| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1383569-1383989 | Common:1; Rare:234; Clinvar (benign):2 | ||||
| chr19:1401452-1401633 | Common:1; Rare:51; Clinvar:4; Clinvar (benign):6 | ||||
| chr19:1407152-1407607 | Common:3; Rare:187 | ||||
| chr19:1407660-1408120 | Common:2; Rare:132 | ||||
| chr19:1438225-1438533 | Common:1; Rare:129 | ||||
| chr19:1479094-1479360 | Common:1; Rare:98 | ||||
| chr19:1479483-1479668 | Common:1; Rare:46 | ||||
| chr19:1490280-1490510 | Common:4; Rare:83 | ||||
| chr19:1512985-1513176 | Common:1; Rare:69 | ||||
| chr19:1568334-1568570 | Common:3; Rare:87 | ||||
| chr19:1592253-1592599 | Rare:183 | ||||
| chr19:1592729-1593122 | Common:1; Rare:186 | ||||
| chr19:1605354-1605708 | Common:3; Rare:134 | ||||
| chr19:1605926-1605964 | Rare:10 | ||||
| chr19:1651327-1651616 | Common:2; Rare:117 |