| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218959462-218959679 | Rare:63 | ||||
| chr2:219160212-219160402 | Common:1; Rare:37 | ||||
| chr2:219160475-219160702 | Common:5; Rare:62 | ||||
| chr2:219160743-219160966 | Common:1; Rare:58 | ||||
| chr2:219176252-219176473 | Common:2; Rare:72 | ||||
| chr2:219176834-219177295 | Common:5; Rare:125 | ||||
| chr2:219177804-219178004 | Common:7; Rare:41 | ||||
| chr2:219178026-219178323 | Common:8; Rare:133 | ||||
| chr2:219178537-219178847 | Common:1; Rare:79 | ||||
| chr2:219206387-219206493 | Rare:23 | ||||
| chr2:219206549-219207085 | Common:1; Rare:198 | ||||
| chr2:219217885-219218080 | Common:1; Rare:27 | ||||
| chr2:219218424-219218570 | Common:1; Rare:61; Clinvar (pathogenic):1 | ||||
| chr2:219218866-219219171 | Common:2; Rare:100 | ||||
| chr2:219228473-219228602 | Common:1; Rare:29 |