| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158732159-158732383 | Common:8; Rare:69 | ||||
| chr3:158732726-158732848 | Common:1; Rare:22 | ||||
| chr3:158801993-158802164 | Common:2; Rare:78 | ||||
| chr3:160399177-160399307 | Rare:35; Clinvar:2 | ||||
| chr3:160399518-160399669 | Rare:31 | ||||
| chr3:160449737-160449926 | Common:1; Rare:62 | ||||
| chr3:160565292-160565525 | Common:1; Rare:69 | ||||
| chr3:160565569-160565784 | Common:1; Rare:74 | ||||
| chr3:161105277-161105563 | Common:3; Rare:77 | ||||
| chr3:161221209-161221390 | Common:2; Rare:57 | ||||
| chr3:167734807-167735180 | Common:2; Rare:122; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:169147291-169147397 | Common:1; Rare:25 | ||||
| chr3:169769599-169769727 | Common:2; Rare:44 | ||||
| chr3:169772748-169772825 | Rare:18 | ||||
| chr3:169773331-169773415 | Rare:25 |