| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44141410-44141598 | Common:3; Rare:27 | ||||
| chr19:44164923-44165127 | Common:1; Rare:50 | ||||
| chr19:44914094-44914322 | Common:2; Rare:42 | ||||
| chr19:44955243-44955390 | Common:2; Rare:41 | ||||
| chr19:45038960-45039094 | Rare:44 | ||||
| chr19:45079143-45079347 | Rare:58 | ||||
| chr19:45406341-45406694 | Common:3; Rare:89 | ||||
| chr19:45423488-45423808 | Common:3; Rare:66; Clinvar (benign):1 | ||||
| chr19:45507228-45507510 | Common:1; Rare:72 | ||||
| chr19:45692381-45692713 | Common:1; Rare:76 | ||||
| chr19:46346951-46347117 | Common:3; Rare:48 | ||||
| chr19:46601172-46601411 | Common:3; Rare:71; Clinvar (benign):1 | ||||
| chr19:47256460-47256577 | Rare:45 | ||||
| chr19:48391486-48391694 | Rare:60 | ||||
| chr19:48445651-48445863 | Common:4; Rare:76 |