718-98260960 | Rare:63 | ||||
| chr4:98261026-98261635 | Common:15; Rare:883 | ||||
| chr4:98261968-98262614 | Common:2; Rare:146 | ||||
| chr4:98658483-98658896 | Common:15; Rare:478 | ||||
| chr4:98891701-98892213 | Rare:138 | ||||
| chr4:98928298-98929554 | Common:31; Rare:1144 | ||||
| chr4:98929504-98929944 | Common:2; Rare:132 |