| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:32031571-32031605 | Rare:7 | ||||
| chr13:32031607-32031798 | Common:1; Rare:57 | ||||
| chr13:32315426-32315571 | Rare:44; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:32315848-32316082 | Common:2; Rare:50; Clinvar (benign):3 | ||||
| chr13:32538626-32538955 | Common:1; Rare:93 | ||||
| chr13:32586220-32586593 | Common:2; Rare:114 | ||||
| chr13:33016035-33016079 | Common:1; Rare:12 | ||||
| chr13:33285626-33285861 | Common:1; Rare:56 | ||||
| chr13:34942164-34942294 | Common:3; Rare:39 | ||||
| chr13:36345546-36345620 | Common:1; Rare:16 | ||||
| chr13:36346252-36346477 | Common:3; Rare:62; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:36999275-36999451 | Rare:71 | ||||
| chr13:37000550-37000815 | Common:2; Rare:87; Clinvar (pathogenic):1 | ||||
| chr13:37059585-37059765 | Common:1; Rare:61 | ||||
| chr13:38349543-38349920 | Common:4; Rare:129; Clinvar (pathogenic):1 |