| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:108215495-108215707 | Common:1; Rare:55 | ||||
| chr13:108218339-108218520 | Rare:71 | ||||
| chr13:110713018-110713266 | Common:2; Rare:108 | ||||
| chr13:111153622-111153720 | Common:2; Rare:43 | ||||
| chr13:111202904-111203093 | Common:1; Rare:26 | ||||
| chr13:112588066-112588197 | Rare:38 | ||||
| chr13:113208625-113208743 | Rare:71 | ||||
| chr13:114281480-114281650 | Common:2; Rare:86 | ||||
| chr13:114281815-114282091 | Common:6; Rare:134 | ||||
| chr13:114282102-114282430 | Common:4; Rare:100 | ||||
| chr14:20343205-20343642 | Common:12; Rare:256 | ||||
| chr14:20413425-20413562 | Common:3; Rare:43 | ||||
| chr14:20454793-20455287 | Common:7; Rare:130 | ||||
| chr14:20684447-20684614 | Common:1; Rare:28; Clinvar (benign):1 | ||||
| chr14:21476950-21477271 | Common:1; Rare:96 |