Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20661340-20661663 | Common:3; Rare:118; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786564-20786870 | Rare:111 | ||||
chr1:20787206-20787465 | Rare:121 | ||||
chr1:21176848-21177047 | Rare:57 | ||||
chr1:21345439-21345663 | Common:3; Rare:82 | ||||
chr1:21833610-21833842 | Common:4; Rare:47; Clinvar:1; Clinvar (benign):2 | ||||
chr1:21854609-21854872 | Common:2; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
chr1:21874503-21874733 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
chr1:22451644-22451868 | Common:1; Rare:72 | ||||
chr1:23344233-23344458 | Common:2; Rare:80 | ||||
chr1:23558933-23559671 | Common:7; Rare:336 | ||||
chr1:23800730-23800959 | Common:1; Rare:80 | ||||
chr1:23959035-23959304 | Common:3; Rare:50 | ||||
chr1:23959641-23959868 | Common:2; Rare:63 | ||||
chr1:23980189-23980473 | Rare:75 |