| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207335286-207335372 | Common:2; Rare:14 | ||||
| chr2:207530731-207530980 | Rare:65 | ||||
| chr2:207626515-207626537 | Rare:2 | ||||
| chr2:207627219-207627343 | Common:1; Rare:38 | ||||
| chr2:207792195-207792444 | Common:2; Rare:39 | ||||
| chr2:209831529-209831558 | Rare:7; Clinvar (pathogenic):1 | ||||
| chr2:209943334-209943653 | Common:1; Rare:70 | ||||
| chr2:210162551-210162675 | Common:1; Rare:23 | ||||
| chr2:210169953-210170050 | Common:1; Rare:20 | ||||
| chr2:211034029-211034074 | Rare:8 | ||||
| chr2:211258788-211259106 | Common:20; Rare:82 | ||||
| chr2:211259935-211260366 | Common:5; Rare:105 | ||||
| chr2:211349064-211349266 | Common:1; Rare:32 | ||||
| chr2:211453690-211453732 | Rare:10 | ||||
| chr2:211454880-211454905 | Common:1; Rare:3 |