Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:86968193-86968501 | Common:5; Rare:69 | ||||
chr10:87094939-87095206 | Common:1; Rare:63; Clinvar:2 | ||||
chr10:87504808-87504907 | Common:1; Rare:38 | ||||
chr10:87818158-87818324 | Rare:63 | ||||
chr10:89414673-89414778 | Common:2; Rare:48 | ||||
chr10:89701424-89701617 | Common:1; Rare:51 | ||||
chr10:91163008-91163073 | Rare:15 | ||||
chr10:92291022-92291344 | Common:5; Rare:104 | ||||
chr10:92574018-92574137 | Common:1; Rare:35 | ||||
chr10:93757685-93757982 | Common:1; Rare:55; Clinvar:3; Clinvar (benign):1 | ||||
chr10:95907884-95907927 | Common:1; Rare:13 | ||||
chr10:96832025-96832295 | Rare:104 | ||||
chr10:97426061-97426298 | Common:2; Rare:100 | ||||
chr10:97445983-97446217 | Rare:60 | ||||
chr10:99430631-99430930 | Common:3; Rare:66 |