| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108449067-108449277 | Rare:88 | ||||
| chr2:108468738-108468993 | Common:2; Rare:64 | ||||
| chr2:108469370-108469731 | Rare:87 | ||||
| chr2:108482146-108482426 | Rare:59 | ||||
| chr2:108534186-108534502 | Common:7; Rare:127 | ||||
| chr2:108719404-108719635 | Common:2; Rare:95; Clinvar (benign):2 | ||||
| chr2:109613808-109614013 | Common:2; Rare:71 | ||||
| chr2:110204935-110205067 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:111122425-111122771 | Common:3; Rare:142 | ||||
| chr2:111884117-111884257 | Rare:41 | ||||
| chr2:111898282-111898686 | Common:2; Rare:91 | ||||
| chr2:111898806-111899063 | Common:1; Rare:63; Clinvar (benign):1 | ||||
| chr2:112055157-112055347 | Common:5; Rare:62 | ||||
| chr2:112055455-112055572 | Common:1; Rare:29 | ||||
| chr2:112055578-112055612 | Common:1; Rare:10 |