Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:99655710-99655882 | Rare:31 | ||||
chr4:110621491-110621761 | Common:2; Rare:61 | ||||
chr4:118279109-118279190 | Common:3; Rare:20 | ||||
chr4:118976067-118976244 | Common:2; Rare:45 | ||||
chr4:118976461-118976709 | Common:1; Rare:81 | ||||
chr4:118989527-118989738 | Rare:47 | ||||
chr4:118997703-118997813 | Common:1; Rare:18 | ||||
chr4:119010959-119011247 | Common:1; Rare:43 | ||||
chr4:119027883-119028050 | Common:1; Rare:30 | ||||
chr4:119145623-119145860 | Common:1; Rare:37 | ||||
chr4:119150757-119151041 | Common:2; Rare:65; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr4:119454583-119454861 | Common:13; Rare:96 | ||||
chr4:121071330-121071349 | Rare:6 | ||||
chr4:124020161-124020385 | Common:1; Rare:40 | ||||
chr4:143186228-143186290 | Rare:10 |