Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:7069673-7069735 | Common:1; Rare:16 | ||||
chr19:7394964-7395195 | Common:6; Rare:73 | ||||
chr19:7489014-7489184 | Common:2; Rare:75 | ||||
chr19:7533861-7534199 | Common:3; Rare:83; Clinvar (benign):1 | ||||
chr19:7535569-7535766 | Common:3; Rare:71 | ||||
chr19:7629539-7629831 | Common:5; Rare:102; Clinvar (benign):1 | ||||
chr19:7636989-7637176 | Common:2; Rare:56; Clinvar (benign):1 | ||||
chr19:7903542-7903885 | Rare:105 | ||||
chr19:8005513-8005813 | Common:1; Rare:105 | ||||
chr19:8321308-8321497 | Common:2; Rare:83 | ||||
chr19:8390044-8390412 | Common:1; Rare:105 | ||||
chr19:8514121-8514226 | Common:2; Rare:32 | ||||
chr19:9538570-9538771 | Common:1; Rare:63 | ||||
chr19:9621177-9621542 | Common:3; Rare:102 | ||||
chr19:9818806-9818842 | Rare:10 |