| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108719410-108719577 | Common:2; Rare:67; Clinvar (benign):2 | ||||
| chr2:109613831-109614034 | Common:2; Rare:71 | ||||
| chr2:111884124-111884257 | Rare:39 | ||||
| chr2:112254978-112255148 | Common:1; Rare:69 | ||||
| chr2:112275404-112275629 | Common:1; Rare:73 | ||||
| chr2:112584368-112584649 | Common:1; Rare:80 | ||||
| chr2:112584772-112584856 | Rare:20 | ||||
| chr2:112645707-112645959 | Common:1; Rare:95 | ||||
| chr2:112764584-112764765 | Common:1; Rare:59; Clinvar (pathogenic):1 | ||||
| chr2:113127339-113127616 | Rare:56 | ||||
| chr2:113157184-113157507 | Common:3; Rare:86 | ||||
| chr2:113198807-113198977 | Rare:64 | ||||
| chr2:113627070-113627303 | Common:3; Rare:67 | ||||
| chr2:113756483-113756734 | Common:2; Rare:74 | ||||
| chr2:113889773-113890290 | Common:8; Rare:159 |