| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:2270117-2270321 | Common:2; Rare:57 | ||||
| chr19:2270770-2271055 | Common:7; Rare:103 | ||||
| chr19:2282147-2282270 | Common:2; Rare:33 | ||||
| chr19:2327779-2328026 | Common:2; Rare:45 | ||||
| chr19:2328516-2328789 | Common:3; Rare:133 | ||||
| chr19:2427094-2427234 | Common:4; Rare:52 | ||||
| chr19:2427505-2427716 | Common:3; Rare:98 | ||||
| chr19:2427836-2428025 | Common:4; Rare:76 | ||||
| chr19:2456592-2456767 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:2456871-2457170 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:2475844-2476330 | Common:3; Rare:156 | ||||
| chr19:2476594-2476653 | Rare:17 | ||||
| chr19:2739965-2740070 | Rare:42 | ||||
| chr19:2783223-2783694 | Common:1; Rare:132 | ||||
| chr19:2785224-2785648 | Common:5; Rare:129 |