| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11200913-11201181 | Common:1; Rare:79 | ||||
| chr19:11223080-11223259 | Common:1; Rare:40; Clinvar (benign):1 | ||||
| chr19:11673855-11674032 | Rare:30 | ||||
| chr19:12194823-12195028 | Common:1; Rare:69 | ||||
| chr19:12675493-12675561 | Rare:23 | ||||
| chr19:12771233-12771474 | Rare:75 | ||||
| chr19:12790283-12790410 | Rare:26 | ||||
| chr19:12793490-12793765 | Common:3; Rare:75 | ||||
| chr19:12800982-12801163 | Common:1; Rare:57 | ||||
| chr19:13839259-13839307 | Common:1; Rare:8 | ||||
| chr19:13840505-13840895 | Common:1; Rare:84 | ||||
| chr19:14061977-14062409 | Common:7; Rare:93 | ||||
| chr19:14070070-14070337 | Common:3; Rare:50 | ||||
| chr19:14074205-14074402 | Rare:38 | ||||
| chr19:14164559-14164796 | Common:2; Rare:35 |