| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10960559-10961467 | Common:33; Rare:1258; Clinvar (benign):2 | ||||
| chr19:10961498-10962179 | Common:5; Rare:176 | ||||
| chr19:10983930-10984330 | Rare:109; Clinvar:23; Clinvar (benign):13 | ||||
| chr19:11088846-11089597 | Rare:445; Clinvar:83; Clinvar (benign):3; Clinvar (pathogenic):19 | ||||
| chr19:11090124-11090644 | Common:17; Rare:798 | ||||
| chr19:11155700-11156240 | Common:21; Rare:635 | ||||
| chr19:11197387-11197787 | Common:8; Rare:382 | ||||
| chr19:11197737-11198070 | Common:6; Rare:323 | ||||
| chr19:11203518-11203918 | Rare:90 | ||||
| chr19:11262320-11262720 | Common:4; Rare:247 | ||||
| chr19:11339499-11339899 | Common:10; Rare:181 | ||||
| chr19:11344324-11344724 | Common:3; Rare:98 | ||||
| chr19:11346031-11346800 | Rare:745 | ||||
| chr19:11346898-11347013 | Common:1; Rare:15 | ||||
| chr19:11355136-11355502 | Common:2; Rare:149 |