| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49867518-49867643 | Common:2; Rare:41; Clinvar:1 | ||||
| chr19:49877299-49877726 | Common:1; Rare:112 | ||||
| chr19:49877836-49878174 | Common:5; Rare:107 | ||||
| chr19:49928317-49928482 | Rare:49 | ||||
| chr19:49929073-49929212 | Common:3; Rare:44 | ||||
| chr19:49929216-49929550 | Common:3; Rare:112 | ||||
| chr19:49929918-49930219 | Common:1; Rare:72 | ||||
| chr19:50377600-50377851 | Common:1; Rare:98 | ||||
| chr19:50476240-50476550 | Rare:145 | ||||
| chr19:50804572-50804888 | Common:7; Rare:98 | ||||
| chr19:51124903-51124950 | Rare:16 | ||||
| chr19:51366271-51366595 | Common:8; Rare:101; Clinvar (benign):2 | ||||
| chr19:51751835-51751994 | Common:2; Rare:32 | ||||
| chr19:52008166-52008290 | Rare:38 | ||||
| chr19:52397733-52397879 | Common:2; Rare:43 |