Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:186375664-186375942 | Common:1; Rare:75 | ||||
chr1:186680294-186680763 | Common:3; Rare:108 | ||||
chr1:186828708-186829024 | Common:1; Rare:82 | ||||
chr1:192808784-192809190 | Common:4; Rare:163; Clinvar:1 | ||||
chr1:193059185-193059770 | Common:1; Rare:252 | ||||
chr1:193121916-193122326 | Common:1; Rare:125; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr1:197902551-197902619 | Rare:24 | ||||
chr1:200409977-200410237 | Rare:82 | ||||
chr1:200654834-200654974 | Rare:20 | ||||
chr1:200669776-200670177 | Common:12; Rare:126 | ||||
chr1:200738716-200739104 | Common:6; Rare:114 | ||||
chr1:200739208-200739611 | Common:1; Rare:92 | ||||
chr1:200739710-200739870 | Rare:45 | ||||
chr1:201283243-201283918 | Common:4; Rare:187; Clinvar:5; Clinvar (benign):2 | ||||
chr1:201399264-201399763 | Common:1; Rare:177 |