| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:19901652-19901711 | Rare:29 | ||||
| chr2:19990087-19990220 | Rare:33 | ||||
| chr2:20446877-20447095 | Common:2; Rare:83 | ||||
| chr2:20651053-20651200 | Rare:42 | ||||
| chr2:20823056-20823145 | Rare:37 | ||||
| chr2:23927058-23927325 | Common:3; Rare:92 | ||||
| chr2:24076297-24076887 | Common:2; Rare:118 | ||||
| chr2:24123272-24123506 | Common:1; Rare:62 | ||||
| chr2:24793041-24793154 | Rare:50 | ||||
| chr2:24971889-24972136 | Common:1; Rare:79 | ||||
| chr2:26244528-26245118 | Common:2; Rare:196; Clinvar:7; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:26345802-26346165 | Common:1; Rare:109 | ||||
| chr2:26764185-26764337 | Common:1; Rare:63 | ||||
| chr2:27211920-27212072 | Common:3; Rare:60 | ||||
| chr2:27212225-27212383 | Common:2; Rare:84 |