| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:113490682-113491268 | Common:4; Rare:209 | ||||
| chr13:113759066-113759288 | Common:1; Rare:60 | ||||
| chr13:113863832-113864191 | Common:3; Rare:88 | ||||
| chr13:114281480-114281682 | Common:2; Rare:111 | ||||
| chr13:114282117-114282430 | Common:4; Rare:95 | ||||
| chr14:20343184-20343655 | Common:12; Rare:274 | ||||
| chr14:20413143-20413224 | Common:1; Rare:11 | ||||
| chr14:20413415-20413520 | Common:2; Rare:29 | ||||
| chr14:20454738-20455305 | Common:7; Rare:150 | ||||
| chr14:20455359-20455698 | Rare:95 | ||||
| chr14:20684016-20684244 | Common:11; Rare:117; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:20684429-20684629 | Common:2; Rare:31; Clinvar (benign):2 | ||||
| chr14:20781197-20781337 | Rare:23 | ||||
| chr14:20802795-20802973 | Common:1; Rare:23 | ||||
| chr14:20955337-20955523 | Common:1; Rare:34 |