Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:9397437-9397873 | Common:1; Rare:140 | ||||
chr3:9749901-9749968 | Rare:19 | ||||
chr3:9792388-9792570 | Rare:49 | ||||
chr3:9792712-9793115 | Common:3; Rare:141 | ||||
chr3:9890503-9890685 | Common:2; Rare:69 | ||||
chr3:9933517-9933863 | Common:2; Rare:142; Clinvar:3 | ||||
chr3:10026329-10026434 | Rare:33 | ||||
chr3:11225904-11226026 | Rare:16 | ||||
chr3:12545475-12545573 | Common:1; Rare:27 | ||||
chr3:12664064-12664300 | Common:2; Rare:66; Clinvar:1; Clinvar (benign):4 | ||||
chr3:12759208-12759419 | Common:1; Rare:51 | ||||
chr3:14124703-14125160 | Common:4; Rare:135; Clinvar:4; Clinvar (benign):1 | ||||
chr3:14178517-14178870 | Common:3; Rare:180; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr3:14402284-14402722 | Common:2; Rare:107 | ||||
chr3:14651486-14651818 | Rare:98 |