Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:87342318-87342425 | Common:2; Rare:33 | ||||
chr10:87862245-87862570 | Rare:158; Clinvar:1 | ||||
chr10:88939620-88939909 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
chr10:88948800-88949117 | Rare:61; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr10:88951586-88952015 | Common:1; Rare:88 | ||||
chr10:91807491-91807717 | Rare:45 | ||||
chr10:92591651-92591795 | Rare:44 | ||||
chr10:95231105-95231207 | Rare:21 | ||||
chr10:95476462-95476775 | Common:1; Rare:47 | ||||
chr10:95503051-95503212 | Rare:17 | ||||
chr10:96089853-96089943 | Rare:20 | ||||
chr10:96090198-96090354 | Common:3; Rare:69 | ||||
chr10:97432062-97432425 | Common:1; Rare:76 | ||||
chr10:100373311-100373538 | Common:1; Rare:46 | ||||
chr10:102449736-102449845 | Common:1; Rare:25 |