| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18683524-18683688 | Common:1; Rare:53 | ||||
| chr19:18919328-18919744 | Common:2; Rare:154 | ||||
| chr19:18941239-18941449 | Common:4; Rare:55 | ||||
| chr19:19033443-19033754 | Common:2; Rare:99 | ||||
| chr19:19033822-19033929 | Common:1; Rare:30 | ||||
| chr19:19138426-19138493 | Common:1; Rare:29 | ||||
| chr19:19192098-19192268 | Common:1; Rare:55 | ||||
| chr19:19192574-19193008 | Common:3; Rare:110; Clinvar (benign):1 | ||||
| chr19:19203270-19203443 | Common:1; Rare:52 | ||||
| chr19:19320476-19320850 | Common:4; Rare:136 | ||||
| chr19:19516163-19516306 | Rare:86; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19528158-19528447 | Rare:63 | ||||
| chr19:19628485-19628699 | Rare:40 | ||||
| chr19:19643591-19643736 | Common:3; Rare:44 | ||||
| chr19:19668687-19668849 | Common:1; Rare:46 |