| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:113759030-113759296 | Common:3; Rare:65 | ||||
| chr13:113863835-113864175 | Common:3; Rare:83 | ||||
| chr13:114132494-114132810 | Common:1; Rare:102 | ||||
| chr13:114281295-114281654 | Common:5; Rare:141 | ||||
| chr13:114281808-114282073 | Common:6; Rare:132 | ||||
| chr13:114282080-114282402 | Common:4; Rare:98 | ||||
| chr14:20343174-20343644 | Common:12; Rare:276 | ||||
| chr14:20413413-20413558 | Common:3; Rare:45 | ||||
| chr14:20454768-20455287 | Common:7; Rare:137 | ||||
| chr14:20455510-20455594 | Rare:19 | ||||
| chr14:20461739-20462016 | Common:2; Rare:64 | ||||
| chr14:20469929-20470194 | Common:1; Rare:40 | ||||
| chr14:20684428-20684752 | Common:3; Rare:60; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:20802795-20802970 | Common:1; Rare:23 | ||||
| chr14:20989674-20990005 | Common:7; Rare:74 |