| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45370553-45370790 | Common:2; Rare:70 | ||||
| chr19:45406290-45406670 | Common:1; Rare:86 | ||||
| chr19:45423433-45423670 | Common:3; Rare:51; Clinvar (benign):2 | ||||
| chr19:45507386-45507516 | Rare:39 | ||||
| chr19:45692374-45692722 | Common:1; Rare:84 | ||||
| chr19:45730869-45731052 | Common:1; Rare:39 | ||||
| chr19:45768251-45768329 | Rare:34; Clinvar (benign):1 | ||||
| chr19:45769203-45769325 | Rare:35 | ||||
| chr19:46296832-46297079 | Common:4; Rare:94 | ||||
| chr19:46298059-46298480 | Common:5; Rare:97 | ||||
| chr19:46303458-46303662 | Common:1; Rare:36 | ||||
| chr19:46346938-46347143 | Common:3; Rare:69 | ||||
| chr19:46600907-46601434 | Common:6; Rare:181; Clinvar (benign):3 | ||||
| chr19:46745969-46746074 | Common:3; Rare:27 | ||||
| chr19:47112146-47112570 | Rare:142 |