| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108719373-108719750 | Common:4; Rare:161; Clinvar (benign):3 | ||||
| chr2:109613833-109614038 | Common:2; Rare:73 | ||||
| chr2:110115627-110115886 | Common:2; Rare:74 | ||||
| chr2:110245491-110245736 | |||||
| chr2:111122427-111122699 | Common:2; Rare:113 | ||||
| chr2:111884164-111884453 | Common:3; Rare:85 | ||||
| chr2:111898260-111898656 | Common:2; Rare:100 | ||||
| chr2:112055126-112055299 | Common:3; Rare:43 | ||||
| chr2:112055430-112055615 | Common:3; Rare:50 | ||||
| chr2:112275384-112275637 | Common:1; Rare:89 | ||||
| chr2:112542320-112542483 | Common:1; Rare:69 | ||||
| chr2:112584410-112584633 | Common:1; Rare:61 | ||||
| chr2:112645661-112645954 | Common:2; Rare:105 | ||||
| chr2:113198816-113198994 | Rare:62 | ||||
| chr2:113236871-113236989 | Common:2; Rare:19 |