| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26401811-26401978 | Common:4; Rare:50 | ||||
| chr2:26764183-26764357 | Common:2; Rare:68 | ||||
| chr2:27032822-27033011 | Rare:76 | ||||
| chr2:27051542-27051708 | Rare:49 | ||||
| chr2:27086601-27086792 | Common:1; Rare:54; Clinvar (benign):1 | ||||
| chr2:27118886-27119189 | Common:1; Rare:74 | ||||
| chr2:27134615-27134729 | Rare:47 | ||||
| chr2:27211417-27211427 | Rare:1 | ||||
| chr2:27211742-27212103 | Common:3; Rare:123 | ||||
| chr2:27212215-27212455 | Common:2; Rare:124 | ||||
| chr2:27217296-27217544 | Rare:107 | ||||
| chr2:27323009-27323161 | Rare:45; Clinvar (benign):1 | ||||
| chr2:27356177-27356286 | Rare:26 | ||||
| chr2:27356738-27356913 | Rare:42 | ||||
| chr2:27356961-27357199 | Common:2; Rare:87 |