| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7294205-7294646 | Common:7; Rare:104 | ||||
| chr19:7394954-7395248 | Common:6; Rare:83 | ||||
| chr19:7488878-7489240 | Common:3; Rare:153 | ||||
| chr19:7489426-7489683 | Rare:47 | ||||
| chr19:7500791-7500943 | Common:2; Rare:52 | ||||
| chr19:7500996-7501312 | Common:5; Rare:112 | ||||
| chr19:7515895-7516166 | Rare:61 | ||||
| chr19:7522405-7522698 | Common:2; Rare:99; Clinvar:2 | ||||
| chr19:7534021-7534207 | Common:3; Rare:49; Clinvar (benign):1 | ||||
| chr19:7535029-7535146 | Common:1; Rare:29 | ||||
| chr19:7535359-7535747 | Common:4; Rare:110; Clinvar:2 | ||||
| chr19:7595682-7595967 | Common:3; Rare:100 | ||||
| chr19:7596283-7596366 | Rare:20 | ||||
| chr19:7629464-7629886 | Common:7; Rare:156; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636887-7637228 | Common:5; Rare:90; Clinvar:1; Clinvar (benign):1 |