Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145927364-145927587 | Common:1; Rare:55; Clinvar (pathogenic):1 | ||||
chr1:145957969-145958223 | Rare:64 | ||||
chr1:145964567-145964767 | Rare:48 | ||||
chr1:145994915-145995485 | Rare:238 | ||||
chr1:145995998-145996631 | Common:1; Rare:252 | ||||
chr1:145996651-145996852 | Common:1; Rare:70 | ||||
chr1:146228968-146229182 | Common:2; Rare:46 | ||||
chr1:147172393-147172815 | Common:1; Rare:113 | ||||
chr1:147242528-147242742 | Common:3; Rare:93 | ||||
chr1:149886628-149887189 | Common:3; Rare:218 | ||||
chr1:149887947-149888215 | Rare:62 | ||||
chr1:149927760-149927940 | Common:1; Rare:71; Clinvar (benign):4 | ||||
chr1:150010510-150010676 | Common:2; Rare:34 | ||||
chr1:150067207-150067373 | Common:3; Rare:34 | ||||
chr1:150067559-150067860 | Common:1; Rare:85 |