| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:193593091-193593303 | Rare:65; Clinvar:1 | ||||
| chr3:196318184-196318325 | Common:1; Rare:63 | ||||
| chr3:196568517-196568848 | Common:5; Rare:101 | ||||
| chr3:196712228-196712320 | Common:2; Rare:29 | ||||
| chr3:196942419-196942659 | Common:1; Rare:94 | ||||
| chr3:197949893-197950288 | Common:4; Rare:120; Clinvar (benign):2 | ||||
| chr4:674234-674507 | Rare:126 | ||||
| chr4:932259-932460 | Common:2; Rare:80 | ||||
| chr4:1113488-1113639 | Common:3; Rare:62 | ||||
| chr4:2468878-2469159 | Common:3; Rare:101 | ||||
| chr4:2843709-2844005 | Common:3; Rare:105 | ||||
| chr4:2934767-2935105 | Common:5; Rare:126 | ||||
| chr4:4248187-4248266 | Common:2; Rare:37 | ||||
| chr4:4290097-4290254 | Common:3; Rare:62 | ||||
| chr4:4541970-4542212 | Common:2; Rare:98 |