| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50514640-50514863 | Common:4; Rare:57 | ||||
| chr19:50804582-50804936 | Common:7; Rare:104 | ||||
| chr19:51311526-51311873 | Common:5; Rare:77 | ||||
| chr19:51366343-51366537 | Common:5; Rare:46; Clinvar (benign):2 | ||||
| chr19:51751857-51752098 | Common:2; Rare:56 | ||||
| chr19:51887858-51888046 | Rare:66 | ||||
| chr19:51904914-51905146 | Common:3; Rare:71 | ||||
| chr19:51927377-51927513 | Common:1; Rare:41 | ||||
| chr19:52008129-52008359 | Rare:69 | ||||
| chr19:52028111-52028235 | Rare:30 | ||||
| chr19:52028336-52028462 | Common:3; Rare:26 | ||||
| chr19:52028557-52028690 | Rare:23 | ||||
| chr19:52048736-52048908 | Common:1; Rare:62 | ||||
| chr19:52138775-52138894 | Rare:16 | ||||
| chr19:52171436-52171766 | Common:3; Rare:86 |