| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50476600-50477110 | Rare:161 | ||||
| chr19:50511117-50511585 | Common:3; Rare:202 | ||||
| chr19:50804051-50804387 | Common:4; Rare:118 | ||||
| chr19:50804452-50804985 | Common:14; Rare:240 | ||||
| chr19:50804890-50805200 | Common:6; Rare:84 | ||||
| chr19:51108360-51108597 | Common:1; Rare:53 | ||||
| chr19:51225015-51225115 | Rare:26 | ||||
| chr19:51225024-51225124 | Rare:26 | ||||
| chr19:51339650-51340090 | Common:2; Rare:153 | ||||
| chr19:51366309-51366588 | Common:16; Rare:157; Clinvar (benign):4 | ||||
| chr19:51367503-51367909 | Common:6; Rare:243 | ||||
| chr19:51368000-51368400 | Common:2; Rare:184 | ||||
| chr19:51570990-51571400 | Common:6; Rare:103 | ||||
| chr19:51986788-51986921 | Common:1; Rare:41 | ||||
| chr19:52008030-52008500 | Common:2; Rare:146 |