| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:92965976-92966179 | Rare:37 | ||||
| chr8:93698491-93698595 | Rare:20 | ||||
| chr8:93700404-93700660 | Common:1; Rare:98 | ||||
| chr8:93740925-93741202 | Common:1; Rare:88 | ||||
| chr8:93754773-93754941 | Common:1; Rare:62; Clinvar (benign):5 | ||||
| chr8:93916619-93916982 | Common:6; Rare:124; Clinvar (benign):1 | ||||
| chr8:94262296-94262456 | Rare:44 | ||||
| chr8:94436641-94436694 | Rare:20 | ||||
| chr8:94436907-94437036 | Rare:30 | ||||
| chr8:94553436-94553777 | Common:3; Rare:120 | ||||
| chr8:94719772-94720147 | Common:4; Rare:111 | ||||
| chr8:94895197-94895324 | Rare:41 | ||||
| chr8:94949362-94949548 | Common:1; Rare:56 | ||||
| chr8:95024754-95025190 | Common:2; Rare:144; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr8:95269191-95269303 | Common:5; Rare:47; Clinvar:1 |