Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:183635660-183636100 | Common:4; Rare:125 | ||||
chr1:184051601-184051768 | Common:3; Rare:63 | ||||
chr1:184386740-184387123 | Common:3; Rare:119 | ||||
chr1:184754779-184755161 | Common:1; Rare:94 | ||||
chr1:185156923-185157303 | Common:1; Rare:105 | ||||
chr1:186375123-186375430 | Rare:84 | ||||
chr1:186375656-186375920 | Common:1; Rare:69 | ||||
chr1:192808809-192809045 | Common:4; Rare:91 | ||||
chr1:193059321-193059697 | Rare:176 | ||||
chr1:193105373-193105491 | Common:2; Rare:45 | ||||
chr1:193121771-193122210 | Common:2; Rare:157; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:197146593-197146794 | Rare:49; Clinvar:3 | ||||
chr1:197902614-197902647 | Rare:9 | ||||
chr1:201946501-201946664 | Common:2; Rare:25 | ||||
chr1:201955389-201955529 | Rare:42 |