Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:11012609-11013037 | Rare:62 | ||||
chr10:11193265-11193474 | Rare:41 | ||||
chr10:11255718-11255923 | Common:1; Rare:45 | ||||
chr10:11270127-11270286 | Common:3; Rare:33 | ||||
chr10:13125802-13126030 | Common:2; Rare:65; Clinvar (pathogenic):1 | ||||
chr10:13890799-13891013 | Common:4; Rare:34 | ||||
chr10:14568044-14568119 | Common:3; Rare:15 | ||||
chr10:15718764-15719064 | Common:1; Rare:79 | ||||
chr10:19816795-19816990 | Common:2; Rare:40 | ||||
chr10:19817709-19817982 | Common:2; Rare:59 | ||||
chr10:22251843-22252099 | Rare:54 | ||||
chr10:22253716-22253861 | Common:1; Rare:34 | ||||
chr10:22437823-22438071 | Common:3; Rare:46 | ||||
chr10:23342482-23342891 | Common:1; Rare:76 | ||||
chr10:24118390-24118555 | Rare:39 |