| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39385194-39385321 | Rare:23 | ||||
| chr19:39386766-39386922 | Rare:39 | ||||
| chr19:39390840-39391471 | Common:1; Rare:238 | ||||
| chr19:39406710-39406946 | Rare:99 | ||||
| chr19:39407104-39407106 | |||||
| chr19:39435846-39436163 | Common:6; Rare:116 | ||||
| chr19:39445474-39445829 | Common:2; Rare:96 | ||||
| chr19:39846294-39846468 | Common:1; Rare:79 | ||||
| chr19:39970957-39971223 | Common:3; Rare:73 | ||||
| chr19:39996944-39997101 | Common:5; Rare:52 | ||||
| chr19:40090316-40090422 | Rare:32 | ||||
| chr19:40090865-40090984 | Common:1; Rare:35 | ||||
| chr19:40348343-40348739 | Common:4; Rare:128 | ||||
| chr19:40377824-40378117 | Common:2; Rare:104; Clinvar (benign):1 | ||||
| chr19:40444249-40444518 | Common:3; Rare:86 |