Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:24466335-24466560 | Rare:34 | ||||
chr10:27154315-27154522 | Rare:60 | ||||
chr10:27155161-27155429 | Common:7; Rare:114; Clinvar:5; Clinvar (benign):7 | ||||
chr10:27240466-27240667 | Common:2; Rare:63 | ||||
chr10:27240721-27240902 | Rare:48 | ||||
chr10:27242058-27242235 | Common:1; Rare:76 | ||||
chr10:28532717-28532865 | Common:1; Rare:57 | ||||
chr10:28533002-28533308 | Rare:125 | ||||
chr10:28533325-28533545 | Common:1; Rare:83 | ||||
chr10:29481637-29482024 | Common:2; Rare:78 | ||||
chr10:29486083-29486329 | Rare:69 | ||||
chr10:29736929-29737134 | Common:2; Rare:62 | ||||
chr10:30434044-30434718 | Common:3; Rare:168 | ||||
chr10:31031846-31032028 | Common:1; Rare:70 | ||||
chr10:31032377-31032577 | Common:10; Rare:67 |