| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143931935-143932189 | Common:2; Rare:132; Clinvar:8; Clinvar (benign):7 | ||||
| chr8:143937037-143937346 | Common:2; Rare:110; Clinvar:6; Clinvar (benign):4 | ||||
| chr8:144316633-144316890 | Rare:106; Clinvar (pathogenic):1 | ||||
| chr8:145002827-145003047 | Common:2; Rare:77 | ||||
| chr9:684204-684325 | Common:2; Rare:32 | ||||
| chr9:686524-686847 | Common:4; Rare:85 | ||||
| chr9:15468933-15469391 | Common:2; Rare:141 | ||||
| chr9:15479622-15479913 | Common:2; Rare:88 | ||||
| chr9:15486039-15486274 | Common:1; Rare:66 | ||||
| chr9:15486825-15487056 | Common:2; Rare:68 | ||||
| chr9:25677404-25677681 | Common:3; Rare:115 | ||||
| chr9:33026278-33026593 | Common:2; Rare:84 | ||||
| chr9:35491061-35491307 | Common:2; Rare:47 | ||||
| chr9:35491933-35492251 | Common:1; Rare:47 | ||||
| chr9:35683319-35683589 | Common:2; Rare:41 |