Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:57185979-57186333 | Common:1; Rare:100 | ||||
chr16:57244971-57245357 | Common:3; Rare:130 | ||||
chr16:57447354-57447484 | Common:2; Rare:35; Clinvar:2 | ||||
chr16:57999560-57999664 | Rare:22 | ||||
chr16:58001302-58001466 | Rare:48 | ||||
chr16:58116041-58116245 | Common:1; Rare:46 | ||||
chr16:58629783-58630159 | Common:2; Rare:100 | ||||
chr16:66516810-66517163 | Rare:61; Clinvar (pathogenic):1 | ||||
chr16:66552476-66552660 | Rare:77 | ||||
chr16:66934377-66934528 | Rare:56 | ||||
chr16:67226800-67227151 | Common:2; Rare:121 | ||||
chr16:67247437-67247710 | Rare:91 | ||||
chr16:67393423-67393670 | Common:1; Rare:60 | ||||
chr16:67481084-67481404 | Common:1; Rare:121 | ||||
chr16:67531387-67531587 | Rare:30 |