Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:124092711-124092853 | Rare:36 | ||||
chr10:124403510-124403746 | Common:1; Rare:65 | ||||
chr10:124418882-124419093 | Common:4; Rare:98; Clinvar:3; Clinvar (benign):1 | ||||
chr10:124461690-124461888 | Common:5; Rare:69 | ||||
chr10:124461988-124462162 | Common:3; Rare:59 | ||||
chr10:124744054-124744609 | Common:2; Rare:196 | ||||
chr10:124791397-124791464 | Common:1; Rare:16 | ||||
chr10:124791481-124791505 | Rare:4 | ||||
chr10:124791732-124792049 | Common:3; Rare:155 | ||||
chr10:124792179-124792256 | Rare:18 | ||||
chr10:124801611-124801911 | Rare:100 | ||||
chr10:125719385-125719833 | Common:1; Rare:167 | ||||
chr10:125823157-125823605 | Common:2; Rare:161; Clinvar:1; Clinvar (benign):2 | ||||
chr10:125896400-125896514 | Common:2; Rare:4 | ||||
chr10:128047374-128047692 | Common:4; Rare:109 |