| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:25252228-25252502 | Rare:59 | ||||
| chr2:25878460-25878772 | Common:4; Rare:98 | ||||
| chr2:26033767-26034142 | Common:4; Rare:137 | ||||
| chr2:26244581-26244943 | Common:2; Rare:132; Clinvar:5; Clinvar (benign):8 | ||||
| chr2:26345766-26346165 | Common:1; Rare:122 | ||||
| chr2:26764230-26764305 | Rare:25 | ||||
| chr2:26785748-26786032 | Rare:72 | ||||
| chr2:27071595-27071872 | Common:1; Rare:84 | ||||
| chr2:27211794-27212095 | Common:3; Rare:100 | ||||
| chr2:27212261-27212366 | Common:1; Rare:54 | ||||
| chr2:27217220-27217421 | Rare:76 | ||||
| chr2:27323029-27323160 | Rare:37; Clinvar (benign):1 | ||||
| chr2:27356743-27356854 | Rare:28 | ||||
| chr2:27356977-27357193 | Common:2; Rare:79 | ||||
| chr2:27370310-27370636 | Common:1; Rare:129 |