| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207165879-207166094 | Rare:42 | ||||
| chr2:207166163-207166380 | Common:3; Rare:93 | ||||
| chr2:207529553-207530119 | Common:3; Rare:145 | ||||
| chr2:207625176-207625610 | Common:1; Rare:120 | ||||
| chr2:207711582-207711886 | Rare:99 | ||||
| chr2:208025466-208025622 | Common:1; Rare:41 | ||||
| chr2:208254237-208254466 | Rare:56 | ||||
| chr2:208254937-208255235 | Common:2; Rare:72 | ||||
| chr2:208255527-208255681 | Common:2; Rare:29 | ||||
| chr2:208266032-208266056 | Common:1; Rare:12 | ||||
| chr2:208266111-208266391 | Common:6; Rare:93; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:209423756-209424113 | Common:1; Rare:105 | ||||
| chr2:210002369-210002663 | Common:6; Rare:95 | ||||
| chr2:210170686-210170897 | Common:1; Rare:82 | ||||
| chr2:210225368-210225610 | Rare:47 |