| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42302654-42302963 | Common:3; Rare:50 | ||||
| chr19:42390238-42390405 | Common:2; Rare:39 | ||||
| chr19:42423532-42423753 | Common:4; Rare:79 | ||||
| chr19:42442752-42443069 | Common:4; Rare:53 | ||||
| chr19:42528311-42528552 | Common:3; Rare:71; Clinvar:1 | ||||
| chr19:43463597-43464290 | Common:4; Rare:179 | ||||
| chr19:43465491-43465807 | Common:1; Rare:107 | ||||
| chr19:43504635-43504939 | Common:2; Rare:81 | ||||
| chr19:43527156-43527273 | Common:5; Rare:56; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43575433-43575767 | Common:2; Rare:101 | ||||
| chr19:43596045-43596433 | Common:3; Rare:121 | ||||
| chr19:43639786-43640069 | Common:1; Rare:78 | ||||
| chr19:43670116-43670306 | Common:2; Rare:47 | ||||
| chr19:43754840-43755106 | Common:3; Rare:103 | ||||
| chr19:43780962-43781096 | Rare:26 |