Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:77889528-77889661 | Rare:17 | ||||
chr10:77925922-77926109 | Common:3; Rare:38 | ||||
chr10:77926205-77926353 | Rare:42 | ||||
chr10:77926728-77926940 | Common:1; Rare:70 | ||||
chr10:78029368-78029643 | Common:1; Rare:89; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr10:78033634-78033914 | Common:2; Rare:93; Clinvar (benign):4 | ||||
chr10:78035347-78035592 | Rare:67; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr10:79068749-79069020 | Common:2; Rare:84 | ||||
chr10:80078595-80078708 | Rare:43 | ||||
chr10:80078896-80079302 | Common:5; Rare:141 | ||||
chr10:80289632-80289983 | Common:1; Rare:54 | ||||
chr10:80408425-80408727 | Common:1; Rare:84 | ||||
chr10:80453981-80454379 | Common:3; Rare:133 | ||||
chr10:84139281-84139604 | Common:4; Rare:86 | ||||
chr10:84194435-84194668 | Common:1; Rare:67 |