Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:93740944-93741167 | Rare:75 | ||||
chr8:93916677-93917003 | Common:3; Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
chr8:94553445-94553763 | Common:3; Rare:112 | ||||
chr8:94895679-94895802 | Rare:39 | ||||
chr8:94949350-94949549 | Common:1; Rare:61 | ||||
chr8:95269387-95269704 | Common:6; Rare:118 | ||||
chr8:96235514-96235661 | Common:1; Rare:75; Clinvar (benign):2 | ||||
chr8:96261544-96261997 | Common:6; Rare:152 | ||||
chr8:96493743-96494114 | Common:1; Rare:103 | ||||
chr8:97868894-97869158 | Common:2; Rare:54 | ||||
chr8:98045338-98045679 | Common:4; Rare:102 | ||||
chr8:98117108-98117325 | Common:2; Rare:78 | ||||
chr8:99013007-99013383 | Rare:78; Clinvar:1 | ||||
chr8:100150564-100150708 | Rare:44 | ||||
chr8:100309904-100310296 | Common:1; Rare:142 |