| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:206274573-206274724 | Rare:41 | ||||
| chr2:206274816-206275064 | Common:1; Rare:78 | ||||
| chr2:206765307-206765674 | Common:3; Rare:93; Clinvar:5; Clinvar (benign):5 | ||||
| chr2:207164731-207165073 | Common:2; Rare:74 | ||||
| chr2:207165222-207165270 | Rare:11 | ||||
| chr2:207165894-207166358 | Common:2; Rare:133 | ||||
| chr2:207166360-207166452 | Common:1; Rare:49 | ||||
| chr2:207166583-207166683 | Common:1; Rare:25 | ||||
| chr2:207166726-207167063 | Common:4; Rare:126 | ||||
| chr2:207529030-207529264 | Common:1; Rare:40 | ||||
| chr2:207529266-207529313 | Common:1; Rare:10 | ||||
| chr2:207529442-207530277 | Common:3; Rare:219 | ||||
| chr2:207624265-207624358 | Rare:28 | ||||
| chr2:207624630-207624871 | Rare:64 | ||||
| chr2:207625006-207625708 | Common:2; Rare:187 |