Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:27240396-27240667 | Common:2; Rare:86 | ||||
chr10:27240741-27240892 | Rare:41 | ||||
chr10:27242058-27242226 | Common:1; Rare:73 | ||||
chr10:27504031-27504356 | Rare:149; Clinvar:4; Clinvar (benign):1 | ||||
chr10:28532714-28532880 | Common:1; Rare:60 | ||||
chr10:28533026-28533582 | Common:1; Rare:226 | ||||
chr10:29634899-29635038 | Rare:34 | ||||
chr10:29735373-29735711 | Common:4; Rare:101 | ||||
chr10:29735754-29735976 | Common:3; Rare:43 | ||||
chr10:29736880-29737105 | Common:2; Rare:65 | ||||
chr10:30434056-30434214 | Common:1; Rare:34 | ||||
chr10:30434551-30434693 | Common:1; Rare:40 | ||||
chr10:31031822-31032018 | Common:1; Rare:69 | ||||
chr10:31319031-31319289 | Common:2; Rare:74 | ||||
chr10:31928717-31928940 | Common:3; Rare:89 |