| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:20447239-20447566 | Common:2; Rare:109 | ||||
| chr2:20651038-20651307 | Common:1; Rare:82 | ||||
| chr2:21043862-21043935 | Common:2; Rare:30; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:21043941-21044186 | Common:1; Rare:59; Clinvar:2 | ||||
| chr2:23926693-23926790 | Rare:34 | ||||
| chr2:23926808-23926854 | Rare:15 | ||||
| chr2:23927057-23927330 | Common:3; Rare:95 | ||||
| chr2:23940379-23940529 | Common:3; Rare:56 | ||||
| chr2:24076290-24076951 | Common:3; Rare:124 | ||||
| chr2:24084243-24084509 | Common:6; Rare:110 | ||||
| chr2:24084512-24084579 | Rare:14 | ||||
| chr2:24360394-24360675 | Common:3; Rare:94 | ||||
| chr2:24793089-24793182 | Rare:48 | ||||
| chr2:24971684-24971836 | Common:1; Rare:56 | ||||
| chr2:24971907-24972136 | Common:1; Rare:75 |