| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4182495-4182692 | Common:1; Rare:76; Clinvar:1 | ||||
| chr19:4279092-4279269 | Rare:40 | ||||
| chr19:4457716-4457997 | Common:13; Rare:103 | ||||
| chr19:4723741-4723846 | Common:1; Rare:35 | ||||
| chr19:4791424-4791750 | Common:1; Rare:97 | ||||
| chr19:5293211-5293461 | Common:1; Rare:107 | ||||
| chr19:5622701-5623367 | Common:6; Rare:260 | ||||
| chr19:5680473-5681039 | Rare:157 | ||||
| chr19:5978062-5978406 | Common:3; Rare:130 | ||||
| chr19:6710643-6711065 | Common:3; Rare:128; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:7395033-7395203 | Common:4; Rare:55 | ||||
| chr19:7489008-7489103 | Rare:44 | ||||
| chr19:7535570-7535791 | Common:3; Rare:81 | ||||
| chr19:7629520-7629844 | Common:5; Rare:117; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636953-7637143 | Common:2; Rare:59; Clinvar (benign):1 |