Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:5978083-5978383 | Common:3; Rare:112 | ||||
chr19:7629543-7629820 | Common:5; Rare:97; Clinvar (benign):1 | ||||
chr19:8321345-8321497 | Common:2; Rare:62 | ||||
chr19:8390062-8390416 | Common:1; Rare:100 | ||||
chr19:10928594-10928818 | Common:2; Rare:66 | ||||
chr19:11197508-11197625 | Common:1; Rare:31 | ||||
chr19:14529272-14529631 | Common:1; Rare:147 | ||||
chr19:17405587-17405741 | Common:1; Rare:28 | ||||
chr19:18919346-18919743 | Common:2; Rare:140 | ||||
chr19:19033494-19033610 | Common:1; Rare:38 | ||||
chr19:19192111-19192208 | Common:1; Rare:34 | ||||
chr19:29213135-29213219 | Common:1; Rare:34 | ||||
chr19:29665253-29665484 | Common:4; Rare:84 | ||||
chr19:35745383-35745651 | Rare:87 | ||||
chr19:36573276-36573384 | Common:3; Rare:20 |