| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38724152-38724566 | Common:2; Rare:137; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:38831840-38832169 | Common:6; Rare:78 | ||||
| chr19:38841914-38842069 | Rare:36 | ||||
| chr19:38842209-38842477 | Rare:56 | ||||
| chr19:38842690-38842713 | Rare:5 | ||||
| chr19:38847324-38847567 | Common:3; Rare:66 | ||||
| chr19:38849700-38849747 | Common:1; Rare:15 | ||||
| chr19:38852315-38852458 | Rare:43 | ||||
| chr19:38899506-38900206 | Rare:194 | ||||
| chr19:38930715-38931053 | Common:3; Rare:99; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39156556-39156704 | Common:2; Rare:30 | ||||
| chr19:39342358-39342527 | Common:2; Rare:54 | ||||
| chr19:39390817-39391425 | Common:1; Rare:227; Clinvar:1 | ||||
| chr19:39406572-39406929 | Common:1; Rare:108 | ||||
| chr19:39407703-39407740 | Rare:12 |