| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18543516-18543718 | Common:2; Rare:38 | ||||
| chr19:18544008-18544166 | Common:1; Rare:26 | ||||
| chr19:18557613-18557993 | Common:5; Rare:98 | ||||
| chr19:18571361-18571436 | Rare:14 | ||||
| chr19:18571474-18571927 | Common:6; Rare:159 | ||||
| chr19:18572406-18572610 | Common:2; Rare:40 | ||||
| chr19:18588095-18588301 | Rare:31 | ||||
| chr19:18588676-18588880 | Common:1; Rare:53 | ||||
| chr19:18588998-18589278 | Common:3; Rare:101 | ||||
| chr19:18589367-18589675 | Common:1; Rare:99 | ||||
| chr19:18589886-18589982 | Common:1; Rare:16 | ||||
| chr19:18594346-18594509 | Common:1; Rare:48; Clinvar (pathogenic):1 | ||||
| chr19:18636720-18637109 | Common:2; Rare:99 | ||||
| chr19:18683371-18683736 | Common:2; Rare:102 | ||||
| chr19:18831746-18832059 | Common:2; Rare:111 |