Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:204828577-204828712 | Rare:60 | ||||
chr1:205356853-205357105 | Rare:47 | ||||
chr1:205456379-205456554 | Rare:39 | ||||
chr1:205750171-205750394 | Common:2; Rare:51 | ||||
chr1:205813181-205813413 | Common:3; Rare:95 | ||||
chr1:206612443-206612631 | Common:3; Rare:51 | ||||
chr1:207052957-207053295 | Common:1; Rare:86 | ||||
chr1:207321756-207321782 | Rare:7 | ||||
chr1:207751933-207752157 | Common:1; Rare:70 | ||||
chr1:208244255-208244502 | Common:1; Rare:76 | ||||
chr1:209652421-209652625 | Common:2; Rare:44; Clinvar:1 | ||||
chr1:209675257-209675470 | Common:1; Rare:50 | ||||
chr1:209937970-209938262 | Common:3; Rare:97; Clinvar (pathogenic):1 | ||||
chr1:212035507-212035801 | Common:2; Rare:77 | ||||
chr1:212791750-212791934 | Common:4; Rare:77 |