| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1275372-1275726 | Rare:186 | ||||
| chr19:1275729-1276137 | Common:2; Rare:187 | ||||
| chr19:1354786-1355020 | Common:3; Rare:107 | ||||
| chr19:1401517-1401586 | Common:1; Rare:23; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:1438271-1438448 | Rare:71 | ||||
| chr19:1479544-1479611 | Rare:17 | ||||
| chr19:1605362-1605626 | Common:3; Rare:102 | ||||
| chr19:1812228-1812508 | Common:2; Rare:79 | ||||
| chr19:1941376-1941413 | Rare:12 | ||||
| chr19:2015318-2015538 | Rare:73 | ||||
| chr19:2051241-2051436 | Common:2; Rare:79 | ||||
| chr19:2096229-2096397 | Rare:58 | ||||
| chr19:2269436-2269697 | Common:3; Rare:117 | ||||
| chr19:2328388-2328710 | Common:2; Rare:139 | ||||
| chr19:2434870-2435005 | Common:5; Rare:71; Clinvar (benign):2 |