Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:68332882-68333053 | Common:1; Rare:43 | ||||
chr10:70132746-70132915 | Rare:48 | ||||
chr10:70233348-70233563 | Common:5; Rare:75 | ||||
chr10:70888228-70888383 | Common:2; Rare:36 | ||||
chr10:71819465-71819896 | Common:1; Rare:172; Clinvar:5; Clinvar (benign):4 | ||||
chr10:71851187-71851430 | Common:5; Rare:104; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:73110204-73110522 | Rare:57 | ||||
chr10:73167945-73168158 | Rare:57 | ||||
chr10:73495610-73495721 | Rare:21 | ||||
chr10:73641756-73641850 | Rare:11 | ||||
chr10:73744254-73744440 | Common:1; Rare:51 | ||||
chr10:73781939-73782073 | Common:1; Rare:43 | ||||
chr10:73997732-73997892 | Common:1; Rare:31 | ||||
chr10:74150765-74151268 | Common:2; Rare:122 | ||||
chr10:75209884-75210179 | Common:2; Rare:69 |