Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25819875-25820013 | Common:2; Rare:42 | ||||
chr1:25859370-25859580 | Common:2; Rare:85 | ||||
chr1:26279953-26280162 | Rare:121 | ||||
chr1:26432112-26432422 | Common:4; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26787865-26787994 | Common:3; Rare:42; Clinvar:1; Clinvar (benign):2 | ||||
chr1:26862872-26863208 | Rare:76 | ||||
chr1:26900435-26900527 | Rare:34 | ||||
chr1:26921554-26921832 | Common:3; Rare:89 | ||||
chr1:26960366-26960504 | Common:1; Rare:27 | ||||
chr1:27725760-27725998 | Common:2; Rare:63 | ||||
chr1:27830629-27830841 | Common:3; Rare:70 | ||||
chr1:28088551-28088818 | Common:3; Rare:94 | ||||
chr1:28328914-28329063 | Common:1; Rare:45 | ||||
chr1:28505815-28506050 | Common:2; Rare:91 | ||||
chr1:28552780-28553113 | Common:2; Rare:107 |