| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18280228-18280450 | Common:4; Rare:88 | ||||
| chr19:18323024-18323302 | Common:3; Rare:90 | ||||
| chr19:18539423-18539624 | Common:4; Rare:63 | ||||
| chr19:18557646-18557904 | Common:5; Rare:70 | ||||
| chr19:18588713-18588835 | Rare:29 | ||||
| chr19:18919307-18919738 | Common:3; Rare:163 | ||||
| chr19:19033482-19033643 | Common:2; Rare:51 | ||||
| chr19:19192124-19192245 | Common:1; Rare:37 | ||||
| chr19:19192614-19192973 | Common:2; Rare:85 | ||||
| chr19:19320540-19320842 | Common:4; Rare:95 | ||||
| chr19:19516157-19516285 | Rare:79; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19900795-19900977 | Common:1; Rare:44 | ||||
| chr19:29213143-29213259 | Common:2; Rare:41 | ||||
| chr19:29665253-29665461 | Common:4; Rare:76 | ||||
| chr19:31349228-31349506 | Common:4; Rare:91 |