Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26279847-26280203 | Rare:191 | ||||
chr1:26432119-26432414 | Common:4; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472180-26472544 | Common:4; Rare:119 | ||||
chr1:26787865-26788201 | Common:3; Rare:94; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26900435-26900547 | Rare:37 | ||||
chr1:26921543-26921887 | Common:3; Rare:109 | ||||
chr1:27490079-27490327 | Rare:84 | ||||
chr1:27772903-27773276 | Common:1; Rare:116 | ||||
chr1:27830697-27830838 | Common:1; Rare:43 | ||||
chr1:27914528-27914812 | Common:1; Rare:110 | ||||
chr1:28088565-28088787 | Common:2; Rare:73 | ||||
chr1:28235935-28236259 | Common:3; Rare:99 | ||||
chr1:28328897-28329079 | Common:1; Rare:56 | ||||
chr1:28505801-28506056 | Common:2; Rare:96 | ||||
chr1:28552871-28553113 | Common:2; Rare:90 |