| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:97976319-97976773 | Common:2; Rare:173 | ||||
| chr13:98143345-98143481 | Common:3; Rare:31 | ||||
| chr13:98143945-98144060 | Rare:33 | ||||
| chr13:99200648-99200909 | Common:7; Rare:123 | ||||
| chr13:100088757-100089222 | Rare:176; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr13:100674759-100675024 | Common:3; Rare:104 | ||||
| chr13:100675075-100675159 | Common:1; Rare:32 | ||||
| chr13:102596759-102597068 | Common:1; Rare:134; Clinvar (benign):1 | ||||
| chr13:102798914-102799207 | Common:1; Rare:61 | ||||
| chr13:102800087-102800346 | Common:1; Rare:59 | ||||
| chr13:102845734-102846202 | Common:10; Rare:114; Clinvar:4; Clinvar (benign):6 | ||||
| chr13:102846239-102846354 | Rare:47; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr13:106567577-106567777 | Rare:64 | ||||
| chr13:106568038-106568292 | Rare:71 | ||||
| chr13:108215495-108215570 | Rare:19 |