Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:74150771-74151271 | Common:2; Rare:123 | ||||
chr10:74176411-74176715 | Rare:75; Clinvar:1 | ||||
chr10:74176732-74176840 | Rare:32; Clinvar:2 | ||||
chr10:75109081-75109331 | Common:1; Rare:58 | ||||
chr10:75111558-75111729 | Rare:50 | ||||
chr10:75210459-75210900 | Common:2; Rare:150 | ||||
chr10:75210920-75211026 | Rare:35 | ||||
chr10:75401339-75401423 | Common:5; Rare:46 | ||||
chr10:75431563-75431695 | Common:2; Rare:45 | ||||
chr10:77925850-77926144 | Common:3; Rare:55 | ||||
chr10:78029447-78029646 | Common:1; Rare:62; Clinvar (benign):1 | ||||
chr10:78033564-78033904 | Common:2; Rare:106; Clinvar (benign):4 | ||||
chr10:79276902-79277201 | Common:4; Rare:73 | ||||
chr10:79982047-79982371 | Common:4; Rare:68 | ||||
chr10:80078600-80078708 | Rare:42 |