| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48811003-48811023 | Rare:6 | ||||
| chr19:48811025-48811058 | Rare:12 | ||||
| chr19:48933588-48933713 | Common:3; Rare:43 | ||||
| chr19:48954720-48954925 | Rare:73 | ||||
| chr19:48965273-48965926 | Common:1; Rare:230; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):8 | ||||
| chr19:48993253-48993540 | Common:3; Rare:129; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:48993740-48993920 | Common:4; Rare:55 | ||||
| chr19:49085396-49085622 | Common:1; Rare:99 | ||||
| chr19:49114234-49114402 | Common:2; Rare:44 | ||||
| chr19:49157717-49157878 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:49335404-49335506 | Common:1; Rare:26 | ||||
| chr19:49335583-49335693 | Common:1; Rare:39 | ||||
| chr19:49489589-49489921 | Common:1; Rare:104 | ||||
| chr19:49496266-49496470 | Common:1; Rare:76 | ||||
| chr19:49513102-49513467 | Common:1; Rare:78 |