Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:29634862-29635085 | Rare:49 | ||||
chr10:29635282-29635524 | Rare:41 | ||||
chr10:29735369-29736104 | Common:7; Rare:191 | ||||
chr10:29736906-29737084 | Common:1; Rare:59 | ||||
chr10:30059522-30059654 | Common:1; Rare:54 | ||||
chr10:30348514-30348563 | Rare:9 | ||||
chr10:30348575-30348660 | Rare:7 | ||||
chr10:30348788-30348938 | Rare:29 | ||||
chr10:30348966-30349142 | Common:2; Rare:55; Clinvar (benign):1 | ||||
chr10:30349188-30349446 | Common:12; Rare:112 | ||||
chr10:30433368-30433449 | Rare:29 | ||||
chr10:30433451-30434086 | Common:4; Rare:182 | ||||
chr10:30434087-30434248 | Common:1; Rare:40 | ||||
chr10:30434506-30434728 | Common:2; Rare:61 | ||||
chr10:30434877-30435061 | Common:2; Rare:37 |