Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23825405-23825571 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23959090-23959301 | Common:3; Rare:41 | ||||
chr1:23980247-23980592 | Common:1; Rare:109 | ||||
chr1:24502266-24502344 | Rare:24 | ||||
chr1:24642882-24643335 | Common:2; Rare:149 | ||||
chr1:25232448-25232654 | Rare:82 | ||||
chr1:25819879-25820013 | Common:2; Rare:41 | ||||
chr1:26279908-26280201 | Rare:160 | ||||
chr1:26317736-26318069 | Common:3; Rare:65 | ||||
chr1:26432104-26432418 | Common:5; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472300-26472526 | Common:4; Rare:74 | ||||
chr1:26695941-26696042 | Rare:36 | ||||
chr1:26900432-26900524 | Rare:35 | ||||
chr1:27392494-27392701 | Common:1; Rare:66 | ||||
chr1:27772910-27773287 | Common:1; Rare:120 |