| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:8269554-8269757 | Common:1; Rare:75 | ||||
| chr4:8440715-8441011 | Rare:113 | ||||
| chr4:10116687-10117089 | Common:8; Rare:190 | ||||
| chr4:15427855-15428096 | Rare:33 | ||||
| chr4:15469606-15469903 | Common:1; Rare:59 | ||||
| chr4:15478924-15479283 | Common:2; Rare:76 | ||||
| chr4:15655289-15655494 | Common:1; Rare:93 | ||||
| chr4:15681474-15681869 | Common:3; Rare:136 | ||||
| chr4:15702967-15703108 | Common:2; Rare:28 | ||||
| chr4:16898400-16898462 | Rare:16 | ||||
| chr4:17614548-17614651 | Common:2; Rare:44 | ||||
| chr4:17810658-17810993 | Common:2; Rare:106 | ||||
| chr4:25160382-25160710 | Common:3; Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233853-25234058 | Rare:88 | ||||
| chr4:25914051-25914291 | Common:2; Rare:103 |