| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44778236-44778286 | Rare:17 | ||||
| chr19:44954396-44954604 | Common:2; Rare:52 | ||||
| chr19:44954924-44955028 | Common:2; Rare:30 | ||||
| chr19:45079040-45079317 | Common:1; Rare:66 | ||||
| chr19:45091583-45091788 | Common:1; Rare:53 | ||||
| chr19:45406290-45406649 | Common:1; Rare:77 | ||||
| chr19:45507312-45507535 | Rare:69 | ||||
| chr19:45692365-45692691 | Common:1; Rare:74 | ||||
| chr19:45730867-45731003 | Common:1; Rare:26 | ||||
| chr19:45769145-45769326 | Rare:52 | ||||
| chr19:45864148-45864326 | Common:2; Rare:42 | ||||
| chr19:46296836-46297065 | Common:4; Rare:87 | ||||
| chr19:46303480-46303675 | Common:1; Rare:36 | ||||
| chr19:46346951-46347148 | Common:3; Rare:67 | ||||
| chr19:46601188-46601420 | Common:3; Rare:69; Clinvar (benign):1 |