| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200864298-200864428 | Rare:32 | ||||
| chr2:200864562-200864739 | Common:1; Rare:55 | ||||
| chr2:200889037-200889455 | Common:3; Rare:134 | ||||
| chr2:200963488-200963884 | Common:1; Rare:102 | ||||
| chr2:201071565-201072052 | Rare:111 | ||||
| chr2:201115804-201116454 | Common:2; Rare:124 | ||||
| chr2:201118574-201118825 | Rare:43 | ||||
| chr2:201122367-201122666 | Common:1; Rare:54 | ||||
| chr2:201233364-201233520 | Common:1; Rare:32 | ||||
| chr2:201451486-201451826 | Common:2; Rare:89 | ||||
| chr2:201642633-201642775 | Rare:70 | ||||
| chr2:201780884-201781179 | Common:2; Rare:91; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:202238443-202238606 | Rare:58; Clinvar:1 | ||||
| chr2:202377023-202377315 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:202635417-202635673 | Common:2; Rare:55 |