Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:217500524-217500543 | Rare:3 | ||||
chr1:218146030-218146064 | Common:1; Rare:5 | ||||
chr1:218345228-218345415 | Common:1; Rare:32; Clinvar (benign):1 | ||||
chr1:218348154-218348299 | Common:1; Rare:41 | ||||
chr1:218680030-218680269 | Common:1; Rare:56 | ||||
chr1:219190312-219190504 | Rare:24 | ||||
chr1:220167292-220167610 | Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
chr1:220316908-220317079 | Rare:31 | ||||
chr1:220555217-220555257 | Rare:2 | ||||
chr1:220635351-220635400 | Rare:14 | ||||
chr1:221712564-221712774 | Rare:37 | ||||
chr1:221732064-221732095 | Rare:4 | ||||
chr1:221734901-221734935 | Common:1; Rare:4 | ||||
chr1:221829500-221829553 | Rare:7 | ||||
chr1:221845989-221846082 | Common:1; Rare:18 |