| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:25878453-25878648 | Common:1; Rare:61 | ||||
| chr2:25982411-25982612 | Common:1; Rare:52 | ||||
| chr2:26033790-26034159 | Common:3; Rare:132 | ||||
| chr2:26034294-26034495 | Common:1; Rare:49 | ||||
| chr2:26194568-26194836 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr2:26195108-26195325 | Rare:79; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr2:26244592-26244965 | Common:2; Rare:135; Clinvar:5; Clinvar (benign):8 | ||||
| chr2:26345785-26346156 | Common:1; Rare:112 | ||||
| chr2:26764203-26764325 | Common:1; Rare:47 | ||||
| chr2:27032862-27033009 | Rare:57 | ||||
| chr2:27051546-27051743 | Rare:63 | ||||
| chr2:27071525-27071898 | Common:1; Rare:113 | ||||
| chr2:27086601-27086792 | Common:1; Rare:54; Clinvar (benign):1 | ||||
| chr2:27211910-27212103 | Common:3; Rare:73 | ||||
| chr2:27212242-27212383 | Common:2; Rare:72 |