Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:18659755-18659875 | Rare:32 | ||||
chr10:21533964-21534365 | Common:3; Rare:166 | ||||
chr10:22316103-22316459 | Common:3; Rare:135 | ||||
chr10:23095335-23095611 | Rare:53 | ||||
chr10:24466386-24466598 | Rare:37 | ||||
chr10:25016972-25017105 | Common:4; Rare:61 | ||||
chr10:25062636-25062794 | Common:1; Rare:19 | ||||
chr10:26438060-26438416 | Common:2; Rare:82 | ||||
chr10:26438460-26438795 | Common:10; Rare:69 | ||||
chr10:27100409-27100617 | Common:3; Rare:60; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154284-27154480 | Rare:51 | ||||
chr10:27155160-27155423 | Common:7; Rare:112; Clinvar:5; Clinvar (benign):7 | ||||
chr10:27240474-27240557 | Rare:37 | ||||
chr10:27240700-27240889 | Rare:54 | ||||
chr10:27242058-27242212 | Common:1; Rare:66 |