| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7348759-7348942 | Common:1; Rare:35 | ||||
| chr19:7394963-7395224 | Common:6; Rare:80 | ||||
| chr19:7488933-7489110 | Rare:92 | ||||
| chr19:7516001-7516029 | Rare:5 | ||||
| chr19:7522397-7522726 | Common:2; Rare:108; Clinvar:2 | ||||
| chr19:7534066-7534202 | Common:3; Rare:36; Clinvar (benign):1 | ||||
| chr19:7535311-7535780 | Common:4; Rare:140; Clinvar:2 | ||||
| chr19:7535959-7536003 | Common:3; Rare:15; Clinvar (benign):3 | ||||
| chr19:7629480-7629832 | Common:7; Rare:133; Clinvar (benign):2 | ||||
| chr19:7636959-7637204 | Common:2; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:7680733-7680940 | Common:4; Rare:66 | ||||
| chr19:7681780-7681936 | Rare:29 | ||||
| chr19:7699432-7699735 | Common:8; Rare:64 | ||||
| chr19:7702041-7702434 | Common:2; Rare:81 | ||||
| chr19:7903457-7903976 | Common:2; Rare:172 |