| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37779520-37779693 | Common:1; Rare:34 | ||||
| chr19:37817248-37817520 | Common:2; Rare:52 | ||||
| chr19:38315898-38316152 | Common:1; Rare:73 | ||||
| chr19:38336321-38336472 | Common:1; Rare:32 | ||||
| chr19:38374407-38374800 | Rare:143 | ||||
| chr19:38618832-38619134 | Common:3; Rare:87 | ||||
| chr19:38831726-38832050 | Common:4; Rare:108; Clinvar (benign):1 | ||||
| chr19:38852324-38852569 | Rare:56 | ||||
| chr19:38899513-38900026 | Rare:154 | ||||
| chr19:38930726-38931013 | Common:3; Rare:82; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39390991-39391515 | Common:1; Rare:202 | ||||
| chr19:39406689-39406925 | Rare:91 | ||||
| chr19:39435846-39436143 | Common:6; Rare:110 | ||||
| chr19:39480725-39480912 | Common:3; Rare:103; Clinvar (pathogenic):1 | ||||
| chr19:39846307-39846499 | Common:1; Rare:93 |