Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:236795056-236795453 | Common:6; Rare:161; Clinvar:3 | ||||
chr1:239386492-239386684 | Rare:27 | ||||
chr1:241519674-241519982 | Common:2; Rare:96; Clinvar:11; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
chr1:241639817-241639883 | Rare:21 | ||||
chr1:241848075-241848243 | Common:2; Rare:38 | ||||
chr1:243255045-243255428 | Common:1; Rare:91 | ||||
chr1:243255772-243256135 | Common:1; Rare:107; Clinvar:4; Clinvar (benign):1 | ||||
chr1:244451761-244452219 | Common:1; Rare:155 | ||||
chr1:244461256-244461385 | Common:2; Rare:37 | ||||
chr1:244835178-244835343 | Rare:65 | ||||
chr1:244835576-244835752 | Common:2; Rare:79; Clinvar (benign):5 | ||||
chr1:244856457-244856857 | Common:1; Rare:80; Clinvar (benign):2 | ||||
chr1:244863001-244863273 | Common:4; Rare:116 | ||||
chr1:244864438-244864686 | Rare:98 | ||||
chr1:244969649-244969798 | Rare:42 |