| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44905580-44905834 | Rare:77 | ||||
| chr19:44955237-44955395 | Common:2; Rare:46 | ||||
| chr19:45038960-45039094 | Rare:44 | ||||
| chr19:45092822-45092953 | Common:1; Rare:40 | ||||
| chr19:45370548-45370731 | Common:2; Rare:53 | ||||
| chr19:45406363-45406663 | Common:1; Rare:70 | ||||
| chr19:45423512-45423648 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chr19:45692383-45692700 | Common:1; Rare:71 | ||||
| chr19:45730869-45731103 | Common:1; Rare:54 | ||||
| chr19:46346864-46347119 | Common:3; Rare:83 | ||||
| chr19:46471521-46471702 | Common:2; Rare:63 | ||||
| chr19:46600994-46601431 | Common:5; Rare:148; Clinvar (benign):3 | ||||
| chr19:46746024-46746061 | Common:2; Rare:13 | ||||
| chr19:46788572-46788649 | Rare:20 | ||||
| chr19:47112151-47112352 | Rare:59 |