Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:192808794-192809060 | Common:4; Rare:104 | ||||
chr1:193059330-193059689 | Rare:169 | ||||
chr1:193121771-193122239 | Common:2; Rare:169; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr1:197902574-197902644 | Rare:21 | ||||
chr1:200042453-200042704 | Common:2; Rare:55 | ||||
chr1:200669842-200670131 | Common:12; Rare:94 | ||||
chr1:201154457-201154627 | Common:2; Rare:44 | ||||
chr1:201399282-201399659 | Common:1; Rare:139 | ||||
chr1:201739724-201739900 | Rare:33 | ||||
chr1:201946453-201946793 | Common:2; Rare:55 | ||||
chr1:201982482-201982663 | Common:1; Rare:63 | ||||
chr1:202010348-202010629 | Common:2; Rare:65 | ||||
chr1:203305265-203305538 | Common:3; Rare:70 | ||||
chr1:203306014-203306310 | Common:2; Rare:68 | ||||
chr1:203626674-203626841 | Common:1; Rare:44 |