| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:20525801-20525929 | Common:1; Rare:55 | ||||
| chr13:20567044-20567229 | Common:1; Rare:64 | ||||
| chr13:20773929-20773997 | Rare:20 | ||||
| chr13:21140378-21140624 | Rare:110 | ||||
| chr13:21176475-21176717 | Common:2; Rare:110 | ||||
| chr13:21459167-21459507 | Common:1; Rare:123 | ||||
| chr13:21603811-21603885 | Rare:26 | ||||
| chr13:21604036-21604237 | Common:5; Rare:108 | ||||
| chr13:21670971-21671170 | Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:23889302-23889586 | Common:1; Rare:99 | ||||
| chr13:23979555-23979829 | Common:4; Rare:67 | ||||
| chr13:24160521-24160809 | Common:1; Rare:83 | ||||
| chr13:24512739-24512851 | Common:3; Rare:33 | ||||
| chr13:24922790-24923000 | Rare:61; Clinvar:1 | ||||
| chr13:25287235-25287572 | Common:2; Rare:106 |