| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:206086030-206086247 | Rare:49 | ||||
| chr2:206086220-206086700 | Common:2; Rare:134 | ||||
| chr2:206159343-206160003 | Common:8; Rare:381; Clinvar (benign):2 | ||||
| chr2:206274917-206275057 | Common:1; Rare:49 | ||||
| chr2:206765275-206765689 | Common:6; Rare:220; Clinvar:9; Clinvar (benign):11 | ||||
| chr2:207165880-207166480 | Common:7; Rare:287 | ||||
| chr2:207529739-207530117 | Common:5; Rare:184 | ||||
| chr2:207624357-207624693 | Common:5; Rare:158 | ||||
| chr2:207625183-207625613 | Common:2; Rare:230 | ||||
| chr2:207625830-207626190 | Common:5; Rare:125 | ||||
| chr2:207710950-207711230 | Common:2; Rare:65 | ||||
| chr2:207711300-207711665 | Common:2; Rare:203 | ||||
| chr2:207769530-207769809 | Common:1; Rare:127 | ||||
| chr2:207769818-207770200 | Common:2; Rare:227 | ||||
| chr2:208025419-208025645 | Common:4; Rare:99 |