| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:36328586-36328968 | Rare:88 | ||||
| chr22:36387705-36388468 | Common:7; Rare:202; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:36481299-36481445 | Common:2; Rare:31 | ||||
| chr22:36481520-36481759 | Common:2; Rare:68 | ||||
| chr22:36481920-36482291 | Common:2; Rare:92 | ||||
| chr22:36506999-36507274 | Common:5; Rare:103 | ||||
| chr22:36528865-36529642 | Common:9; Rare:239 | ||||
| chr22:36529701-36529887 | Rare:39 | ||||
| chr22:36776000-36776336 | Common:2; Rare:82 | ||||
| chr22:36776509-36776618 | Common:1; Rare:34 | ||||
| chr22:36860806-36861483 | Common:2; Rare:158; Clinvar:1; Clinvar (benign):2 | ||||
| chr22:36913320-36913650 | Common:2; Rare:61 | ||||
| chr22:36913899-36914299 | Common:6; Rare:82 | ||||
| chr22:36921533-36921691 | Rare:29 | ||||
| chr22:37019411-37019542 | Common:1; Rare:42 |