Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:92848322-92848531 | Rare:79 | ||||
chr10:93702505-93702699 | Common:3; Rare:69 | ||||
chr10:93757635-93758039 | Common:1; Rare:68; Clinvar:3; Clinvar (benign):1 | ||||
chr10:94362901-94363048 | Common:2; Rare:61 | ||||
chr10:95194174-95194239 | Rare:8 | ||||
chr10:95693891-95694182 | Common:5; Rare:93; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr10:95907781-95907946 | Common:2; Rare:53 | ||||
chr10:97425885-97426302 | Common:15; Rare:202 | ||||
chr10:97445963-97446171 | Common:1; Rare:58 | ||||
chr10:97498387-97498544 | Common:2; Rare:62 | ||||
chr10:97633431-97633594 | Common:2; Rare:37 | ||||
chr10:97736939-97737195 | Common:2; Rare:86 | ||||
chr10:98446886-98447008 | Rare:35 | ||||
chr10:99430602-99430936 | Common:3; Rare:77 | ||||
chr10:99659258-99659536 | Common:1; Rare:68 |