Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:85201693-85201790 | Common:1; Rare:38 | ||||
chr1:85582262-85582391 | Rare:33 | ||||
chr1:89910867-89911000 | Rare:23 | ||||
chr1:89953387-89953537 | Common:1; Rare:28 | ||||
chr1:90851567-90851762 | Common:2; Rare:52 | ||||
chr1:92833409-92833595 | Rare:50; Clinvar (pathogenic):1 | ||||
chr1:92835550-92835717 | Rare:24 | ||||
chr1:92840503-92840666 | Rare:44; Clinvar:1 | ||||
chr1:93160211-93160290 | Rare:21 | ||||
chr1:93576070-93576339 | Common:1; Rare:50 | ||||
chr1:93901583-93901585 | |||||
chr1:94247679-94247868 | Common:2; Rare:64 | ||||
chr1:94864105-94864257 | Rare:25 | ||||
chr1:95190475-95190690 | Common:2; Rare:46 | ||||
chr1:96796361-96796631 | Common:2; Rare:54 |