| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7629529-7629844 | Common:5; Rare:113; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7943627-7943988 | Rare:102 | ||||
| chr19:8321318-8321619 | Common:2; Rare:131 | ||||
| chr19:8390036-8390419 | Common:1; Rare:107 | ||||
| chr19:8444832-8445040 | Common:2; Rare:93 | ||||
| chr19:8514149-8514227 | Common:1; Rare:20 | ||||
| chr19:9435559-9435598 | Rare:14 | ||||
| chr19:9538603-9538716 | Common:1; Rare:33 | ||||
| chr19:9621192-9621529 | Common:3; Rare:94 | ||||
| chr19:9818811-9818858 | Rare:18 | ||||
| chr19:9827833-9827954 | Common:1; Rare:47 | ||||
| chr19:9835044-9835347 | Rare:124 | ||||
| chr19:10333516-10333709 | Rare:64 | ||||
| chr19:11089303-11089494 | Rare:26; Clinvar:8; Clinvar (pathogenic):1 | ||||
| chr19:11197504-11197622 | Common:1; Rare:32 |