| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:114234835-114235136 | Common:14; Rare:106 | ||||
| chr13:114281299-114282105 | Common:12; Rare:376 | ||||
| chr14:20305933-20306037 | Rare:32 | ||||
| chr14:20333264-20333429 | Common:1; Rare:33 | ||||
| chr14:20343184-20343679 | Common:12; Rare:296 | ||||
| chr14:20454722-20455343 | Common:7; Rare:164 | ||||
| chr14:20455359-20455585 | Rare:55 | ||||
| chr14:20461739-20462031 | Common:2; Rare:69 | ||||
| chr14:20469165-20469451 | Common:2; Rare:60; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:20989665-20990036 | Common:7; Rare:92 | ||||
| chr14:21104011-21104132 | Common:1; Rare:35 | ||||
| chr14:21269320-21269958 | Common:4; Rare:214 | ||||
| chr14:21383871-21384055 | Common:1; Rare:64 | ||||
| chr14:21384223-21384425 | Rare:72 | ||||
| chr14:21437212-21437408 | Common:4; Rare:81 |