Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:41327775-41328029 | Common:2; Rare:55 | ||||
chr4:44316677-44316909 | Common:3; Rare:44 | ||||
chr4:44879839-44880028 | Common:4; Rare:44 | ||||
chr4:52657906-52658151 | Common:1; Rare:47 | ||||
chr4:52712213-52712523 | Common:4; Rare:81 | ||||
chr4:52713716-52714111 | Common:1; Rare:70 | ||||
chr4:52741831-52742090 | Rare:48 | ||||
chr4:52863000-52863275 | Common:1; Rare:64 | ||||
chr4:53007139-53007183 | Rare:6 | ||||
chr4:53461443-53461742 | Rare:88 | ||||
chr4:53476922-53477145 | Rare:43 | ||||
chr4:55456271-55456557 | Rare:50 | ||||
chr4:56410277-56410535 | Common:2; Rare:53 | ||||
chr4:56490331-56490646 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):3 | ||||
chr4:56874316-56874482 | Common:3; Rare:34 |