Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:179604631-179604838 | Common:1; Rare:67 | ||||
chr3:184249512-184249679 | Rare:41 | ||||
chr3:197949913-197950250 | Common:3; Rare:103; Clinvar (benign):2 | ||||
chr4:674253-674528 | Rare:125 | ||||
chr4:2468897-2469148 | Common:2; Rare:88 | ||||
chr4:4290117-4290268 | Common:3; Rare:58 | ||||
chr4:4541976-4542143 | Common:1; Rare:67 | ||||
chr4:15681458-15681863 | Common:3; Rare:141 | ||||
chr4:17810693-17811080 | Common:4; Rare:120 | ||||
chr4:38867589-38867822 | Common:2; Rare:83 | ||||
chr4:39458870-39459089 | Common:2; Rare:118; Clinvar (benign):3 | ||||
chr4:39638847-39639140 | Common:1; Rare:109 | ||||
chr4:56387450-56387531 | Rare:26 | ||||
chr4:56435560-56435742 | Common:3; Rare:62 | ||||
chr4:56435994-56436307 | Rare:111 |