Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:95907806-95907923 | Common:1; Rare:34 | ||||
chr10:96129938-96130063 | Common:1; Rare:49 | ||||
chr10:97426040-97426300 | Common:2; Rare:115 | ||||
chr10:97445975-97446239 | Rare:69 | ||||
chr10:97498364-97498550 | Common:2; Rare:83 | ||||
chr10:97498694-97498947 | Common:2; Rare:73 | ||||
chr10:97633446-97633637 | Common:2; Rare:51 | ||||
chr10:98134537-98134688 | Common:1; Rare:54 | ||||
chr10:99430622-99430919 | Common:3; Rare:68 | ||||
chr10:99659245-99659562 | Common:1; Rare:80 | ||||
chr10:99732070-99732331 | Rare:97; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100185918-100186157 | Rare:88 | ||||
chr10:100267606-100267753 | Common:3; Rare:46 | ||||
chr10:100286605-100286751 | Common:5; Rare:82 | ||||
chr10:100347058-100347458 | Common:3; Rare:100 |