Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:94895618-94895846 | Common:2; Rare:61 | ||||
chr8:94949362-94949553 | Common:1; Rare:57 | ||||
chr8:95025061-95025203 | Rare:39; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr8:96235514-96235652 | Common:1; Rare:70; Clinvar (benign):2 | ||||
chr8:96261566-96261974 | Common:6; Rare:135 | ||||
chr8:96644969-96645375 | Common:3; Rare:95 | ||||
chr8:98045338-98045675 | Common:3; Rare:100 | ||||
chr8:98117120-98117379 | Common:4; Rare:79 | ||||
chr8:99013007-99013358 | Rare:74; Clinvar:1 | ||||
chr8:100150551-100150709 | Rare:50 | ||||
chr8:100309874-100310305 | Common:1; Rare:156 | ||||
chr8:100950427-100950585 | Common:2; Rare:52 | ||||
chr8:102238738-102239004 | Common:5; Rare:110; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr8:103298730-103298944 | Common:2; Rare:52 | ||||
chr8:103372186-103372547 | Rare:66 |