Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:52791597-52791757 | Common:1; Rare:69 | ||||
chr14:52951003-52951405 | Common:4; Rare:142 | ||||
chr14:53152371-53152539 | Rare:64; Clinvar (benign):1 | ||||
chr14:53153240-53153481 | Common:3; Rare:97 | ||||
chr14:53956823-53956986 | Rare:40 | ||||
chr14:54441451-54441766 | Common:1; Rare:64 | ||||
chr14:54488923-54489212 | Common:2; Rare:76 | ||||
chr14:54509623-54509959 | Common:6; Rare:121 | ||||
chr14:54566990-54567177 | Rare:48 | ||||
chr14:54902819-54902976 | Rare:44; Clinvar (benign):1 | ||||
chr14:55027046-55027326 | Common:2; Rare:77 | ||||
chr14:55051462-55051749 | Rare:125 | ||||
chr14:55191518-55191834 | Common:7; Rare:86 | ||||
chr14:55271300-55271473 | Common:1; Rare:68 | ||||
chr14:55272009-55272039 | Common:1; Rare:7 |