| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:38990749-38990982 | Common:1; Rare:35 | ||||
| chr2:39042029-39042252 | Rare:49 | ||||
| chr2:39093030-39093321 | Rare:60 | ||||
| chr2:42315912-42316014 | Common:1; Rare:32 | ||||
| chr2:42810453-42810544 | Common:1; Rare:46 | ||||
| chr2:43006230-43006294 | Rare:14 | ||||
| chr2:43194994-43195113 | Rare:20 | ||||
| chr2:43218800-43218977 | Rare:37 | ||||
| chr2:43219143-43219343 | Common:1; Rare:47 | ||||
| chr2:43227611-43227830 | Rare:80 | ||||
| chr2:46308867-46309130 | Common:4; Rare:53 | ||||
| chr2:46322517-46322657 | Rare:20 | ||||
| chr2:46333011-46333292 | Rare:63 | ||||
| chr2:46382174-46382520 | Common:4; Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:47173172-47173494 | Common:3; Rare:66 |