| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:14529329-14529635 | Common:1; Rare:135 | ||||
| chr19:14776833-14777112 | Common:4; Rare:58 | ||||
| chr19:15200796-15201112 | Common:1; Rare:76 | ||||
| chr19:15332297-15332634 | Common:1; Rare:124 | ||||
| chr19:16076207-16076696 | Common:2; Rare:132 | ||||
| chr19:16197736-16198010 | Common:3; Rare:97 | ||||
| chr19:16542399-16542537 | Common:2; Rare:35 | ||||
| chr19:16660102-16660388 | Common:3; Rare:106 | ||||
| chr19:16661068-16661204 | Common:1; Rare:47 | ||||
| chr19:17075622-17075858 | Common:5; Rare:94 | ||||
| chr19:17405394-17405826 | Common:5; Rare:97 | ||||
| chr19:17847960-17848150 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:18152996-18153287 | Common:1; Rare:97 | ||||
| chr19:18280595-18280620 | Rare:7 | ||||
| chr19:18323056-18323307 | Common:3; Rare:69 |