| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50384005-50384393 | Common:5; Rare:317; Clinvar:3; Clinvar (benign):4 | ||||
| chr19:50511000-50511600 | Common:7; Rare:291 | ||||
| chr19:50804570-50805123 | Common:19; Rare:309 | ||||
| chr19:51339680-51340220 | Common:2; Rare:182 | ||||
| chr19:51342116-51342536 | Common:3; Rare:70 | ||||
| chr19:51366275-51366640 | Common:16; Rare:207; Clinvar (benign):4 | ||||
| chr19:51367532-51367899 | Common:2; Rare:227 | ||||
| chr19:51367960-51368480 | Common:2; Rare:206 | ||||
| chr19:51927230-51927640 | Common:2; Rare:205 | ||||
| chr19:51986773-51987025 | Common:1; Rare:71 | ||||
| chr19:52008164-52008312 | Rare:83 | ||||
| chr19:52028324-52028486 | Common:6; Rare:64 | ||||
| chr19:52048430-52048680 | Common:1; Rare:42 | ||||
| chr19:52095700-52096033 | Common:4; Rare:130 | ||||
| chr19:52138840-52139460 | Common:6; Rare:149 |