| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:46717053-46717271 | Common:2; Rare:74 | ||||
| chr19:46745825-46746107 | Common:3; Rare:73; Clinvar (benign):3 | ||||
| chr19:46746376-46746622 | Common:3; Rare:81 | ||||
| chr19:46784389-46784482 | Common:1; Rare:16 | ||||
| chr19:46784486-46784762 | Common:5; Rare:91 | ||||
| chr19:46784766-46785093 | Common:1; Rare:71 | ||||
| chr19:46786668-46786876 | Common:2; Rare:44 | ||||
| chr19:46787245-46787450 | Common:1; Rare:52 | ||||
| chr19:46787452-46787682 | Rare:76 | ||||
| chr19:46788457-46788895 | Common:2; Rare:100 | ||||
| chr19:46850239-46850494 | Rare:35 | ||||
| chr19:46850598-46850708 | Rare:29 | ||||
| chr19:46850740-46850882 | Rare:42 | ||||
| chr19:47035874-47036039 | Rare:49 | ||||
| chr19:47048250-47048294 | Common:1; Rare:14 |