Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:84965637-84965717 | Rare:20 | ||||
chr4:86844875-86845159 | Common:1; Rare:46 | ||||
chr4:86847733-86847842 | Rare:16 | ||||
chr4:87490759-87491057 | Rare:67 | ||||
chr4:99316048-99316292 | Rare:81 | ||||
chr4:99436623-99436768 | Rare:21 | ||||
chr4:110195503-110195799 | Common:2; Rare:50 | ||||
chr4:118279109-118279190 | Common:3; Rare:20 | ||||
chr4:119454554-119454911 | Common:17; Rare:121 | ||||
chr4:139177903-139178148 | Rare:77 | ||||
chr4:147733582-147733918 | Common:1; Rare:60 | ||||
chr4:153684067-153684348 | Common:2; Rare:83 | ||||
chr4:168890712-168891057 | Common:1; Rare:82; Clinvar:4; Clinvar (benign):2 | ||||
chr4:168924032-168924418 | Rare:94; Clinvar:4; Clinvar (benign):1 | ||||
chr4:183798086-183798315 | Common:5; Rare:52 |