| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96208795-96208950 | Common:3; Rare:63 | ||||
| chr2:96265953-96266348 | Common:2; Rare:120; Clinvar:2 | ||||
| chr2:96305449-96305618 | Common:2; Rare:61; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:96325258-96325376 | Rare:31 | ||||
| chr2:96335686-96335803 | Common:1; Rare:42 | ||||
| chr2:96637183-96637430 | Rare:42 | ||||
| chr2:96642482-96642796 | Rare:66 | ||||
| chr2:96740037-96740301 | Common:5; Rare:63 | ||||
| chr2:96857908-96858310 | Common:2; Rare:143 | ||||
| chr2:96870808-96871135 | Common:1; Rare:70 | ||||
| chr2:97094835-97094965 | Common:1; Rare:27 | ||||
| chr2:97589548-97589759 | Common:3; Rare:75 | ||||
| chr2:97590296-97590634 | Common:1; Rare:64 | ||||
| chr2:97645813-97646095 | Common:2; Rare:86 | ||||
| chr2:97664145-97664296 | Rare:34 |