Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:9792789-9793123 | Common:3; Rare:117 | ||||
chr3:9843968-9844135 | Common:2; Rare:66 | ||||
chr3:9986777-9987163 | Common:3; Rare:108 | ||||
chr3:10026329-10026455 | Rare:38 | ||||
chr3:11154296-11154528 | Common:4; Rare:62 | ||||
chr3:12288955-12289075 | Rare:22 | ||||
chr3:12484334-12484511 | Common:4; Rare:55; Clinvar (benign):1 | ||||
chr3:12664068-12664330 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):3 | ||||
chr3:13549009-13549199 | Rare:66 | ||||
chr3:14124714-14125173 | Common:4; Rare:134; Clinvar:4; Clinvar (benign):1 | ||||
chr3:14178565-14178879 | Common:2; Rare:163; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr3:14651486-14651801 | Rare:90 | ||||
chr3:14947244-14947554 | Common:3; Rare:143 | ||||
chr3:15205988-15206279 | Rare:106 | ||||
chr3:15427478-15427629 | Common:1; Rare:51 |