Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:50314489-50314643 | Common:1; Rare:70 | ||||
chr22:50538330-50538531 | Common:1; Rare:44 | ||||
chr22:50539657-50539916 | Common:3; Rare:44 | ||||
chr22:50541806-50541942 | Rare:30 | ||||
chr22:50542605-50542718 | Common:2; Rare:25 | ||||
chr22:50548654-50548813 | Common:1; Rare:59 | ||||
chr3:4977107-4977450 | Rare:63 | ||||
chr3:4986833-4987080 | Common:1; Rare:55 | ||||
chr3:5122855-5123156 | Common:1; Rare:90 | ||||
chr3:9684950-9685247 | Rare:79; Clinvar (benign):1 | ||||
chr3:10193066-10193283 | Common:1; Rare:45 | ||||
chr3:11289207-11289353 | Common:1; Rare:31 | ||||
chr3:12188002-12188184 | Common:1; Rare:26 | ||||
chr3:12193541-12193841 | Common:1; Rare:46 | ||||
chr3:12647728-12647891 | Common:1; Rare:31 |