Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:118836025-118836299 | Common:3; Rare:58 | ||||
chr4:119212355-119212777 | Common:5; Rare:131 | ||||
chr4:119213071-119213367 | Rare:49 | ||||
chr4:119627610-119627788 | Rare:27 | ||||
chr4:119627980-119628099 | Common:1; Rare:28 | ||||
chr4:119628557-119628973 | Common:4; Rare:169 | ||||
chr4:120066748-120066927 | Common:2; Rare:58 | ||||
chr4:120922706-120922905 | Rare:61; Clinvar:4 | ||||
chr4:121696701-121697063 | Common:5; Rare:88 | ||||
chr4:122732445-122732734 | Common:1; Rare:86; Clinvar (benign):1 | ||||
chr4:122922901-122923139 | Common:2; Rare:68 | ||||
chr4:127880775-127880939 | Rare:56 | ||||
chr4:128287445-128287572 | Common:1; Rare:52 | ||||
chr4:128287701-128287837 | Rare:60 | ||||
chr4:129093458-129093747 | Common:1; Rare:85 |