Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20633683-20633841 | Common:1; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
chr1:20660880-20661251 | Common:3; Rare:116; Clinvar:1; Clinvar (benign):2 | ||||
chr1:20661270-20661539 | Common:3; Rare:120; Clinvar:4; Clinvar (benign):8 | ||||
chr1:20732144-20732468 | Common:1; Rare:64 | ||||
chr1:20732995-20733365 | Common:6; Rare:77 | ||||
chr1:20775386-20775438 | Rare:12 | ||||
chr1:21174829-21174869 | Rare:10 | ||||
chr1:21345447-21345621 | Common:3; Rare:64 | ||||
chr1:21724654-21724931 | Rare:49 | ||||
chr1:21782900-21783262 | Common:2; Rare:115 | ||||
chr1:22143090-22143158 | Common:2; Rare:16 | ||||
chr1:23019364-23019569 | Rare:81 | ||||
chr1:23077121-23077355 | Common:1; Rare:50 | ||||
chr1:23344211-23344547 | Common:2; Rare:115 | ||||
chr1:23367627-23367896 | Common:1; Rare:51 |