| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39386724-39386912 | Rare:45 | ||||
| chr19:39390850-39391435 | Common:1; Rare:222 | ||||
| chr19:39406684-39406931 | Rare:94 | ||||
| chr19:39407035-39407347 | Rare:63 | ||||
| chr19:39407426-39407924 | Common:1; Rare:131 | ||||
| chr19:39435846-39436167 | Common:7; Rare:118 | ||||
| chr19:39480716-39480937 | Common:3; Rare:114; Clinvar (pathogenic):1 | ||||
| chr19:39846309-39846470 | Common:1; Rare:75 | ||||
| chr19:39970918-39971214 | Common:4; Rare:82 | ||||
| chr19:39996947-39997118 | Common:5; Rare:58 | ||||
| chr19:40056144-40056255 | Rare:15 | ||||
| chr19:40090865-40090990 | Common:1; Rare:36 | ||||
| chr19:40348388-40348724 | Common:4; Rare:110 | ||||
| chr19:40425963-40426141 | Common:1; Rare:59 | ||||
| chr19:40444283-40444518 | Common:3; Rare:74 |