Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:26320590-26320827 | Common:1; Rare:88 | ||||
chr4:26320951-26321043 | Rare:39 | ||||
chr4:26860624-26860662 | Rare:13 | ||||
chr4:37826590-37826729 | Common:1; Rare:53 | ||||
chr4:38867617-38867826 | Common:2; Rare:78 | ||||
chr4:39182328-39182548 | Rare:48; Clinvar:2 | ||||
chr4:39458857-39459109 | Common:3; Rare:145; Clinvar (benign):5 | ||||
chr4:39527354-39527742 | Common:3; Rare:94 | ||||
chr4:39638838-39639140 | Common:1; Rare:112 | ||||
chr4:39697936-39698192 | Common:2; Rare:109 | ||||
chr4:41990277-41990572 | Common:2; Rare:86 | ||||
chr4:44726547-44726644 | Rare:39 | ||||
chr4:48341214-48341494 | Common:1; Rare:116 | ||||
chr4:52659268-52659439 | Common:1; Rare:55 | ||||
chr4:56387417-56387553 | Rare:44 |