| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:108218294-108218512 | Common:1; Rare:79 | ||||
| chr13:109786574-109786879 | Common:1; Rare:107 | ||||
| chr13:110305523-110305757 | Common:1; Rare:36 | ||||
| chr13:110307087-110307514 | Common:6; Rare:135; Clinvar:1; Clinvar (benign):8 | ||||
| chr13:110429925-110430064 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr13:110712985-110713266 | Common:2; Rare:125 | ||||
| chr13:110713487-110713657 | Common:2; Rare:73 | ||||
| chr13:110715351-110715568 | Common:1; Rare:84 | ||||
| chr13:110715812-110715906 | Rare:71 | ||||
| chr13:110893291-110893451 | Common:1; Rare:37 | ||||
| chr13:110905844-110905966 | Rare:18 | ||||
| chr13:110914988-110915296 | Common:3; Rare:125 | ||||
| chr13:111153567-111153755 | Common:2; Rare:87 | ||||
| chr13:111202874-111203106 | Common:1; Rare:33 | ||||
| chr13:111204802-111205100 | Common:5; Rare:76 |