Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:169583624-169583790 | Common:5; Rare:45 | ||||
chr5:172959400-172959475 | Common:1; Rare:30 | ||||
chr5:172983716-172983858 | Common:1; Rare:53 | ||||
chr5:173328394-173328602 | Rare:41 | ||||
chr5:176388563-176388806 | Common:4; Rare:92 | ||||
chr5:177022642-177022719 | Rare:24 | ||||
chr5:177497591-177497865 | Common:1; Rare:99 | ||||
chr5:179623665-179623988 | Common:4; Rare:103 | ||||
chr5:179698620-179699073 | Common:3; Rare:158 | ||||
chr6:5260734-5261010 | Common:2; Rare:88; Clinvar (benign):2 | ||||
chr6:10694604-10694984 | Common:4; Rare:101 | ||||
chr6:13615184-13615400 | Common:2; Rare:96 | ||||
chr6:24666822-24667152 | Common:2; Rare:157 | ||||
chr6:24911046-24911242 | Rare:30 | ||||
chr6:26123827-26124192 | Common:5; Rare:174 |