| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96208248-96208616 | Common:2; Rare:154 | ||||
| chr2:96208772-96208979 | Common:4; Rare:85 | ||||
| chr2:96265972-96266362 | Common:2; Rare:116; Clinvar:1 | ||||
| chr2:96305433-96305638 | Common:2; Rare:79; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:96325228-96325353 | Rare:33 | ||||
| chr2:96335697-96335819 | Common:1; Rare:42 | ||||
| chr2:96638282-96638467 | Common:1; Rare:47 | ||||
| chr2:96857888-96858225 | Common:2; Rare:120 | ||||
| chr2:96868509-96868778 | Rare:68 | ||||
| chr2:96869890-96870161 | Common:2; Rare:57 | ||||
| chr2:96870810-96870856 | Rare:9 | ||||
| chr2:96986529-96986750 | Rare:87 | ||||
| chr2:97094815-97094996 | Common:1; Rare:41 | ||||
| chr2:97113464-97113678 | Rare:49 | ||||
| chr2:97589825-97589986 | Common:4; Rare:33 |