| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6361722-6361867 | Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:6393374-6393580 | Common:2; Rare:60 | ||||
| chr19:6416839-6417071 | Common:1; Rare:80 | ||||
| chr19:6710792-6711065 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:6714171-6714442 | Common:1; Rare:77; Clinvar (benign):2 | ||||
| chr19:6740781-6740939 | Rare:36 | ||||
| chr19:7395022-7395185 | Common:4; Rare:50 | ||||
| chr19:7488997-7489167 | Common:2; Rare:77 | ||||
| chr19:7533848-7534213 | Common:3; Rare:95; Clinvar (benign):1 | ||||
| chr19:7535574-7535785 | Common:3; Rare:77 | ||||
| chr19:7561077-7561237 | Common:3; Rare:42; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:7629503-7629859 | Common:7; Rare:129; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636989-7637143 | Common:2; Rare:51; Clinvar (benign):1 | ||||
| chr19:7920235-7920371 | Rare:62 | ||||
| chr19:7925480-7925771 | Common:2; Rare:75 |