| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49869308-49869860 | Common:4; Rare:191 | ||||
| chr19:49871247-49871794 | Common:1; Rare:373 | ||||
| chr19:49890501-49891045 | Common:18; Rare:240 | ||||
| chr19:50050770-50051240 | Common:4; Rare:188 | ||||
| chr19:50147910-50148128 | Common:2; Rare:70 | ||||
| chr19:50173179-50173320 | Rare:21 | ||||
| chr19:50175940-50176340 | Common:9; Rare:117 | ||||
| chr19:50205197-50205566 | Common:2; Rare:174 | ||||
| chr19:50205789-50206189 | Common:3; Rare:124 | ||||
| chr19:50214688-50215650 | Common:13; Rare:326 | ||||
| chr19:50266962-50267161 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr19:50330684-50331047 | Common:4; Rare:138 | ||||
| chr19:50331082-50332215 | Common:17; Rare:228 | ||||
| chr19:50332176-50332576 | Common:3; Rare:80 | ||||
| chr19:50368493-50368970 | Common:3; Rare:138 |