| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97664194-97664413 | Rare:43 | ||||
| chr2:97664423-97664613 | Rare:42 | ||||
| chr2:97995135-97995327 | Common:2; Rare:50 | ||||
| chr2:97995390-97995524 | Common:2; Rare:41 | ||||
| chr2:97995581-97995715 | Rare:40 | ||||
| chr2:97995764-97996033 | Common:3; Rare:94 | ||||
| chr2:97996110-97996495 | Common:2; Rare:123 | ||||
| chr2:98086571-98086624 | Rare:6 | ||||
| chr2:98086990-98087250 | Common:1; Rare:69 | ||||
| chr2:98444666-98444992 | Common:1; Rare:122 | ||||
| chr2:98608161-98608283 | Common:1; Rare:29 | ||||
| chr2:98608306-98608674 | Common:1; Rare:149; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:98608772-98608878 | Rare:29 | ||||
| chr2:98609089-98609280 | Common:1; Rare:38 | ||||
| chr2:98730224-98730407 | Rare:34 |