Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:84965639-84965717 | Rare:20 | ||||
chr4:86017262-86017455 | Rare:36; Clinvar (benign):1 | ||||
chr4:88697512-88697584 | Rare:16 | ||||
chr4:90839087-90839180 | Common:1; Rare:18 | ||||
chr4:95770696-95770836 | Common:1; Rare:31 | ||||
chr4:107932115-107932177 | Common:1; Rare:17; Clinvar (benign):1 | ||||
chr4:110193743-110194046 | Rare:58 | ||||
chr4:110197463-110197693 | Rare:35 | ||||
chr4:112705783-112706127 | Common:2; Rare:77 | ||||
chr4:113214400-113214675 | Common:4; Rare:46 | ||||
chr4:113762611-113762806 | Common:3; Rare:66 | ||||
chr4:118278516-118278786 | Common:4; Rare:104 | ||||
chr4:118591661-118591818 | Rare:66 | ||||
chr4:119454556-119454939 | Common:17; Rare:129 | ||||
chr4:123649828-123649962 | Common:1; Rare:24 |