| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:111153569-111153720 | Common:2; Rare:69 | ||||
| chr13:111202922-111203064 | Common:1; Rare:19 | ||||
| chr13:112969135-112969382 | Common:2; Rare:66 | ||||
| chr13:113208640-113208751 | Rare:59 | ||||
| chr13:113584494-113584712 | Rare:60 | ||||
| chr13:114281319-114281654 | Common:5; Rare:133 | ||||
| chr14:20343161-20343644 | Common:13; Rare:282 | ||||
| chr14:20413420-20413509 | Common:2; Rare:21 | ||||
| chr14:20454804-20455287 | Common:7; Rare:127 | ||||
| chr14:20684437-20684683 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:21025692-21025865 | Common:2; Rare:32 | ||||
| chr14:21383931-21384052 | Common:1; Rare:50 | ||||
| chr14:21456042-21456271 | Common:4; Rare:61 | ||||
| chr14:21476843-21477275 | Common:2; Rare:143 | ||||
| chr14:21511300-21511549 | Rare:63 |