| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3558251-3558471 | Common:5; Rare:97 | ||||
| chr2:3575107-3575325 | Common:1; Rare:62; Clinvar (benign):4 | ||||
| chr2:9423505-9423693 | Rare:59 | ||||
| chr2:10302722-10302993 | Common:5; Rare:81 | ||||
| chr2:10448294-10448689 | Common:1; Rare:120 | ||||
| chr2:10689956-10689994 | Common:1; Rare:8 | ||||
| chr2:20051552-20051807 | Common:1; Rare:63 | ||||
| chr2:24076241-24076551 | Rare:83 | ||||
| chr2:24971939-24972145 | Common:1; Rare:58 | ||||
| chr2:26244579-26244966 | Common:2; Rare:141; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:27078751-27079017 | Common:2; Rare:62 | ||||
| chr2:27212266-27212372 | Common:1; Rare:52 | ||||
| chr2:27356761-27356853 | Rare:22 | ||||
| chr2:27370297-27370654 | Common:1; Rare:145 | ||||
| chr2:27582985-27583106 | Rare:44 |