| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4723755-4724064 | Common:6; Rare:115 | ||||
| chr19:4831663-4831765 | Rare:32 | ||||
| chr19:4867619-4867855 | Common:3; Rare:71 | ||||
| chr19:5293213-5293425 | Common:1; Rare:95 | ||||
| chr19:5622725-5623181 | Common:5; Rare:177 | ||||
| chr19:5680474-5681169 | Rare:206 | ||||
| chr19:5720135-5720347 | Rare:79 | ||||
| chr19:5791160-5791343 | Common:4; Rare:56 | ||||
| chr19:5978078-5978383 | Common:3; Rare:113 | ||||
| chr19:6393125-6393222 | Common:2; Rare:21 | ||||
| chr19:6710814-6711065 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:6740669-6740939 | Common:1; Rare:61 | ||||
| chr19:7395022-7395185 | Common:4; Rare:50 | ||||
| chr19:7535543-7535769 | Common:3; Rare:81; Clinvar:2 | ||||
| chr19:7629531-7629844 | Common:5; Rare:111; Clinvar (benign):2; Clinvar (pathogenic):1 |