| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:3971071-3971359 | Common:1; Rare:85 | ||||
| chr19:3985414-3985609 | Common:1; Rare:111 | ||||
| chr19:5622753-5623161 | Common:5; Rare:150 | ||||
| chr19:5680468-5680594 | Rare:42 | ||||
| chr19:5978078-5978398 | Common:3; Rare:120 | ||||
| chr19:7395057-7395185 | Common:3; Rare:40 | ||||
| chr19:7489006-7489078 | Rare:34 | ||||
| chr19:7535543-7535747 | Common:3; Rare:69; Clinvar:2 | ||||
| chr19:7629538-7629859 | Common:5; Rare:113; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636989-7637143 | Common:2; Rare:51; Clinvar (benign):1 | ||||
| chr19:7903625-7903882 | Rare:79 | ||||
| chr19:7943630-7943976 | Rare:95 | ||||
| chr19:8005525-8005821 | Common:1; Rare:105 | ||||
| chr19:8321316-8321702 | Common:2; Rare:155 | ||||
| chr19:8390052-8390411 | Common:1; Rare:101 |