| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48933370-48933780 | Common:8; Rare:152 | ||||
| chr19:48954691-48954960 | Rare:180 | ||||
| chr19:48964816-48965489 | Common:2; Rare:241; Clinvar:2; Clinvar (pathogenic):5 | ||||
| chr19:48993142-48993930 | Common:18; Rare:520; Clinvar:6; Clinvar (benign):6 | ||||
| chr19:49085088-49085634 | Common:6; Rare:395 | ||||
| chr19:49118590-49118930 | Common:6; Rare:272 | ||||
| chr19:49118940-49119500 | Common:1; Rare:260 | ||||
| chr19:49127930-49128370 | Common:4; Rare:195 | ||||
| chr19:49157520-49157880 | Common:4; Rare:180; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:49361430-49361720 | Common:2; Rare:98 | ||||
| chr19:49362279-49362545 | Common:1; Rare:59 | ||||
| chr19:49451754-49452022 | Common:6; Rare:133 | ||||
| chr19:49453049-49453325 | Common:2; Rare:170 | ||||
| chr19:49453443-49453669 | Common:2; Rare:148 | ||||
| chr19:49474055-49474275 | Common:2; Rare:108 |