| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:34941981-34942306 | Common:3; Rare:84 | ||||
| chr13:36214533-36214609 | Rare:34 | ||||
| chr13:36297712-36297968 | Common:1; Rare:95 | ||||
| chr13:36314084-36314156 | Common:1; Rare:13 | ||||
| chr13:36345551-36345663 | Common:1; Rare:20 | ||||
| chr13:36346233-36346531 | Common:3; Rare:80; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:36346613-36346787 | Common:4; Rare:49 | ||||
| chr13:36431448-36431971 | Common:1; Rare:133 | ||||
| chr13:36819092-36819139 | Rare:19 | ||||
| chr13:36920132-36920378 | Common:6; Rare:113; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:36999265-36999467 | Rare:82 | ||||
| chr13:37000023-37000403 | Common:2; Rare:90 | ||||
| chr13:37000736-37000815 | Rare:33; Clinvar (pathogenic):1 | ||||
| chr13:37059430-37059758 | Common:1; Rare:96 | ||||
| chr13:37105504-37105613 | Common:2; Rare:34 |