Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:52659194-52659420 | Common:1; Rare:77 | ||||
chr4:55546798-55547162 | Common:2; Rare:131 | ||||
chr4:55853469-55853743 | Rare:73 | ||||
chr4:56387417-56387528 | Rare:35 | ||||
chr4:56435467-56435973 | Common:6; Rare:166 | ||||
chr4:56467530-56467655 | Common:1; Rare:50; Clinvar (benign):1 | ||||
chr4:56977574-56977745 | Common:1; Rare:67 | ||||
chr4:57110383-57110530 | Common:1; Rare:48 | ||||
chr4:67701115-67701371 | Common:4; Rare:121 | ||||
chr4:70688226-70688586 | Common:2; Rare:94 | ||||
chr4:70902221-70902459 | Common:5; Rare:79 | ||||
chr4:70993492-70993658 | Common:4; Rare:51 | ||||
chr4:73258505-73258905 | Common:1; Rare:118 | ||||
chr4:73259129-73259163 | Rare:6 | ||||
chr4:74099145-74099455 | Common:3; Rare:74 |