| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:99180985-99181231 | Common:2; Rare:71 | ||||
| chr2:99337203-99337425 | Rare:72 | ||||
| chr2:101002142-101002318 | Rare:69 | ||||
| chr2:102736846-102736951 | Common:1; Rare:46 | ||||
| chr2:105037845-105038104 | Common:3; Rare:90 | ||||
| chr2:105337496-105337593 | Rare:43 | ||||
| chr2:105398986-105399204 | Rare:77 | ||||
| chr2:108449047-108449271 | Rare:90 | ||||
| chr2:108534204-108534528 | Common:7; Rare:133 | ||||
| chr2:108719383-108719546 | Common:2; Rare:64 | ||||
| chr2:111884121-111884240 | Rare:36 | ||||
| chr2:112255012-112255152 | Common:1; Rare:64 | ||||
| chr2:112584410-112584633 | Common:1; Rare:61 | ||||
| chr2:112645715-112645944 | Common:1; Rare:84 | ||||
| chr2:112764575-112764843 | Common:2; Rare:87; Clinvar (pathogenic):1 |