| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10315872-10316262 | Common:4; Rare:140; Clinvar (benign):9 | ||||
| chr19:10333504-10333701 | Rare:64 | ||||
| chr19:10353625-10353686 | Rare:14; Clinvar (pathogenic):1 | ||||
| chr19:10565995-10566314 | Common:2; Rare:92 | ||||
| chr19:10568974-10569221 | Common:2; Rare:64 | ||||
| chr19:10653825-10653887 | Rare:23 | ||||
| chr19:10836185-10836551 | Common:2; Rare:98 | ||||
| chr19:10928599-10928795 | Common:1; Rare:52 | ||||
| chr19:10960668-10961087 | Common:6; Rare:175 | ||||
| chr19:11155772-11156062 | Common:3; Rare:67 | ||||
| chr19:11197483-11197687 | Common:1; Rare:62 | ||||
| chr19:11197725-11197912 | Common:2; Rare:51 | ||||
| chr19:11203404-11204061 | Rare:144 | ||||
| chr19:11374556-11374737 | Common:1; Rare:61 | ||||
| chr19:11419287-11419472 | Rare:38 |