| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158732796-158732855 | Rare:10 | ||||
| chr3:158801767-158802168 | Common:4; Rare:133 | ||||
| chr3:159839794-159839965 | Rare:31 | ||||
| chr3:160399164-160399290 | Rare:29; Clinvar:2 | ||||
| chr3:160399502-160399669 | Rare:41; Clinvar:1 | ||||
| chr3:160449743-160449993 | Common:2; Rare:77 | ||||
| chr3:160565562-160565784 | Common:2; Rare:77 | ||||
| chr3:161221209-161221330 | Rare:35 | ||||
| chr3:167734832-167735198 | Common:2; Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:168095902-168096103 | Common:1; Rare:71 | ||||
| chr3:169147320-169147482 | Common:2; Rare:38 | ||||
| chr3:169772748-169772797 | Rare:10 | ||||
| chr3:169773347-169773424 | Rare:24 | ||||
| chr3:169812902-169812974 | Rare:10 | ||||
| chr3:169966632-169966858 | Common:2; Rare:89 |