Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:36288814-36289232 | Common:2; Rare:117; Clinvar:4; Clinvar (benign):5 | ||||
chr22:36331570-36331772 | Common:3; Rare:37 | ||||
chr22:36542194-36542266 | Rare:14 | ||||
chr22:37242493-37242694 | Common:1; Rare:39 | ||||
chr22:37307990-37308056 | Common:1; Rare:15 | ||||
chr22:37354026-37354134 | Common:1; Rare:25 | ||||
chr22:38218691-38218850 | Common:1; Rare:43 | ||||
chr22:38314574-38314689 | Rare:26 | ||||
chr22:39521555-39521797 | Common:1; Rare:120 | ||||
chr22:42777296-42777563 | Common:1; Rare:51 | ||||
chr22:42937552-42937712 | Rare:29 | ||||
chr22:45996650-45996695 | Rare:10 | ||||
chr22:46069052-46069241 | Rare:26 | ||||
chr22:46069832-46070061 | Rare:47 | ||||
chr22:46080057-46080379 | Common:1; Rare:101 |