| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6502266-6502486 | Rare:58; Clinvar (benign):1 | ||||
| chr19:6530643-6530704 | Common:1; Rare:6 | ||||
| chr19:6530763-6531172 | Common:5; Rare:149 | ||||
| chr19:6590836-6591016 | Common:1; Rare:66 | ||||
| chr19:6736406-6736666 | Common:1; Rare:58 | ||||
| chr19:6737442-6737609 | Common:3; Rare:51 | ||||
| chr19:6738686-6738731 | Rare:8 | ||||
| chr19:6739500-6739764 | Common:6; Rare:80 | ||||
| chr19:6767987-6768100 | Common:1; Rare:22 | ||||
| chr19:6772493-6772747 | Rare:63 | ||||
| chr19:7069135-7069494 | Common:1; Rare:76 | ||||
| chr19:7069597-7069801 | Common:1; Rare:63 | ||||
| chr19:7294249-7294636 | Common:7; Rare:95 | ||||
| chr19:7394951-7395245 | Common:6; Rare:83 | ||||
| chr19:7488882-7489191 | Common:3; Rare:143 |