Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:50622283-50622473 | Common:1; Rare:47 | ||||
chr10:50622945-50623165 | Common:2; Rare:57 | ||||
chr10:50623360-50623466 | Common:1; Rare:22 | ||||
chr10:51467816-51468077 | Rare:62; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr10:51698279-51698461 | Common:2; Rare:50 | ||||
chr10:52755409-52755747 | Common:3; Rare:58 | ||||
chr10:61903128-61903363 | Common:1; Rare:68 | ||||
chr10:61939589-61939876 | Common:1; Rare:43 | ||||
chr10:61942832-61943047 | Common:1; Rare:41 | ||||
chr10:62051091-62051150 | Rare:9 | ||||
chr10:62051164-62051293 | Rare:27 | ||||
chr10:62056639-62056931 | Common:2; Rare:45 | ||||
chr10:62058966-62059252 | Common:1; Rare:39 | ||||
chr10:62064197-62064390 | Rare:24 | ||||
chr10:63265158-63265323 | Rare:33 |