| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:169773081-169773418 | Common:2; Rare:109 | ||||
| chr3:169812504-169812596 | Common:1; Rare:28 | ||||
| chr3:170870168-170870335 | Rare:77 | ||||
| chr3:170908580-170908845 | Common:1; Rare:74 | ||||
| chr3:172039467-172039677 | Common:1; Rare:71 | ||||
| chr3:172523371-172523581 | Common:1; Rare:53 | ||||
| chr3:177196465-177196752 | Common:2; Rare:95 | ||||
| chr3:179604622-179604877 | Common:2; Rare:98 | ||||
| chr3:180679428-180679556 | Rare:25; Clinvar:3 | ||||
| chr3:180989629-180989790 | Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:181711736-181711986 | Rare:77 | ||||
| chr3:183162680-183162896 | Common:5; Rare:47 | ||||
| chr3:184135239-184135388 | Common:2; Rare:39; Clinvar:2 | ||||
| chr3:184185890-184186210 | Common:4; Rare:117 | ||||
| chr3:184249518-184249689 | Rare:44 |