| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:113490954-113491258 | Common:3; Rare:109 | ||||
| chr13:113584440-113584714 | Rare:78 | ||||
| chr13:114234788-114235203 | Common:16; Rare:144 | ||||
| chr13:114235307-114235390 | Rare:25 | ||||
| chr13:114281495-114281664 | Common:2; Rare:94 | ||||
| chr13:114281820-114282107 | Common:6; Rare:137 | ||||
| chr13:114282117-114282440 | Common:4; Rare:99 | ||||
| chr14:20343182-20343652 | Common:12; Rare:273 | ||||
| chr14:20413143-20413234 | Common:1; Rare:13 | ||||
| chr14:20413413-20413569 | Common:3; Rare:46 | ||||
| chr14:20454758-20455594 | Common:7; Rare:207 | ||||
| chr14:20461803-20461996 | Common:2; Rare:43 | ||||
| chr14:20684428-20684616 | Common:2; Rare:30; Clinvar (benign):2 | ||||
| chr14:20989736-20990029 | Common:6; Rare:72 | ||||
| chr14:21103976-21104098 | Rare:30 |