| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:106194237-106194568 | Common:6; Rare:140 | ||||
| chr2:108534148-108534477 | Common:7; Rare:132 | ||||
| chr2:108719372-108719625 | Common:3; Rare:104; Clinvar (benign):2 | ||||
| chr2:110677993-110678244 | Rare:86 | ||||
| chr2:110732407-110732641 | Rare:80 | ||||
| chr2:111884037-111884214 | Common:1; Rare:46 | ||||
| chr2:111898282-111898618 | Common:2; Rare:78 | ||||
| chr2:112255019-112255182 | Common:2; Rare:75 | ||||
| chr2:112275404-112275634 | Common:1; Rare:74 | ||||
| chr2:112584296-112584633 | Common:2; Rare:90 | ||||
| chr2:112645713-112645959 | Common:1; Rare:92 | ||||
| chr2:113437567-113437892 | Common:4; Rare:111 | ||||
| chr2:113627082-113627302 | Common:2; Rare:63 | ||||
| chr2:113756582-113756806 | Common:3; Rare:85 | ||||
| chr2:113889773-113890165 | Common:7; Rare:124 |