| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1383373-1383676 | Common:3; Rare:206 | ||||
| chr19:1401488-1401640 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:1407180-1407670 | Common:3; Rare:204 | ||||
| chr19:1438224-1438450 | Common:1; Rare:86 | ||||
| chr19:1438767-1439167 | Common:3; Rare:165; Clinvar (benign):2 | ||||
| chr19:1446020-1446320 | Common:2; Rare:79 | ||||
| chr19:1449810-1450280 | Common:2; Rare:137 | ||||
| chr19:1479179-1479354 | Common:1; Rare:61 | ||||
| chr19:1490293-1490511 | Common:3; Rare:77 | ||||
| chr19:1490701-1491021 | Common:5; Rare:88 | ||||
| chr19:1507710-1508080 | Common:1; Rare:133 | ||||
| chr19:1568280-1568570 | Common:3; Rare:113 | ||||
| chr19:1592274-1592532 | Rare:145 | ||||
| chr19:1592680-1593250 | Common:2; Rare:240 | ||||
| chr19:1605405-1605699 | Common:3; Rare:115 |