| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:95165651-95165817 | Rare:49 | ||||
| chr2:96265987-96266287 | Common:2; Rare:87 | ||||
| chr2:96305475-96305618 | Common:2; Rare:49; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:96335710-96335801 | Common:1; Rare:31 | ||||
| chr2:97645870-97646089 | Common:2; Rare:65 | ||||
| chr2:98608431-98608649 | Common:1; Rare:98 | ||||
| chr2:99180986-99181213 | Common:2; Rare:68 | ||||
| chr2:101002156-101002304 | Rare:55 | ||||
| chr2:105337475-105337620 | Common:1; Rare:66 | ||||
| chr2:105398993-105399258 | Common:1; Rare:92 | ||||
| chr2:108449081-108449242 | Rare:59 | ||||
| chr2:108534203-108534481 | Common:7; Rare:114 | ||||
| chr2:111884171-111884255 | Rare:18 | ||||
| chr2:112584410-112584633 | Common:1; Rare:61 | ||||
| chr2:112645707-112645944 | Common:1; Rare:87 |