Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:56387423-56387513 | Rare:32 | ||||
chr4:56435546-56435724 | Common:3; Rare:63 | ||||
chr4:56435997-56436307 | Rare:109 | ||||
chr4:56467422-56467679 | Common:2; Rare:97; Clinvar (benign):4 | ||||
chr4:56977597-56977747 | Common:1; Rare:51 | ||||
chr4:67701113-67701358 | Common:4; Rare:117 | ||||
chr4:68349952-68350203 | Rare:93 | ||||
chr4:69495898-69496122 | Common:3; Rare:37 | ||||
chr4:70688427-70688568 | Common:2; Rare:38 | ||||
chr4:70993491-70993649 | Common:4; Rare:48 | ||||
chr4:73869217-73869393 | Common:2; Rare:49 | ||||
chr4:73998665-73998945 | Common:1; Rare:70 | ||||
chr4:74157821-74158150 | Common:2; Rare:133 | ||||
chr4:74444923-74445176 | Common:1; Rare:52 | ||||
chr4:75514273-75514495 | Common:1; Rare:74 |