| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:69052219-69052397 | Common:3; Rare:74 | ||||
| chr3:69080346-69080460 | Rare:47 | ||||
| chr3:69084895-69085084 | Common:2; Rare:56 | ||||
| chr3:69739249-69739505 | Rare:84 | ||||
| chr3:71581918-71582180 | Common:1; Rare:64 | ||||
| chr3:71583595-71583728 | Rare:50 | ||||
| chr3:71725222-71725514 | Common:2; Rare:106 | ||||
| chr3:72848336-72848480 | Common:1; Rare:60 | ||||
| chr3:73624174-73624346 | Rare:46 | ||||
| chr3:73624924-73625065 | Common:3; Rare:44 | ||||
| chr3:81761510-81761755 | Common:8; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:88058903-88059461 | Common:3; Rare:206 | ||||
| chr3:88149605-88150003 | Common:1; Rare:101 | ||||
| chr3:93979918-93980204 | Common:4; Rare:104; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:94062884-94063101 | Rare:53 |