| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:205682110-205682532 | Rare:156 | ||||
| chr2:206085697-206086711 | Common:9; Rare:407 | ||||
| chr2:206159273-206159995 | Common:12; Rare:546; Clinvar (benign):4 | ||||
| chr2:206159950-206160450 | Common:2; Rare:152 | ||||
| chr2:206274834-206275105 | Common:2; Rare:199 | ||||
| chr2:206443350-206443710 | Common:1; Rare:133 | ||||
| chr2:206765268-206765691 | Common:9; Rare:339; Clinvar:14; Clinvar (benign):17 | ||||
| chr2:207165045-207165650 | Common:5; Rare:239 | ||||
| chr2:207165879-207166472 | Common:11; Rare:540 | ||||
| chr2:207166470-207166740 | Common:6; Rare:127 | ||||
| chr2:207166748-207167141 | Common:10; Rare:322 | ||||
| chr2:207167047-207167430 | Common:5; Rare:152 | ||||
| chr2:207529461-207530352 | Common:9; Rare:504 | ||||
| chr2:207624434-207624834 | Rare:185 | ||||
| chr2:207625152-207625597 | Common:4; Rare:303 |