| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38769797-38770094 | Common:7; Rare:76 | ||||
| chr19:38831214-38831305 | Common:2; Rare:22 | ||||
| chr19:38831402-38831549 | Common:1; Rare:66; Clinvar (benign):1 | ||||
| chr19:38831733-38832085 | Common:4; Rare:117; Clinvar (benign):1 | ||||
| chr19:38849180-38849667 | Common:2; Rare:181 | ||||
| chr19:38849878-38850128 | Common:2; Rare:105 | ||||
| chr19:38850394-38850756 | Common:1; Rare:123 | ||||
| chr19:38850837-38850874 | Rare:8 | ||||
| chr19:38851792-38852156 | Common:3; Rare:129 | ||||
| chr19:38852623-38852785 | Common:1; Rare:38 | ||||
| chr19:38870055-38870183 | Common:1; Rare:46 | ||||
| chr19:38878158-38878473 | Common:2; Rare:56 | ||||
| chr19:38899554-38900063 | Rare:154 | ||||
| chr19:38900171-38900283 | Rare:24 | ||||
| chr19:38930306-38930560 | Common:1; Rare:97; Clinvar (benign):1 |