| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30306987-30307197 | Common:5; Rare:49 | ||||
| chr13:30307404-30307615 | Common:2; Rare:69 | ||||
| chr13:30465795-30466148 | Common:1; Rare:117 | ||||
| chr13:30617556-30618010 | Common:1; Rare:146 | ||||
| chr13:30735371-30735633 | Common:2; Rare:56 | ||||
| chr13:32315426-32315576 | Rare:44; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:32428116-32428194 | Rare:14 | ||||
| chr13:32538684-32539049 | Common:1; Rare:98 | ||||
| chr13:32586225-32586582 | Common:2; Rare:108 | ||||
| chr13:33818011-33818217 | Common:1; Rare:93 | ||||
| chr13:36999281-36999465 | Rare:73 | ||||
| chr13:37000259-37000389 | Common:2; Rare:23 | ||||
| chr13:37000550-37000815 | Common:2; Rare:87; Clinvar (pathogenic):1 | ||||
| chr13:37059584-37059758 | Common:1; Rare:57 | ||||
| chr13:39603125-39603306 | Common:1; Rare:62 |