| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:46600973-46601409 | Common:4; Rare:149; Clinvar (benign):1 | ||||
| chr19:46608292-46608496 | Common:1; Rare:54; Clinvar (benign):4 | ||||
| chr19:46717047-46717252 | Common:3; Rare:69 | ||||
| chr19:46745971-46746061 | Common:3; Rare:24 | ||||
| chr19:46746306-46746583 | Common:4; Rare:83 | ||||
| chr19:46787270-46787531 | Common:1; Rare:72 | ||||
| chr19:46788555-46788731 | Rare:41 | ||||
| chr19:46850245-46850383 | Rare:19 | ||||
| chr19:47112151-47112335 | Rare:52 | ||||
| chr19:47113109-47113435 | Common:2; Rare:88 | ||||
| chr19:47113774-47113911 | Common:1; Rare:31 | ||||
| chr19:47256472-47256596 | Rare:45 | ||||
| chr19:47309685-47309898 | Common:1; Rare:45 | ||||
| chr19:47332074-47332198 | Rare:18 | ||||
| chr19:47484209-47484310 | Common:1; Rare:28 |