| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:5680473-5680673 | Rare:70 | ||||
| chr19:5680705-5681040 | Rare:79 | ||||
| chr19:5978078-5978408 | Common:3; Rare:124 | ||||
| chr19:6110416-6110846 | Common:2; Rare:129 | ||||
| chr19:6381123-6381382 | Common:3; Rare:102 | ||||
| chr19:6416839-6417019 | Common:1; Rare:66 | ||||
| chr19:6684773-6685155 | Rare:100; Clinvar (benign):1 | ||||
| chr19:6710643-6711081 | Common:3; Rare:134; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:6714164-6714442 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:6737212-6737313 | Common:1; Rare:31 | ||||
| chr19:6740627-6741104 | Common:1; Rare:122 | ||||
| chr19:7395022-7395185 | Common:4; Rare:50 | ||||
| chr19:7488988-7489087 | Rare:46 | ||||
| chr19:7535574-7535807 | Common:3; Rare:86 | ||||
| chr19:7629491-7629867 | Common:7; Rare:141; Clinvar (benign):2; Clinvar (pathogenic):1 |