| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:106887259-106887422 | Rare:30 | ||||
| chr2:108377753-108378000 | Common:1; Rare:44 | ||||
| chr2:108449091-108449257 | Rare:59 | ||||
| chr2:108534113-108534519 | Common:7; Rare:164 | ||||
| chr2:108621208-108621252 | Rare:3 | ||||
| chr2:108719404-108719593 | Common:2; Rare:78; Clinvar (benign):2 | ||||
| chr2:109613846-109613986 | Common:1; Rare:55 | ||||
| chr2:111884123-111884240 | Rare:36 | ||||
| chr2:112255009-112255169 | Common:1; Rare:73 | ||||
| chr2:112275392-112275629 | Common:1; Rare:81 | ||||
| chr2:112584303-112584510 | Common:2; Rare:45 | ||||
| chr2:112584536-112584633 | Rare:33 | ||||
| chr2:112584785-112584873 | Rare:21 | ||||
| chr2:112645696-112645944 | Common:1; Rare:90 | ||||
| chr2:112764575-112764859 | Common:2; Rare:96; Clinvar (pathogenic):1 |