| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45091583-45091792 | Common:1; Rare:55 | ||||
| chr19:45092820-45093080 | Common:2; Rare:74 | ||||
| chr19:45370552-45370775 | Common:2; Rare:67 | ||||
| chr19:45406362-45406649 | Common:1; Rare:62 | ||||
| chr19:45507228-45507440 | Common:1; Rare:47 | ||||
| chr19:45584778-45585011 | Common:4; Rare:91; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:45643684-45643836 | Rare:32 | ||||
| chr19:45692372-45692713 | Common:1; Rare:79 | ||||
| chr19:45730860-45731043 | Common:1; Rare:39 | ||||
| chr19:46023050-46023212 | Common:2; Rare:36 | ||||
| chr19:46296841-46297062 | Common:4; Rare:80 | ||||
| chr19:46298120-46298439 | Common:5; Rare:76 | ||||
| chr19:46346939-46347117 | Common:3; Rare:54 | ||||
| chr19:46413539-46413764 | Common:1; Rare:73 | ||||
| chr19:46600908-46601416 | Common:5; Rare:175; Clinvar (benign):1 |