| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:147844088-147844371 | Common:3; Rare:78 | ||||
| chr2:147844384-147844751 | Common:7; Rare:126 | ||||
| chr2:147844765-147844833 | Rare:17 | ||||
| chr2:147845287-147845412 | Common:1; Rare:24 | ||||
| chr2:148020652-148021138 | Common:2; Rare:115; Clinvar (benign):2 | ||||
| chr2:148021539-148021665 | Rare:24 | ||||
| chr2:148644611-148644846 | Rare:78 | ||||
| chr2:148644965-148645032 | Rare:21 | ||||
| chr2:148645108-148645450 | Rare:133 | ||||
| chr2:148645711-148645785 | Rare:26 | ||||
| chr2:148874997-148875257 | Common:3; Rare:51 | ||||
| chr2:149037962-149038133 | Common:1; Rare:24 | ||||
| chr2:149038495-149038817 | Common:3; Rare:92 | ||||
| chr2:149038857-149038901 | Common:1; Rare:13 | ||||
| chr2:149329873-149330070 | Common:1; Rare:47 |