Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20650301-20650523 | Common:3; Rare:62; Clinvar (benign):1 | ||||
chr1:22025185-22025518 | Common:7; Rare:82 | ||||
chr1:31373704-31373889 | Common:1; Rare:35 | ||||
chr1:32612195-32612275 | Rare:13 | ||||
chr1:36179731-36179927 | Rare:45 | ||||
chr1:39632947-39633288 | Common:1; Rare:81 | ||||
chr1:51794823-51794885 | Common:1; Rare:13 | ||||
chr1:56577828-56577981 | Common:2; Rare:31 | ||||
chr1:58782265-58782538 | Common:1; Rare:89; Clinvar:1 | ||||
chr1:67831950-67832224 | Common:1; Rare:60 | ||||
chr1:90851562-90851782 | Common:2; Rare:56 | ||||
chr1:100158212-100158537 | Common:1; Rare:94 | ||||
chr1:116418566-116418670 | Common:1; Rare:35 | ||||
chr1:149196554-149196743 | Rare:14 | ||||
chr1:149198000-149198132 | Rare:8 |