| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46521210-46521524 | Common:6; Rare:54 | ||||
| chr2:46846164-46846473 | Common:1; Rare:66 | ||||
| chr2:46940412-46940633 | Common:3; Rare:46 | ||||
| chr2:47803303-47803450 | Common:1; Rare:56; Clinvar:7; Clinvar (benign):12 | ||||
| chr2:47906415-47906818 | Common:2; Rare:155 | ||||
| chr2:48111574-48111808 | Rare:60 | ||||
| chr2:48315627-48315776 | Rare:48 | ||||
| chr2:48510425-48510680 | Common:3; Rare:50 | ||||
| chr2:53739022-53739341 | Common:1; Rare:57 | ||||
| chr2:53797349-53797569 | Common:1; Rare:49 | ||||
| chr2:54658907-54659271 | Common:1; Rare:94 | ||||
| chr2:54667488-54667646 | Common:1; Rare:48 | ||||
| chr2:55100281-55100522 | Common:1; Rare:39 | ||||
| chr2:55282048-55282356 | Common:7; Rare:92 | ||||
| chr2:55870719-55871122 | Common:1; Rare:87; Clinvar (benign):1 |