Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:1417178-1417443 | Common:1; Rare:61 | ||||
chr19:1417985-1418337 | Common:2; Rare:90 | ||||
chr19:1876164-1876283 | Common:1; Rare:43 | ||||
chr19:3361167-3361205 | Rare:9 | ||||
chr19:3409570-3409764 | Rare:50 | ||||
chr19:3670254-3670395 | Rare:37 | ||||
chr19:6066949-6067078 | Rare:24 | ||||
chr19:6109021-6109111 | Common:1; Rare:19 | ||||
chr19:6707092-6707437 | Common:2; Rare:112; Clinvar:1; Clinvar (benign):4 | ||||
chr19:6717636-6718413 | Common:9; Rare:192; Clinvar:2; Clinvar (benign):1 | ||||
chr19:7183122-7183343 | Common:2; Rare:39 | ||||
chr19:7197179-7197316 | Common:1; Rare:35 | ||||
chr19:7198030-7198338 | Common:5; Rare:106 | ||||
chr19:7203091-7203372 | Rare:39 | ||||
chr19:7211766-7211856 | Common:3; Rare:19 |