| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:8679119-8679245 | Rare:51 | ||||
| chr2:8683189-8683399 | Common:2; Rare:60 | ||||
| chr2:9423012-9423697 | Common:2; Rare:172 | ||||
| chr2:9474505-9474642 | Common:6; Rare:68 | ||||
| chr2:9555550-9555966 | Common:2; Rare:142; Clinvar:2 | ||||
| chr2:9630320-9630766 | Common:6; Rare:191 | ||||
| chr2:9630945-9631268 | Common:2; Rare:101 | ||||
| chr2:9843392-9843544 | Common:5; Rare:43 | ||||
| chr2:10043382-10043658 | Common:4; Rare:118; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:10302722-10302921 | Common:3; Rare:69 | ||||
| chr2:10448381-10448689 | Common:1; Rare:92 | ||||
| chr2:10689847-10690089 | Common:4; Rare:93 | ||||
| chr2:10812683-10812967 | Common:3; Rare:112 | ||||
| chr2:11344137-11344191 | Rare:11 | ||||
| chr2:11344942-11345123 | Common:3; Rare:58 |