| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:167734807-167735084 | Common:2; Rare:95; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735617-167735746 | Rare:32 | ||||
| chr3:168095882-168096228 | Common:1; Rare:115 | ||||
| chr3:169772748-169772831 | Rare:20 | ||||
| chr3:169773336-169773424 | Rare:25 | ||||
| chr3:169812886-169813077 | Common:2; Rare:34 | ||||
| chr3:169966706-169966843 | Rare:58 | ||||
| chr3:170222394-170222545 | Common:1; Rare:52 | ||||
| chr3:170870131-170870359 | Rare:108 | ||||
| chr3:170908552-170908845 | Common:1; Rare:84 | ||||
| chr3:171460469-171460613 | Rare:39 | ||||
| chr3:171460790-171460959 | Rare:40 | ||||
| chr3:171666308-171666451 | Common:2; Rare:39 | ||||
| chr3:171771230-171771513 | Common:2; Rare:57 | ||||
| chr3:171809774-171809814 | Rare:8 |