Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:156674377-156674635 | Common:3; Rare:73 | ||||
chr3:179604632-179604836 | Common:1; Rare:65 | ||||
chr3:184135353-184135393 | Rare:12 | ||||
chr3:193593119-193593247 | Rare:40 | ||||
chr3:197949887-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
chr4:674253-674574 | Common:2; Rare:149 | ||||
chr4:4541978-4542143 | Common:1; Rare:65 | ||||
chr4:15681521-15681856 | Common:3; Rare:117 | ||||
chr4:26320896-26321028 | Rare:46; Clinvar (benign):1 | ||||
chr4:39458853-39459075 | Common:3; Rare:123; Clinvar (benign):1 | ||||
chr4:39638847-39639140 | Common:1; Rare:109 | ||||
chr4:56467519-56467632 | Rare:45 | ||||
chr4:67701121-67701284 | Common:2; Rare:80 | ||||
chr4:75514268-75514483 | Common:1; Rare:72 | ||||
chr4:75724436-75724687 | Common:1; Rare:73 |