Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43119963-43120180 | Common:7; Rare:73 | ||||
chr1:44336735-44336897 | Rare:28 | ||||
chr1:44649502-44649722 | Rare:58 | ||||
chr1:46279009-46279256 | Rare:59 | ||||
chr1:46332176-46332345 | Common:2; Rare:42 | ||||
chr1:46717933-46718098 | Rare:49 | ||||
chr1:51787162-51787485 | Rare:69 | ||||
chr1:53524995-53525035 | Rare:9 | ||||
chr1:54564357-54564584 | Common:1; Rare:54 | ||||
chr1:58576122-58576442 | Common:3; Rare:114; Clinvar:3; Clinvar (benign):3 | ||||
chr1:58782226-58782316 | Rare:12 | ||||
chr1:58783096-58783130 | Common:1; Rare:9 | ||||
chr1:65067713-65067871 | Rare:43 | ||||
chr1:67831950-67832224 | Common:1; Rare:60 | ||||
chr1:71078506-71078614 | Rare:22 |