Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:30922226-30922339 | Rare:51 | ||||
chr22:30969044-30969292 | Common:2; Rare:70 | ||||
chr22:31126302-31127037 | Common:5; Rare:251 | ||||
chr22:31133201-31133494 | Common:2; Rare:73 | ||||
chr22:31291285-31291332 | Common:1; Rare:18 | ||||
chr22:32804126-32804199 | Rare:16 | ||||
chr22:32808662-32808794 | Common:1; Rare:24 | ||||
chr22:32857000-32857366 | Common:3; Rare:72; Clinvar:2; Clinvar (benign):2 | ||||
chr22:35838681-35838741 | Rare:10 | ||||
chr22:36288725-36289301 | Common:2; Rare:174; Clinvar:6; Clinvar (benign):10 | ||||
chr22:36320853-36321046 | Rare:37 | ||||
chr22:36331576-36331738 | Common:2; Rare:28 | ||||
chr22:37607211-37607323 | Common:1; Rare:29 | ||||
chr22:37631947-37632055 | Common:1; Rare:34 | ||||
chr22:38176171-38176231 | Rare:10 |