Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:197850988-197851013 | Rare:3 | ||||
chr4:781795-782140 | Common:2; Rare:119 | ||||
chr4:1167586-1167795 | Common:2; Rare:89 | ||||
chr4:6673837-6673936 | Common:5; Rare:52 | ||||
chr4:7103380-7103555 | Common:3; Rare:39 | ||||
chr4:15005031-15005086 | Rare:27 | ||||
chr4:15599375-15599592 | Rare:51; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr4:20251750-20251909 | Common:1; Rare:63 | ||||
chr4:30719348-30719721 | Common:1; Rare:85 | ||||
chr4:48342088-48342120 | Rare:7 | ||||
chr4:55438469-55438663 | Rare:56 | ||||
chr4:57033281-57033552 | Common:1; Rare:56 | ||||
chr4:71186558-71186767 | Common:1; Rare:56 | ||||
chr4:75725191-75725249 | Rare:18 | ||||
chr4:76306552-76306800 | Rare:79 |