| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:95165644-95165828 | Rare:58 | ||||
| chr2:95207431-95207604 | Rare:65 | ||||
| chr2:95402594-95402757 | Rare:56 | ||||
| chr2:96145438-96145610 | Common:2; Rare:41 | ||||
| chr2:96208208-96208427 | Rare:114 | ||||
| chr2:96208787-96208954 | Common:3; Rare:67 | ||||
| chr2:96265959-96266443 | Common:2; Rare:139; Clinvar:1 | ||||
| chr2:96305414-96305666 | Common:2; Rare:97; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:96638292-96638660 | Common:1; Rare:87 | ||||
| chr2:96869897-96870145 | Common:2; Rare:51 | ||||
| chr2:97094820-97094966 | Common:1; Rare:30 | ||||
| chr2:97645840-97646108 | Common:3; Rare:84 | ||||
| chr2:97663902-97664272 | Common:1; Rare:114 | ||||
| chr2:98608409-98608637 | Common:1; Rare:100; Clinvar (benign):1 | ||||
| chr2:98869253-98869350 | Common:1; Rare:21 |