| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61470658-61471032 | Common:1; Rare:122 | ||||
| chr2:61471126-61471386 | Common:2; Rare:99 | ||||
| chr2:61492035-61492732 | Common:2; Rare:111; Clinvar (pathogenic):1 | ||||
| chr2:61502020-61502262 | Common:3; Rare:75 | ||||
| chr2:61536589-61536761 | Common:1; Rare:52 | ||||
| chr2:61537207-61537296 | Rare:21 | ||||
| chr2:61537568-61537845 | Common:2; Rare:79 | ||||
| chr2:61537973-61538390 | Common:3; Rare:96 | ||||
| chr2:61853973-61854244 | Common:3; Rare:108; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61887875-61887959 | Rare:19 | ||||
| chr2:61888373-61888739 | Common:1; Rare:163 | ||||
| chr2:61905716-61905848 | Rare:37 | ||||
| chr2:62195977-62196134 | Common:1; Rare:49 | ||||
| chr2:62506148-62506293 | Common:1; Rare:58 | ||||
| chr2:62706705-62707062 | Rare:66 |