Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:32159211-32159397 | Rare:42 | ||||
chr22:32412169-32412345 | Common:2; Rare:53 | ||||
chr22:32474636-32474852 | Common:4; Rare:64; Clinvar:5; Clinvar (benign):2 | ||||
chr22:35257394-35257541 | Common:1; Rare:46 | ||||
chr22:35299635-35299935 | Common:3; Rare:80 | ||||
chr22:35399910-35400158 | Rare:85 | ||||
chr22:35839865-35840009 | Rare:22 | ||||
chr22:35840190-35840673 | Common:3; Rare:110 | ||||
chr22:35961466-35961724 | Rare:54 | ||||
chr22:36387935-36388414 | Common:5; Rare:135; Clinvar:2; Clinvar (benign):1 | ||||
chr22:36481277-36481763 | Common:5; Rare:124 | ||||
chr22:36482010-36482241 | Common:1; Rare:57 | ||||
chr22:36506787-36507179 | Common:5; Rare:118 | ||||
chr22:36529080-36529578 | Common:8; Rare:157 | ||||
chr22:36703464-36703540 | Common:1; Rare:22 |