Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161098238-161098511 | Common:2; Rare:60 | ||||
chr1:161117502-161117668 | Rare:36 | ||||
chr1:161117946-161118206 | Rare:128 | ||||
chr1:161132507-161133296 | Common:3; Rare:190 | ||||
chr1:161153686-161154310 | Common:2; Rare:178; Clinvar (pathogenic):1 | ||||
chr1:161159362-161159601 | Common:2; Rare:79 | ||||
chr1:161166205-161166606 | Common:4; Rare:100; Clinvar:5; Clinvar (benign):2 | ||||
chr1:161177169-161177275 | Rare:33 | ||||
chr1:161177412-161177782 | Common:1; Rare:99 | ||||
chr1:161177796-161177838 | Rare:4 | ||||
chr1:161195239-161195472 | Rare:44 | ||||
chr1:161202106-161202512 | Common:3; Rare:126; Clinvar:5; Clinvar (benign):10 | ||||
chr1:161225678-161226131 | Common:10; Rare:80 | ||||
chr1:161226580-161226746 | Rare:37 | ||||
chr1:161227453-161227650 | Rare:37 |