| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6361472-6361766 | Common:1; Rare:110; Clinvar:2; Clinvar (benign):5 | ||||
| chr19:6372480-6372838 | Common:5; Rare:120 | ||||
| chr19:6373205-6373473 | Rare:35 | ||||
| chr19:6393040-6393320 | Common:5; Rare:76 | ||||
| chr19:6393369-6393759 | Common:5; Rare:114 | ||||
| chr19:6393911-6394011 | Rare:33 | ||||
| chr19:6424776-6425113 | Common:1; Rare:92 | ||||
| chr19:6459751-6459942 | Common:3; Rare:50 | ||||
| chr19:6476576-6476885 | Common:5; Rare:81 | ||||
| chr19:6502140-6502540 | Rare:103; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr19:6530868-6531036 | Common:3; Rare:67 | ||||
| chr19:6591138-6591423 | Common:1; Rare:45 | ||||
| chr19:6736504-6736917 | Common:2; Rare:238 | ||||
| chr19:6737696-6738048 | Common:5; Rare:83 | ||||
| chr19:6738465-6738865 | Common:1; Rare:97 |