| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10194320-10194883 | Common:10; Rare:358; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:10194846-10195280 | Common:4; Rare:428; Clinvar (benign):7 | ||||
| chr19:10231164-10231801 | Common:4; Rare:200 | ||||
| chr19:10251733-10252053 | Common:5; Rare:208 | ||||
| chr19:10252114-10252299 | Common:2; Rare:84 | ||||
| chr19:10270935-10271176 | Common:1; Rare:150 | ||||
| chr19:10289030-10289701 | Common:7; Rare:197 | ||||
| chr19:10315160-10315560 | Common:12; Rare:214; Clinvar (benign):2 | ||||
| chr19:10315706-10316106 | Common:13; Rare:321; Clinvar (benign):23 | ||||
| chr19:10333069-10333348 | Rare:165 | ||||
| chr19:10333422-10333819 | Common:3; Rare:317 | ||||
| chr19:10334742-10335143 | Common:3; Rare:145 | ||||
| chr19:10380381-10380972 | Common:39; Rare:420; Clinvar:15 | ||||
| chr19:10395730-10396000 | Common:6; Rare:169 | ||||
| chr19:10403430-10403850 | Rare:401 |