Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:178615304-178615770 | Common:1; Rare:124; Clinvar:25; Clinvar (benign):8 | ||||
chr2:178621078-178621652 | Common:7; Rare:153; Clinvar:14; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
chr2:178628829-178628971 | Rare:28 | ||||
chr2:178629472-178629743 | Common:1; Rare:58 | ||||
chr2:178629861-178629984 | Rare:16 | ||||
chr2:178632916-178633142 | Rare:78; Clinvar:8; Clinvar (benign):4 | ||||
chr2:178684636-178684951 | Rare:83; Clinvar:10; Clinvar (benign):4 | ||||
chr2:178689066-178689368 | Common:1; Rare:84; Clinvar:8; Clinvar (benign):6 | ||||
chr2:178769678-178770216 | Common:2; Rare:132; Clinvar:13; Clinvar (benign):11 | ||||
chr2:178777418-178777979 | Common:6; Rare:150; Clinvar:27; Clinvar (benign):15 | ||||
chr2:178785613-178785967 | Common:1; Rare:106; Clinvar:22; Clinvar (benign):8 | ||||
chr2:178790621-178790766 | Rare:44; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr2:178791357-178791634 | Rare:45 | ||||
chr2:179049326-179049468 | Rare:34 | ||||
chr2:179058667-179058762 | Common:3; Rare:24 |