| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44905320-44905887 | Common:4; Rare:149; Clinvar:1 | ||||
| chr19:44906496-44906748 | Common:1; Rare:89 | ||||
| chr19:44942087-44942340 | Common:3; Rare:55 | ||||
| chr19:44955242-44955432 | Common:2; Rare:61 | ||||
| chr19:45038965-45039104 | Rare:49 | ||||
| chr19:45079012-45079297 | Common:2; Rare:62 | ||||
| chr19:45092820-45092941 | Common:1; Rare:35 | ||||
| chr19:45406340-45406680 | Common:2; Rare:83 | ||||
| chr19:45423509-45423779 | Common:2; Rare:53; Clinvar (benign):1 | ||||
| chr19:45507228-45507517 | Common:1; Rare:75 | ||||
| chr19:45692434-45692713 | Common:1; Rare:64 | ||||
| chr19:45730857-45731047 | Common:1; Rare:40 | ||||
| chr19:45769194-45769390 | Rare:68 | ||||
| chr19:45863106-45863429 | Common:4; Rare:102 | ||||
| chr19:45864148-45864326 | Common:2; Rare:42 |