| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46104135-46104420 | Common:4; Rare:85; Clinvar (benign):1 | ||||
| chr18:46917370-46917659 | Common:3; Rare:123 | ||||
| chr18:47150435-47150570 | Common:3; Rare:51 | ||||
| chr18:48137041-48137202 | Rare:32 | ||||
| chr18:49460577-49460889 | Common:2; Rare:99; Clinvar:4; Clinvar (benign):1 | ||||
| chr18:49487043-49487328 | Common:3; Rare:108 | ||||
| chr18:49490452-49490920 | Common:1; Rare:114 | ||||
| chr18:49560991-49561037 | Rare:14 | ||||
| chr18:49561860-49562077 | Rare:61 | ||||
| chr18:49813508-49813638 | Rare:28 | ||||
| chr18:49813826-49814330 | Common:2; Rare:200 | ||||
| chr18:49849779-49850008 | Common:1; Rare:54 | ||||
| chr18:50281395-50281890 | Common:3; Rare:164 | ||||
| chr18:50374876-50375150 | Common:4; Rare:88 | ||||
| chr18:50878936-50879264 | Common:4; Rare:108 |