| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:25878455-25878770 | Common:4; Rare:99 | ||||
| chr2:26033764-26034142 | Common:4; Rare:139 | ||||
| chr2:26194619-26194897 | Common:1; Rare:46; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:26244564-26244977 | Common:2; Rare:154; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345798-26346176 | Common:1; Rare:112 | ||||
| chr2:27032841-27033011 | Rare:69 | ||||
| chr2:27051536-27051673 | Rare:38 | ||||
| chr2:27071503-27071870 | Common:1; Rare:109 | ||||
| chr2:27078968-27079005 | Rare:8 | ||||
| chr2:27086553-27086792 | Common:1; Rare:68; Clinvar (benign):1 | ||||
| chr2:27211910-27212065 | Common:3; Rare:62 | ||||
| chr2:27212232-27212370 | Common:1; Rare:72 | ||||
| chr2:27323043-27323150 | Rare:27; Clinvar (benign):1 | ||||
| chr2:27356750-27357170 | Common:2; Rare:121 | ||||
| chr2:27370277-27370641 | Common:1; Rare:150 |