Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:185045250-185045632 | Common:2; Rare:132 | ||||
chr1:185156600-185157303 | Common:3; Rare:230 | ||||
chr1:185157409-185157544 | Common:1; Rare:40 | ||||
chr1:185317186-185317649 | Common:2; Rare:126 | ||||
chr1:186375099-186375928 | Common:1; Rare:232 | ||||
chr1:186680405-186680688 | Common:3; Rare:61 | ||||
chr1:190474805-190474977 | Common:1; Rare:36 | ||||
chr1:192158285-192158517 | Common:1; Rare:42 | ||||
chr1:192808794-192809138 | Common:4; Rare:151 | ||||
chr1:193059298-193059770 | Common:1; Rare:222 | ||||
chr1:193105373-193105491 | Common:2; Rare:45 | ||||
chr1:193121780-193122210 | Common:2; Rare:151; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:193186560-193186657 | Rare:16 | ||||
chr1:196651923-196652172 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):3 | ||||
chr1:197902545-197902652 | Common:1; Rare:35 |