Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:22316217-22316536 | Common:3; Rare:143 | ||||
chr10:22321358-22321600 | Rare:86 | ||||
chr10:22325498-22325844 | Common:1; Rare:137 | ||||
chr10:24466335-24466560 | Rare:34 | ||||
chr10:25016291-25016685 | Common:9; Rare:131 | ||||
chr10:25016971-25017110 | Common:4; Rare:64 | ||||
chr10:26697626-26697927 | Common:2; Rare:88; Clinvar:2; Clinvar (benign):3 | ||||
chr10:27100427-27100594 | Common:3; Rare:51; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154310-27154480 | Rare:45 | ||||
chr10:27155161-27155419 | Common:7; Rare:108; Clinvar:5; Clinvar (benign):7 | ||||
chr10:27240372-27240677 | Common:2; Rare:92 | ||||
chr10:27240715-27240940 | Common:1; Rare:58 | ||||
chr10:27242058-27242265 | Common:1; Rare:93 | ||||
chr10:28532515-28532862 | Common:4; Rare:144 | ||||
chr10:28532979-28533191 | Rare:88 |