Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154607991-154608022 | Rare:9 | ||||
chr1:154608052-154608456 | Common:3; Rare:96; Clinvar (benign):1 | ||||
chr1:154608637-154608963 | Common:9; Rare:69 | ||||
chr1:154627319-154627461 | Common:1; Rare:32 | ||||
chr1:154627844-154628074 | Common:5; Rare:104 | ||||
chr1:154936401-154937069 | Common:3; Rare:156 | ||||
chr1:154937215-154937467 | Common:1; Rare:64 | ||||
chr1:154955657-154955892 | Common:1; Rare:35 | ||||
chr1:154956032-154956284 | Common:1; Rare:74 | ||||
chr1:154961483-154961605 | Rare:37 | ||||
chr1:154961684-154961874 | Common:1; Rare:78 | ||||
chr1:154961908-154962104 | Rare:54 | ||||
chr1:154970695-154970852 | Rare:31 | ||||
chr1:154973618-154974246 | Common:3; Rare:156 | ||||
chr1:154974280-154974710 | Rare:98 |