| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15469866-15469917 | Rare:7 | ||||
| chr4:15655223-15655494 | Common:2; Rare:108 | ||||
| chr4:15681458-15681869 | Common:3; Rare:142 | ||||
| chr4:15702995-15703128 | Common:1; Rare:27 | ||||
| chr4:16898555-16898874 | Common:14; Rare:57 | ||||
| chr4:17614548-17614669 | Common:2; Rare:56 | ||||
| chr4:17810681-17810990 | Common:1; Rare:94 | ||||
| chr4:20700329-20700548 | Common:3; Rare:92 | ||||
| chr4:24584459-24584716 | Common:1; Rare:81 | ||||
| chr4:25160388-25160727 | Common:3; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233841-25234078 | Rare:99 | ||||
| chr4:25376984-25377379 | Common:3; Rare:123 | ||||
| chr4:25914034-25914337 | Common:3; Rare:132 | ||||
| chr4:26320592-26320832 | Common:1; Rare:92 | ||||
| chr4:26320908-26321043 | Rare:48; Clinvar (benign):1 |