| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:46553058-46553405 | Common:4; Rare:101 | ||||
| chr13:48001203-48001408 | Common:1; Rare:94; Clinvar:4; Clinvar (benign):8 | ||||
| chr13:48037673-48037820 | Common:2; Rare:75; Clinvar:2 | ||||
| chr13:48037908-48038096 | Common:5; Rare:63 | ||||
| chr13:48233053-48233475 | Common:3; Rare:146 | ||||
| chr13:48303674-48304047 | Common:1; Rare:122; Clinvar:15; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr13:48492611-48493026 | Common:3; Rare:81 | ||||
| chr13:48533038-48533110 | Common:2; Rare:23 | ||||
| chr13:48533163-48533351 | Rare:51 | ||||
| chr13:48975619-48975961 | Common:2; Rare:105 | ||||
| chr13:48976135-48976281 | Rare:37 | ||||
| chr13:48976531-48976870 | Common:1; Rare:99 | ||||
| chr13:49247798-49247994 | Rare:56 | ||||
| chr13:49401260-49401658 | Common:2; Rare:78 | ||||
| chr13:49443961-49444501 | Common:1; Rare:166 |