| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27663345-27663983 | Common:1; Rare:413 | ||||
| chr2:27771509-27771813 | Common:2; Rare:174 | ||||
| chr2:27890341-27890834 | Common:2; Rare:266 | ||||
| chr2:28392622-28392996 | Rare:252 | ||||
| chr2:28751497-28752145 | Common:8; Rare:510 | ||||
| chr2:28870218-28870483 | Rare:199 | ||||
| chr2:28894354-28894829 | Common:5; Rare:288 | ||||
| chr2:28895300-28895620 | Common:6; Rare:140 | ||||
| chr2:30146551-30147127 | Common:10; Rare:329 | ||||
| chr2:30447176-30447331 | Rare:87 | ||||
| chr2:32010448-32010825 | Common:1; Rare:91 | ||||
| chr2:32010907-32011125 | Rare:118 | ||||
| chr2:32039732-32039889 | Rare:89 | ||||
| chr2:32063350-32063762 | Common:2; Rare:282; Clinvar:2 | ||||
| chr2:32063775-32064020 | Common:2; Rare:188; Clinvar:9; Clinvar (benign):5; Clinvar (pathogenic):2 |