| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:106194243-106194543 | Common:6; Rare:127 | ||||
| chr2:106887233-106887314 | Rare:18 | ||||
| chr2:108288618-108289029 | Common:2; Rare:75 | ||||
| chr2:108449034-108449268 | Rare:94 | ||||
| chr2:108719404-108719619 | Common:2; Rare:89; Clinvar (benign):2 | ||||
| chr2:109613879-109614052 | Common:2; Rare:61 | ||||
| chr2:110678001-110678258 | Rare:86 | ||||
| chr2:111884081-111884255 | Common:1; Rare:50 | ||||
| chr2:112254999-112255198 | Common:2; Rare:83 | ||||
| chr2:112275388-112275594 | Common:1; Rare:69 | ||||
| chr2:112542119-112542493 | Common:1; Rare:116 | ||||
| chr2:112584346-112584633 | Common:1; Rare:79 | ||||
| chr2:112645701-112645944 | Common:1; Rare:89 | ||||
| chr2:112646188-112646393 | Common:2; Rare:65 | ||||
| chr2:112764577-112764861 | Common:2; Rare:94; Clinvar (pathogenic):1 |