Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25859362-25859578 | Common:3; Rare:89 | ||||
chr1:25906397-25906593 | Rare:78 | ||||
chr1:26279948-26280158 | Rare:122 | ||||
chr1:26306590-26306834 | Common:8; Rare:63 | ||||
chr1:26432094-26432403 | Common:5; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472143-26472427 | Common:5; Rare:78 | ||||
chr1:26695726-26696047 | Common:1; Rare:105 | ||||
chr1:26862837-26863180 | Rare:71 | ||||
chr1:26900043-26900207 | Rare:62 | ||||
chr1:26900423-26900524 | Rare:41 | ||||
chr1:26921548-26921926 | Common:3; Rare:117 | ||||
chr1:26960361-26960506 | Common:1; Rare:29 | ||||
chr1:27490049-27490288 | Rare:81 | ||||
chr1:27725762-27725984 | Common:2; Rare:56 | ||||
chr1:27830505-27830838 | Common:4; Rare:94 |