Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:46184393-46184736 | Common:4; Rare:33 | ||||
chr21:46286237-46286396 | Common:4; Rare:60 | ||||
chr21:46323840-46324202 | Common:2; Rare:126; Clinvar:2; Clinvar (benign):1 | ||||
chr22:17628712-17628848 | Common:1; Rare:43 | ||||
chr22:17638668-17638837 | Rare:59 | ||||
chr22:18077799-18078016 | Common:5; Rare:69; Clinvar:3; Clinvar (benign):2 | ||||
chr22:19291696-19291925 | Common:10; Rare:69 | ||||
chr22:19447690-19447914 | Common:2; Rare:84 | ||||
chr22:19854791-19854977 | Rare:62 | ||||
chr22:19941710-19941886 | Rare:76; Clinvar:6; Clinvar (benign):4 | ||||
chr22:20079936-20080305 | Common:1; Rare:122 | ||||
chr22:20115778-20116187 | Common:1; Rare:138 | ||||
chr22:20319992-20320151 | Common:2; Rare:53 | ||||
chr22:20495776-20495913 | Common:1; Rare:51 | ||||
chr22:20507450-20507622 | Rare:45 |