Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102055882-102056045 | Common:1; Rare:46 | ||||
chr10:102056071-102056413 | Common:3; Rare:81 | ||||
chr10:102064968-102065031 | Rare:9 | ||||
chr10:102065122-102065687 | Common:3; Rare:198; Clinvar:1; Clinvar (benign):2 | ||||
chr10:102065716-102066105 | Common:5; Rare:129; Clinvar:2; Clinvar (benign):5 | ||||
chr10:102114341-102114516 | Common:1; Rare:43 | ||||
chr10:102114518-102114581 | Rare:22 | ||||
chr10:102114727-102115149 | Common:3; Rare:121 | ||||
chr10:102120204-102120732 | Common:3; Rare:170 | ||||
chr10:102120750-102120866 | Rare:34 | ||||
chr10:102132570-102132717 | Rare:34 | ||||
chr10:102132860-102133354 | Common:1; Rare:142 | ||||
chr10:102152006-102152277 | Common:3; Rare:60 | ||||
chr10:102152320-102152614 | Common:1; Rare:129 | ||||
chr10:102152742-102152867 | Rare:24 |