Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:43734774-43735062 | Rare:56 | ||||
chr21:44323644-44323898 | Common:2; Rare:84; Clinvar:1 | ||||
chr21:45496920-45497049 | Rare:42; Clinvar:1 | ||||
chr21:45989313-45989608 | Common:4; Rare:71; Clinvar (benign):3 | ||||
chr21:45989985-45990204 | Common:4; Rare:80 | ||||
chr22:19142584-19142727 | Rare:63 | ||||
chr22:19171637-19171724 | Rare:28 | ||||
chr22:20126058-20126350 | Common:2; Rare:74 | ||||
chr22:20130994-20131285 | Common:5; Rare:101 | ||||
chr22:20141782-20142063 | Common:2; Rare:52 | ||||
chr22:22298040-22298206 | Common:2; Rare:73 | ||||
chr22:24221803-24222032 | Common:2; Rare:41 | ||||
chr22:25447990-25448131 | Common:3; Rare:46 | ||||
chr22:28116663-28116778 | Rare:16 | ||||
chr22:30969061-30969278 | Common:2; Rare:62 |