| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12681764-12681951 | Common:2; Rare:94; Clinvar (pathogenic):1 | ||||
| chr19:12696611-12696697 | Rare:42 | ||||
| chr19:12722482-12722757 | Common:3; Rare:45 | ||||
| chr19:12734338-12734828 | Common:1; Rare:159 | ||||
| chr19:12752388-12752709 | Common:3; Rare:89 | ||||
| chr19:12765976-12766209 | Common:3; Rare:84 | ||||
| chr19:12778405-12778541 | Common:2; Rare:26 | ||||
| chr19:12791260-12791832 | Common:2; Rare:138 | ||||
| chr19:12792230-12792855 | Common:3; Rare:142 | ||||
| chr19:12801754-12801945 | Common:1; Rare:66 | ||||
| chr19:12881434-12881585 | Rare:24 | ||||
| chr19:12933610-12933828 | Common:1; Rare:74 | ||||
| chr19:12938455-12938767 | Common:5; Rare:136 | ||||
| chr19:12945775-12945921 | Common:1; Rare:50 | ||||
| chr19:13102852-13102953 | Common:1; Rare:24 |