| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4670305-4670547 | Common:5; Rare:94 | ||||
| chr19:4723753-4724067 | Common:6; Rare:119 | ||||
| chr19:4831693-4831763 | Rare:18 | ||||
| chr19:4867621-4867895 | Common:4; Rare:79 | ||||
| chr19:5293179-5293441 | Common:1; Rare:111 | ||||
| chr19:5622725-5623313 | Common:6; Rare:230 | ||||
| chr19:5680484-5680614 | Rare:38 | ||||
| chr19:5680705-5681034 | Rare:78 | ||||
| chr19:5978078-5978393 | Common:3; Rare:117 | ||||
| chr19:6110416-6110834 | Common:2; Rare:124 | ||||
| chr19:6361406-6361667 | Common:1; Rare:83; Clinvar (benign):4 | ||||
| chr19:6393125-6393238 | Common:2; Rare:27 | ||||
| chr19:6697342-6697788 | Common:5; Rare:129; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:6710748-6711065 | Common:3; Rare:95; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:6714171-6714430 | Common:1; Rare:74; Clinvar (benign):2 |