| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:185586004-185586380 | Common:1; Rare:91 | ||||
| chr3:185937911-185938188 | Common:2; Rare:131 | ||||
| chr3:186567274-186567491 | Common:3; Rare:61 | ||||
| chr3:186783202-186783617 | Common:2; Rare:174 | ||||
| chr3:186806402-186806567 | Rare:54 | ||||
| chr3:190120374-190120512 | Rare:58; Clinvar (pathogenic):1 | ||||
| chr3:192917840-192918016 | Common:2; Rare:80 | ||||
| chr3:193240551-193240773 | Common:2; Rare:43 | ||||
| chr3:193240975-193241392 | Common:4; Rare:137 | ||||
| chr3:193593090-193593356 | Rare:84; Clinvar:1 | ||||
| chr3:195892734-195892905 | Common:2; Rare:26 | ||||
| chr3:196287650-196287820 | Common:1; Rare:53 | ||||
| chr3:196318184-196318326 | Common:1; Rare:63 | ||||
| chr3:196432395-196432550 | Common:1; Rare:68 | ||||
| chr3:196503665-196503952 | Common:5; Rare:100 |