| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:182793393-182793644 | Common:3; Rare:56 | ||||
| chr3:183099406-183099742 | Common:2; Rare:111; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:183253093-183253368 | Common:2; Rare:75 | ||||
| chr3:183635487-183635697 | Common:3; Rare:69 | ||||
| chr3:183884837-183884969 | Rare:53 | ||||
| chr3:184017862-184018033 | Rare:44 | ||||
| chr3:184135221-184135394 | Common:2; Rare:53; Clinvar:5 | ||||
| chr3:184155240-184155338 | Rare:28 | ||||
| chr3:184181786-184182005 | Rare:51 | ||||
| chr3:184186395-184186653 | Common:2; Rare:92 | ||||
| chr3:184248885-184249021 | Rare:68; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249516-184249771 | Common:1; Rare:81 | ||||
| chr3:184298966-184299338 | Common:4; Rare:110 | ||||
| chr3:184361582-184361770 | Rare:50 | ||||
| chr3:184711954-184712239 | Common:1; Rare:97 |