Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25859351-25859549 | Common:3; Rare:84 | ||||
chr1:25906392-25906593 | Rare:79 | ||||
chr1:26306620-26306861 | Common:13; Rare:74 | ||||
chr1:26432119-26432385 | Common:4; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472293-26472528 | Common:4; Rare:76 | ||||
chr1:26787663-26787994 | Common:3; Rare:109; Clinvar:1; Clinvar (benign):2 | ||||
chr1:26900438-26900513 | Rare:29 | ||||
chr1:26921529-26921815 | Common:3; Rare:88 | ||||
chr1:27725669-27725984 | Common:3; Rare:88 | ||||
chr1:27830662-27830831 | Common:3; Rare:56 | ||||
chr1:28328897-28329073 | Common:1; Rare:54 | ||||
chr1:28505815-28506064 | Common:2; Rare:100 | ||||
chr1:28552871-28553113 | Common:2; Rare:90 | ||||
chr1:28642997-28643164 | Rare:68 | ||||
chr1:28736653-28737010 | Common:3; Rare:121 |