| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:180606343-180606602 | Rare:80 | ||||
| chr3:180820586-180820762 | Common:3; Rare:40 | ||||
| chr3:180948439-180948719 | Common:1; Rare:61 | ||||
| chr3:182947232-182947579 | Rare:65 | ||||
| chr3:183268507-183268516 | Rare:3 | ||||
| chr3:183762570-183762641 | Rare:14 | ||||
| chr3:183833506-183833807 | Rare:87 | ||||
| chr3:183840567-183840687 | Common:1; Rare:27 | ||||
| chr3:183940209-183940461 | Rare:38 | ||||
| chr3:184090687-184090944 | Common:1; Rare:31 | ||||
| chr3:184321859-184322448 | Common:5; Rare:201; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:184322544-184323241 | Common:1; Rare:202; Clinvar:1 | ||||
| chr3:184332794-184333172 | Rare:70 | ||||
| chr3:184333305-184333541 | Rare:40 | ||||
| chr3:184348516-184348706 | Common:2; Rare:28 |