| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:54159409-54159566 | Common:1; Rare:68 | ||||
| chr19:54159601-54160328 | Common:2; Rare:228 | ||||
| chr19:54160345-54160367 | Rare:4 | ||||
| chr19:54160457-54160540 | Common:1; Rare:24 | ||||
| chr19:54172805-54172964 | Rare:39 | ||||
| chr19:54172996-54173258 | Common:3; Rare:75 | ||||
| chr19:54189191-54189393 | Common:1; Rare:46 | ||||
| chr19:54189414-54189536 | Common:1; Rare:37 | ||||
| chr19:54189541-54189994 | Common:4; Rare:125 | ||||
| chr19:54190045-54190185 | Common:1; Rare:37 | ||||
| chr19:54190219-54190447 | Common:2; Rare:74; Clinvar:1 | ||||
| chr19:54190455-54190756 | Common:5; Rare:85; Clinvar (benign):1 | ||||
| chr19:54190860-54191057 | Rare:65 | ||||
| chr19:54191139-54191374 | Common:4; Rare:89; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:54191484-54191611 | Rare:47; Clinvar (benign):1 |