Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:184386886-184387193 | Common:1; Rare:78 | ||||
chr1:185156710-185156748 | Rare:20 | ||||
chr1:185156934-185157303 | Common:1; Rare:100 | ||||
chr1:185317196-185317468 | Common:1; Rare:81 | ||||
chr1:186375112-186375491 | Rare:106 | ||||
chr1:186375656-186375892 | Common:1; Rare:63 | ||||
chr1:186680286-186680670 | Common:3; Rare:90 | ||||
chr1:192808905-192809064 | Common:3; Rare:64 | ||||
chr1:193059280-193059476 | Rare:86 | ||||
chr1:193059481-193059690 | Rare:106 | ||||
chr1:193186568-193186645 | Rare:12 | ||||
chr1:200669976-200670273 | Common:1; Rare:65 | ||||
chr1:200894807-200894926 | Rare:23 | ||||
chr1:201154457-201154627 | Common:2; Rare:44 | ||||
chr1:201283210-201283616 | Common:3; Rare:88; Clinvar:2; Clinvar (benign):1 |