| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12666365-12666525 | Rare:33 | ||||
| chr19:12666662-12666891 | Rare:91; Clinvar:4 | ||||
| chr19:12669348-12669763 | Common:5; Rare:145 | ||||
| chr19:12681198-12681666 | Common:2; Rare:168 | ||||
| chr19:12681735-12682099 | Common:4; Rare:151; Clinvar (pathogenic):1 | ||||
| chr19:12696568-12696753 | Rare:86 | ||||
| chr19:12721975-12722225 | Rare:39 | ||||
| chr19:12722662-12722905 | Common:1; Rare:53 | ||||
| chr19:12722970-12723085 | Rare:26 | ||||
| chr19:12723865-12724104 | Common:1; Rare:60 | ||||
| chr19:12734560-12734909 | Common:1; Rare:126 | ||||
| chr19:12736816-12737137 | Common:1; Rare:74 | ||||
| chr19:12737162-12737587 | Rare:105 | ||||
| chr19:12775513-12775806 | Common:3; Rare:75 | ||||
| chr19:12778051-12778572 | Common:3; Rare:95 |