| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35869760-35869966 | Rare:69 | ||||
| chr19:35899712-35899863 | Common:1; Rare:46 | ||||
| chr19:35900538-35900696 | Rare:34 | ||||
| chr19:35994999-35995244 | Common:1; Rare:68; Clinvar (benign):1 | ||||
| chr19:36014167-36014573 | Common:2; Rare:114 | ||||
| chr19:36032670-36033090 | Common:5; Rare:90 | ||||
| chr19:36054029-36054190 | Rare:61 | ||||
| chr19:36054232-36054521 | Common:2; Rare:89 | ||||
| chr19:36054750-36054922 | Rare:49 | ||||
| chr19:36114793-36114949 | Common:1; Rare:71 | ||||
| chr19:36115189-36115569 | Common:3; Rare:121 | ||||
| chr19:36115653-36115798 | Rare:37 | ||||
| chr19:36139806-36140145 | Common:1; Rare:102 | ||||
| chr19:36140393-36141218 | Common:10; Rare:300 | ||||
| chr19:36214493-36214751 | Common:1; Rare:83 |