| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry | 
|---|---|---|---|---|---|
| chr19:38831769-38832061 | Common:4; Rare:83; Clinvar (benign):1 | ||||
| chr19:38852318-38852434 | Rare:33 | ||||
| chr19:38899586-38900018 | Rare:127 | ||||
| chr19:38930722-38930987 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39390991-39391431 | Common:1; Rare:169 | ||||
| chr19:39406710-39406852 | Rare:55 | ||||
| chr19:39970948-39971203 | Common:3; Rare:70 | ||||
| chr19:40090923-40090974 | Rare:13 | ||||
| chr19:40348399-40348724 | Common:4; Rare:104 | ||||
| chr19:40465693-40466098 | Common:3; Rare:127 | ||||
| chr19:41218963-41219238 | Common:2; Rare:51 | ||||
| chr19:41264985-41265133 | Common:1; Rare:32 | ||||
| chr19:42220128-42220341 | Common:2; Rare:60 | ||||
| chr19:43527183-43527308 | Common:4; Rare:49; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr19:43901770-43901882 | Rare:24 |