Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:68331910-68332276 | Common:2; Rare:126 | ||||
chr10:68332689-68332731 | Rare:13 | ||||
chr10:68332837-68333308 | Common:2; Rare:106 | ||||
chr10:68336178-68336397 | Rare:51 | ||||
chr10:68336720-68337052 | Common:2; Rare:61 | ||||
chr10:68407181-68407440 | Common:5; Rare:88 | ||||
chr10:68471927-68472014 | Common:1; Rare:49 | ||||
chr10:68527412-68527823 | Common:3; Rare:124 | ||||
chr10:68755515-68755718 | Rare:50 | ||||
chr10:68956070-68956308 | Common:2; Rare:82 | ||||
chr10:68988571-68989117 | Common:4; Rare:147; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr10:69179940-69180350 | Common:3; Rare:140 | ||||
chr10:69801757-69802010 | Common:1; Rare:64 | ||||
chr10:69802430-69802614 | Rare:57 | ||||
chr10:70132740-70132939 | Common:1; Rare:54 |