| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42936309-42936402 | Common:1; Rare:29 | ||||
| chr3:43621907-43622322 | Common:2; Rare:121; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690817-43690995 | Common:3; Rare:96; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:43691556-43691663 | Common:1; Rare:17 | ||||
| chr3:44338059-44338190 | Common:2; Rare:46 | ||||
| chr3:44338675-44338798 | Common:3; Rare:46 | ||||
| chr3:44477646-44477694 | Rare:11 | ||||
| chr3:44761575-44761695 | Common:3; Rare:61 | ||||
| chr3:44861767-44861919 | Common:2; Rare:68 | ||||
| chr3:44976080-44976280 | Common:2; Rare:80 | ||||
| chr3:45689180-45689464 | Common:1; Rare:96 | ||||
| chr3:45995765-45995904 | Rare:29; Clinvar:1 | ||||
| chr3:46407054-46407275 | Rare:40 | ||||
| chr3:46693642-46693774 | Common:1; Rare:36 | ||||
| chr3:46812559-46812694 | Rare:38 |