Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26472266-26472539 | Common:4; Rare:93 | ||||
chr1:26787865-26787974 | Common:1; Rare:36; Clinvar (benign):1 | ||||
chr1:26890229-26890373 | Common:1; Rare:57 | ||||
chr1:26900435-26900526 | Rare:34 | ||||
chr1:26921529-26921837 | Common:3; Rare:98 | ||||
chr1:27321983-27322327 | Common:1; Rare:124 | ||||
chr1:27725657-27725988 | Common:3; Rare:90 | ||||
chr1:27772920-27773351 | Common:1; Rare:141 | ||||
chr1:27830709-27830878 | Common:1; Rare:70 | ||||
chr1:27872401-27872565 | Rare:47 | ||||
chr1:27914528-27914908 | Common:1; Rare:140 | ||||
chr1:28088565-28088801 | Common:3; Rare:80 | ||||
chr1:28235946-28236220 | Common:3; Rare:87 | ||||
chr1:28328892-28329109 | Common:1; Rare:69 | ||||
chr1:28369580-28369786 | Common:2; Rare:84 |