| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38831748-38831938 | Common:3; Rare:72; Clinvar (benign):1 | ||||
| chr19:38899572-38899997 | Rare:121 | ||||
| chr19:38930742-38930987 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39390850-39390926 | Rare:32 | ||||
| chr19:39391025-39391424 | Common:1; Rare:160 | ||||
| chr19:39406552-39406852 | Common:1; Rare:76 | ||||
| chr19:39435899-39436176 | Common:5; Rare:106 | ||||
| chr19:39480710-39480912 | Common:3; Rare:110; Clinvar (pathogenic):1 | ||||
| chr19:39498839-39498960 | Common:1; Rare:35 | ||||
| chr19:39846315-39846473 | Common:1; Rare:74 | ||||
| chr19:39970969-39971196 | Common:2; Rare:59 | ||||
| chr19:39996932-39997095 | Common:5; Rare:53 | ||||
| chr19:40056137-40056238 | Rare:14 | ||||
| chr19:40090871-40090959 | Common:1; Rare:26 | ||||
| chr19:40348377-40348739 | Common:4; Rare:121 |