Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:248825857-248826025 | Common:3; Rare:50 | ||||
chr1:248826298-248826354 | Rare:18 | ||||
chr1:248838040-248838489 | Common:3; Rare:140 | ||||
chr1:248838760-248838791 | Rare:7 | ||||
chr1:248858899-248859175 | Rare:102 | ||||
chr10:134554-134829 | Rare:66 | ||||
chr10:649953-650277 | Common:1; Rare:97 | ||||
chr10:650342-650369 | Rare:5 | ||||
chr10:931680-932007 | Rare:110 | ||||
chr10:988320-988518 | Common:1; Rare:88 | ||||
chr10:1048865-1049099 | Common:2; Rare:119 | ||||
chr10:1049314-1049527 | Common:6; Rare:89 | ||||
chr10:1056702-1056872 | Common:3; Rare:63 | ||||
chr10:3138998-3139262 | Common:2; Rare:82 | ||||
chr10:3145596-3145913 | Common:4; Rare:88; Clinvar (benign):1 |