Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:100604185-100604460 | Common:1; Rare:66 | ||||
chr7:100705952-100706133 | Common:1; Rare:69 | ||||
chr7:100852619-100852749 | Rare:35 | ||||
chr7:101217849-101218192 | Common:3; Rare:106 | ||||
chr7:102464848-102465000 | Rare:64 | ||||
chr7:103074820-103075212 | Common:7; Rare:154 | ||||
chr7:105013596-105013719 | Common:1; Rare:41 | ||||
chr7:106284936-106285256 | Common:2; Rare:115 | ||||
chr7:107563897-107564043 | Common:2; Rare:88; Clinvar (benign):5 | ||||
chr7:107744048-107744171 | Rare:40 | ||||
chr7:108569608-108570056 | Common:2; Rare:153 | ||||
chr7:112206393-112206736 | Common:1; Rare:121 | ||||
chr7:116953163-116953537 | Common:3; Rare:86 | ||||
chr7:122144237-122144437 | Common:1; Rare:39 | ||||
chr7:123748954-123749236 | Common:2; Rare:103 |