Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:41468949-41469142 | Rare:54 | ||||
chr22:41621018-41621380 | Common:7; Rare:133 | ||||
chr22:42090745-42091047 | Common:1; Rare:100 | ||||
chr22:42614901-42615244 | Common:3; Rare:132 | ||||
chr22:42649316-42649591 | Common:6; Rare:97 | ||||
chr22:46053777-46053864 | Rare:33 | ||||
chr22:46250245-46250396 | Common:2; Rare:43 | ||||
chr22:46296745-46296915 | Rare:56 | ||||
chr22:46762526-46762693 | Common:3; Rare:58 | ||||
chr22:49918312-49918712 | Common:4; Rare:143; Clinvar (benign):3 | ||||
chr22:50525539-50525738 | Common:4; Rare:109; Clinvar:3; Clinvar (benign):1 | ||||
chr22:50582788-50583124 | Common:7; Rare:104; Clinvar:2; Clinvar (benign):3 | ||||
chr22:50628034-50628306 | Common:9; Rare:120; Clinvar:3; Clinvar (benign):1 | ||||
chr22:50783606-50783822 | Common:2; Rare:66 | ||||
chr3:9792414-9792543 | Rare:34 |