Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:73252565-73252771 | Common:2; Rare:61; Clinvar:4; Clinvar (benign):2 | ||||
chr10:73495593-73495785 | Rare:47 | ||||
chr10:73495814-73496154 | Common:3; Rare:95 | ||||
chr10:73625955-73626121 | Rare:30 | ||||
chr10:73744008-73744430 | Common:1; Rare:104 | ||||
chr10:73781997-73782088 | Common:1; Rare:30 | ||||
chr10:73997703-73998228 | Common:2; Rare:137; Clinvar (benign):1 | ||||
chr10:73998311-73998354 | Rare:8; Clinvar (benign):1 | ||||
chr10:74151018-74151267 | Common:1; Rare:67 | ||||
chr10:75401743-75401920 | Common:2; Rare:64 | ||||
chr10:77926728-77926936 | Common:1; Rare:70 | ||||
chr10:78029385-78029643 | Common:1; Rare:83; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr10:79347357-79347554 | Common:4; Rare:57 | ||||
chr10:80078653-80078720 | Rare:29 | ||||
chr10:80078994-80079322 | Common:3; Rare:125 |