| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58499206-58499634 | Common:2; Rare:152; Clinvar:6; Clinvar (benign):1 | ||||
| chr19:58519760-58520011 | Rare:66 | ||||
| chr19:58554939-58555157 | Common:1; Rare:73 | ||||
| chr19:58573305-58573499 | Rare:47 | ||||
| chr19:58573534-58573685 | Common:2; Rare:40 | ||||
| chr2:263989-264070 | Common:1; Rare:33 | ||||
| chr2:677352-677557 | Common:1; Rare:87 | ||||
| chr2:2324310-2324659 | Rare:68 | ||||
| chr2:2324774-2324906 | Common:1; Rare:27 | ||||
| chr2:2324929-2325159 | Common:1; Rare:45 | ||||
| chr2:2331064-2331415 | Common:3; Rare:70 | ||||
| chr2:3377774-3377953 | Rare:52 | ||||
| chr2:3379619-3379767 | Common:1; Rare:61 | ||||
| chr2:3519516-3519685 | Common:2; Rare:42 | ||||
| chr2:3558256-3558565 | Common:6; Rare:116 |