| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:24912788-24913100 | Common:3; Rare:223 | ||||
| chr4:25159852-25160176 | Common:3; Rare:127 | ||||
| chr4:25160274-25160827 | Common:11; Rare:371; Clinvar:6; Clinvar (benign):3 | ||||
| chr4:25233755-25234142 | Rare:353 | ||||
| chr4:25312569-25312913 | Common:8; Rare:254 | ||||
| chr4:25376912-25377372 | Common:11; Rare:364 | ||||
| chr4:25862016-25862196 | Common:1; Rare:42 | ||||
| chr4:25862729-25863062 | Common:1; Rare:122 | ||||
| chr4:25914038-25914552 | Common:6; Rare:266 | ||||
| chr4:25914580-25914890 | Common:3; Rare:53 | ||||
| chr4:26319290-26319868 | Rare:347 | ||||
| chr4:26320578-26321100 | Common:2; Rare:420; Clinvar (benign):3 | ||||
| chr4:26321090-26321522 | Common:8; Rare:295 | ||||
| chr4:26583961-26584152 | Rare:75 | ||||
| chr4:26857395-26857883 | Common:12; Rare:316 |