| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10872134-10872390 | Rare:45 | ||||
| chr19:10919839-10919932 | Rare:22 | ||||
| chr19:10928498-10928919 | Common:2; Rare:138 | ||||
| chr19:10960602-10960915 | Common:7; Rare:118 | ||||
| chr19:10960917-10961265 | Rare:124; Clinvar (benign):2 | ||||
| chr19:11089069-11089103 | Rare:3 | ||||
| chr19:11089241-11089618 | Rare:79; Clinvar:17; Clinvar (benign):1; Clinvar (pathogenic):6 | ||||
| chr19:11090156-11090703 | Common:2; Rare:159 | ||||
| chr19:11155719-11156095 | Common:3; Rare:103 | ||||
| chr19:11197501-11198030 | Common:3; Rare:153 | ||||
| chr19:11262089-11262196 | Common:1; Rare:23 | ||||
| chr19:11262264-11262447 | Rare:43 | ||||
| chr19:11262449-11262592 | Common:1; Rare:51 | ||||
| chr19:11339581-11339821 | Common:5; Rare:64 | ||||
| chr19:11346161-11346782 | Rare:135 |