Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:47553478-47553541 | Rare:3 | ||||
chr10:47705934-47706064 | Common:3; Rare:30 | ||||
chr10:50622174-50622446 | Common:2; Rare:60 | ||||
chr10:61903108-61903357 | Common:1; Rare:71 | ||||
chr10:71965187-71965347 | Rare:35 | ||||
chr10:72340792-72341137 | Common:3; Rare:110 | ||||
chr10:73126205-73126240 | Rare:8 | ||||
chr10:73247242-73247362 | Rare:62 | ||||
chr10:73730456-73730595 | Common:1; Rare:37 | ||||
chr10:74111750-74112059 | Common:2; Rare:92; Clinvar:9; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
chr10:74117731-74118277 | Common:2; Rare:97; Clinvar:3; Clinvar (benign):4 | ||||
chr10:75403347-75403568 | Common:1; Rare:46 | ||||
chr10:77925477-77925702 | Rare:38 | ||||
chr10:79826320-79826901 | Common:5; Rare:175 | ||||
chr10:86666617-86666826 | Rare:52 |