| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160420478-160420770 | Rare:68 | ||||
| chr3:160449706-160450022 | Common:2; Rare:105 | ||||
| chr3:160565284-160565845 | Common:3; Rare:190 | ||||
| chr3:161105039-161105399 | Common:4; Rare:109 | ||||
| chr3:161221127-161221407 | Common:2; Rare:82 | ||||
| chr3:161221426-161221630 | Common:2; Rare:46 | ||||
| chr3:167734818-167735205 | Common:3; Rare:122; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735563-167735743 | Rare:43 | ||||
| chr3:168094769-168094938 | Common:1; Rare:32 | ||||
| chr3:168095109-168095238 | Rare:43 | ||||
| chr3:168095827-168096207 | Common:2; Rare:124 | ||||
| chr3:169146475-169146622 | Common:1; Rare:61 | ||||
| chr3:169769549-169769712 | Common:1; Rare:62 | ||||
| chr3:169772707-169772846 | Common:1; Rare:35 | ||||
| chr3:169773287-169773456 | Common:1; Rare:63 |