| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1272564-1273159 | Common:6; Rare:498 | ||||
| chr19:1273504-1273904 | Common:2; Rare:129 | ||||
| chr19:1274468-1275159 | Common:12; Rare:523 | ||||
| chr19:1275220-1276142 | Common:17; Rare:2005 | ||||
| chr19:1354689-1355119 | Common:18; Rare:898 | ||||
| chr19:1383250-1384150 | Common:17; Rare:1727; Clinvar (benign):10 | ||||
| chr19:1401290-1401700 | Common:5; Rare:269; Clinvar:20; Clinvar (benign):22; Clinvar (pathogenic):2 | ||||
| chr19:1407138-1408062 | Common:21; Rare:1603 | ||||
| chr19:1415325-1415804 | Common:14; Rare:163 | ||||
| chr19:1438115-1438515 | Common:5; Rare:534 | ||||
| chr19:1438739-1439139 | Common:4; Rare:192; Clinvar (benign):2 | ||||
| chr19:1445490-1445810 | Common:3; Rare:79 | ||||
| chr19:1478142-1478977 | Common:10; Rare:467 | ||||
| chr19:1479063-1479463 | Common:6; Rare:546 | ||||
| chr19:1479390-1479790 | Common:11; Rare:402 |