| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203014543-203014629 | Rare:30 | ||||
| chr2:203014680-203014955 | Common:1; Rare:82 | ||||
| chr2:203238640-203239068 | Common:3; Rare:129 | ||||
| chr2:203239259-203239331 | Rare:25 | ||||
| chr2:203328122-203328564 | Common:2; Rare:147 | ||||
| chr2:203328694-203328924 | Rare:61 | ||||
| chr2:205682222-205682563 | Rare:73 | ||||
| chr2:206085765-206085965 | Common:1; Rare:57 | ||||
| chr2:206086085-206086255 | Rare:24 | ||||
| chr2:206086281-206086303 | Rare:3 | ||||
| chr2:206159178-206159989 | Common:6; Rare:226; Clinvar (benign):2 | ||||
| chr2:206765269-206765654 | Common:3; Rare:111; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165892-207166088 | Rare:37 | ||||
| chr2:207529748-207530120 | Common:3; Rare:105 | ||||
| chr2:207625226-207625483 | Common:1; Rare:71 |