| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:88055732-88055939 | Rare:77 | ||||
| chr2:88691456-88691897 | Common:2; Rare:165; Clinvar:1 | ||||
| chr2:95121736-95122084 | Common:1; Rare:121 | ||||
| chr2:95165644-95165852 | Rare:69 | ||||
| chr2:95207425-95207572 | Rare:59 | ||||
| chr2:95402615-95402757 | Rare:48 | ||||
| chr2:95991798-95991993 | Common:1; Rare:38 | ||||
| chr2:96208252-96208427 | Rare:86 | ||||
| chr2:96208805-96208979 | Common:3; Rare:67 | ||||
| chr2:96265959-96266340 | Common:2; Rare:115; Clinvar:1 | ||||
| chr2:96305475-96305662 | Common:2; Rare:71; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:96325258-96325376 | Rare:31 | ||||
| chr2:96335707-96335812 | Common:1; Rare:34 | ||||
| chr2:96740045-96740294 | Common:5; Rare:57 | ||||
| chr2:96857914-96858258 | Common:2; Rare:127 |