Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:43606360-43606482 | Common:3; Rare:40 | ||||
chr10:43648735-43649000 | Common:3; Rare:82 | ||||
chr10:44959624-44959815 | Common:1; Rare:63 | ||||
chr10:45000720-45000968 | Common:1; Rare:104 | ||||
chr10:45727156-45727307 | Common:1; Rare:65 | ||||
chr10:45972355-45972587 | Common:1; Rare:73 | ||||
chr10:46030543-46030768 | Common:1; Rare:71 | ||||
chr10:46911341-46911483 | Rare:11 | ||||
chr10:49762277-49762410 | Common:1; Rare:54 | ||||
chr10:49941908-49942139 | Rare:74 | ||||
chr10:50067786-50068004 | Common:5; Rare:97 | ||||
chr10:50623872-50624079 | Common:1; Rare:82 | ||||
chr10:50624679-50624951 | Common:4; Rare:90 | ||||
chr10:50739905-50739982 | Rare:16 | ||||
chr10:51074402-51074575 | Common:1; Rare:38; Clinvar (benign):2 |