Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26696727-26696773 | Rare:21; Clinvar:1; Clinvar (benign):1 | ||||
chr1:26696851-26696965 | Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
chr1:26787666-26787689 | Rare:6 | ||||
chr1:26787810-26788063 | Common:3; Rare:84; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26788160-26788259 | Rare:31 | ||||
chr1:26826571-26826793 | Rare:75 | ||||
chr1:26827098-26827140 | Rare:7 | ||||
chr1:26890177-26890420 | Common:1; Rare:101 | ||||
chr1:26900023-26900250 | Rare:86 | ||||
chr1:26900374-26900620 | Rare:94 | ||||
chr1:26921525-26921921 | Common:3; Rare:123 | ||||
chr1:26921971-26922114 | Rare:33 | ||||
chr1:26922299-26922355 | Common:1; Rare:10 | ||||
chr1:26993535-26993718 | Common:5; Rare:60 | ||||
chr1:27012835-27013142 | Common:2; Rare:89 |