Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:93893867-93893997 | Common:1; Rare:51 | ||||
chr10:94362901-94363006 | Common:2; Rare:43 | ||||
chr10:95561334-95561572 | Common:3; Rare:65 | ||||
chr10:95693915-95694199 | Common:5; Rare:76; Clinvar (benign):1 | ||||
chr10:95907787-95907950 | Common:3; Rare:50 | ||||
chr10:96129999-96130351 | Common:4; Rare:120 | ||||
chr10:96832083-96832299 | Rare:82 | ||||
chr10:97426107-97426310 | Common:2; Rare:95 | ||||
chr10:97445981-97446247 | Rare:69 | ||||
chr10:97633413-97633671 | Common:2; Rare:72 | ||||
chr10:97736939-97737146 | Common:2; Rare:67 | ||||
chr10:98446870-98447029 | Rare:45 | ||||
chr10:99430602-99430930 | Common:3; Rare:75 | ||||
chr10:99659256-99659482 | Common:1; Rare:48 | ||||
chr10:99732074-99732335 | Rare:95; Clinvar:3 |