Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:145482859-145483001 | Rare:21 | ||||
chr4:145619264-145619396 | Rare:55 | ||||
chr4:146521859-146521974 | Rare:23 | ||||
chr4:147617217-147617455 | Common:1; Rare:56 | ||||
chr4:147684106-147684265 | Common:1; Rare:60 | ||||
chr4:148442375-148442712 | Rare:99; Clinvar:4; Clinvar (benign):2 | ||||
chr4:151408874-151409217 | Common:5; Rare:111 | ||||
chr4:152779864-152780055 | Common:1; Rare:51 | ||||
chr4:156971123-156971189 | Rare:9 | ||||
chr4:158671830-158672313 | Common:5; Rare:121; Clinvar:2; Clinvar (benign):1 | ||||
chr4:158723327-158723538 | Common:2; Rare:91 | ||||
chr4:165112820-165113014 | Common:1; Rare:57 | ||||
chr4:165327412-165327734 | Common:2; Rare:93 | ||||
chr4:168480458-168480510 | Rare:12 | ||||
chr4:169010223-169010456 | Common:1; Rare:69 |