| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7488929-7489202 | Common:2; Rare:128 | ||||
| chr19:7515991-7516113 | Rare:26 | ||||
| chr19:7522370-7522715 | Common:2; Rare:109; Clinvar:2 | ||||
| chr19:7534021-7534246 | Common:4; Rare:63; Clinvar (benign):2 | ||||
| chr19:7535285-7535787 | Common:4; Rare:149; Clinvar:2 | ||||
| chr19:7629474-7629861 | Common:7; Rare:146; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636920-7637226 | Common:4; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:7680686-7680942 | Common:4; Rare:84 | ||||
| chr19:7681768-7681960 | Rare:41 | ||||
| chr19:7699366-7699585 | Common:5; Rare:48 | ||||
| chr19:7701719-7701939 | Common:1; Rare:41 | ||||
| chr19:7702008-7702440 | Common:2; Rare:88 | ||||
| chr19:7903452-7903975 | Common:2; Rare:174 | ||||
| chr19:7920115-7920399 | Rare:102 | ||||
| chr19:7920842-7921049 | Rare:45 |