Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:55510229-55510464 | Common:3; Rare:49 | ||||
chr16:56404971-56405233 | Common:1; Rare:70 | ||||
chr16:56618683-56618779 | Common:3; Rare:12 | ||||
chr16:56933804-56933831 | Rare:6 | ||||
chr16:57248414-57248584 | Rare:35; Clinvar (pathogenic):1 | ||||
chr16:58511249-58511575 | Common:3; Rare:90 | ||||
chr16:58544532-58544827 | Rare:44 | ||||
chr16:64950591-64950832 | Rare:67 | ||||
chr16:64952931-64953026 | Rare:13 | ||||
chr16:64957008-64957040 | Rare:6 | ||||
chr16:65002745-65002820 | Common:1; Rare:6 | ||||
chr16:65119217-65119277 | Rare:9 | ||||
chr16:65119873-65119997 | Common:1; Rare:22 | ||||
chr16:66617724-66617886 | Rare:28 | ||||
chr16:66723788-66723910 | Common:1; Rare:39 |