Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:52921522-52921571 | Common:1; Rare:17 | ||||
chr1:52927170-52927465 | Common:4; Rare:99; Clinvar:2 | ||||
chr1:53196668-53197081 | Rare:158; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
chr1:53220586-53220760 | Common:2; Rare:71 | ||||
chr1:53238460-53238695 | Common:2; Rare:88 | ||||
chr1:53889732-53889986 | Common:2; Rare:81 | ||||
chr1:53946260-53946455 | Rare:72 | ||||
chr1:54053000-54053646 | Common:7; Rare:220 | ||||
chr1:54199977-54200361 | Rare:125 | ||||
chr1:54200515-54200588 | Rare:21 | ||||
chr1:54801295-54801381 | Rare:13 | ||||
chr1:54886702-54886862 | Rare:55 | ||||
chr1:54886887-54887057 | Common:1; Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
chr1:54887069-54887237 | Common:1; Rare:73; Clinvar:4; Clinvar (benign):1 | ||||
chr1:56579040-56579141 | Rare:31 |