Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:220136702-220136912 | Rare:47; Clinvar (benign):1 | ||||
chr1:220147306-220147514 | Rare:43; Clinvar (benign):2 | ||||
chr1:220880004-220880085 | Rare:25 | ||||
chr1:222654064-222654313 | Rare:51 | ||||
chr1:222662691-222662728 | Rare:4 | ||||
chr1:222711465-222711638 | Rare:36 | ||||
chr1:222719127-222719359 | Common:1; Rare:53 | ||||
chr1:222722245-222722488 | Rare:47 | ||||
chr1:222729550-222729673 | Rare:30 | ||||
chr1:223738364-223738700 | Common:2; Rare:49 | ||||
chr1:223755263-223755638 | Rare:117 | ||||
chr1:223761892-223762246 | Common:3; Rare:82 | ||||
chr1:223766181-223766423 | Common:4; Rare:61 | ||||
chr1:223771335-223771458 | Rare:18 | ||||
chr1:223774649-223774964 | Common:2; Rare:82 |