| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41860733-41860814 | Rare:34; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:41860822-41860963 | Common:2; Rare:38; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:41882995-41883014 | Rare:4 | ||||
| chr19:41883066-41883248 | Common:1; Rare:36 | ||||
| chr19:41884094-41884492 | Rare:108 | ||||
| chr19:41928249-41928341 | Rare:21 | ||||
| chr19:41958375-41958798 | Common:3; Rare:136 | ||||
| chr19:41959248-41959490 | Common:1; Rare:80 | ||||
| chr19:42070079-42070095 | Rare:3 | ||||
| chr19:42070107-42070219 | Rare:38 | ||||
| chr19:42075711-42076296 | Common:5; Rare:168 | ||||
| chr19:42076367-42076388 | Rare:4 | ||||
| chr19:42216909-42217280 | Rare:122 | ||||
| chr19:42217629-42218099 | Common:2; Rare:145 | ||||
| chr19:42218147-42218286 | Rare:24 |