Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154567644-154568018 | Common:4; Rare:90; Clinvar (benign):2 | ||||
chr1:154627862-154628018 | Common:3; Rare:80 | ||||
chr1:154870235-154870489 | Rare:56 | ||||
chr1:154936631-154936670 | Rare:13 | ||||
chr1:154956085-154956235 | Common:1; Rare:42 | ||||
chr1:154961482-154961817 | Rare:112 | ||||
chr1:154970731-154970869 | Rare:24 | ||||
chr1:154974374-154974744 | Rare:100 | ||||
chr1:154983097-154983393 | Common:2; Rare:57; Clinvar (benign):1 | ||||
chr1:155127604-155127890 | Common:1; Rare:53 | ||||
chr1:155135734-155135886 | Common:1; Rare:63 | ||||
chr1:155140507-155140610 | Common:3; Rare:32; Clinvar:1 | ||||
chr1:155173130-155173364 | Common:3; Rare:105 | ||||
chr1:155173600-155173934 | Rare:62 | ||||
chr1:155174359-155174611 | Rare:60 |