Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:97663993-97664395 | Rare:108 | ||||
chr2:98608416-98608640 | Common:1; Rare:96; Clinvar (benign):1 | ||||
chr2:99154883-99155048 | Common:1; Rare:68; Clinvar (benign):2 | ||||
chr2:99180984-99181226 | Common:2; Rare:71 | ||||
chr2:101252846-101252952 | Rare:28 | ||||
chr2:101474693-101474812 | Common:1; Rare:18 | ||||
chr2:105337225-105337569 | Common:5; Rare:113 | ||||
chr2:108449126-108449230 | Rare:31 | ||||
chr2:108534158-108534475 | Common:7; Rare:129 | ||||
chr2:109614059-109614370 | Common:4; Rare:115 | ||||
chr2:112645696-112645942 | Common:1; Rare:88 | ||||
chr2:113627078-113627303 | Common:3; Rare:64 | ||||
chr2:113756483-113756732 | Common:2; Rare:74 | ||||
chr2:113889709-113890318 | Common:9; Rare:191 | ||||
chr2:119366794-119367059 | Common:1; Rare:78 |