Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102714197-102714660 | Common:2; Rare:151 | ||||
chr10:102776057-102776228 | Common:1; Rare:26 | ||||
chr10:103193248-103193392 | Common:5; Rare:45; Clinvar (benign):1 | ||||
chr10:103396417-103396702 | Rare:103 | ||||
chr10:103918205-103918540 | Common:2; Rare:82 | ||||
chr10:104353565-104353787 | Common:2; Rare:58 | ||||
chr10:110007673-110008019 | Rare:105 | ||||
chr10:110304961-110305049 | Rare:24 | ||||
chr10:110871622-110871964 | Rare:111 | ||||
chr10:110919285-110919632 | Common:7; Rare:92 | ||||
chr10:112183739-112183821 | Common:2; Rare:32 | ||||
chr10:112446742-112447294 | Common:3; Rare:132 | ||||
chr10:113854392-113854428 | Rare:5 | ||||
chr10:113854591-113854874 | Common:1; Rare:70 | ||||
chr10:118046686-118047022 | Common:4; Rare:109 |