Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102395609-102395721 | Rare:29 | ||||
chr10:102432556-102432787 | Common:1; Rare:67 | ||||
chr10:102644980-102645163 | Rare:39 | ||||
chr10:102714282-102714638 | Common:2; Rare:120 | ||||
chr10:102776033-102776215 | Common:1; Rare:29 | ||||
chr10:103193243-103193338 | Common:5; Rare:35; Clinvar (benign):1 | ||||
chr10:103396411-103396695 | Rare:101 | ||||
chr10:103451235-103451437 | Rare:43 | ||||
chr10:103452211-103452434 | Rare:67 | ||||
chr10:104121760-104122171 | Common:3; Rare:137 | ||||
chr10:104268956-104269013 | Common:1; Rare:15 | ||||
chr10:109923423-109923615 | Common:1; Rare:66 | ||||
chr10:110007716-110008099 | Common:1; Rare:105 | ||||
chr10:110919263-110919629 | Common:8; Rare:96 | ||||
chr10:112183743-112183844 | Common:2; Rare:41 |