Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:52921513-52921669 | Common:1; Rare:62 | ||||
chr1:52921723-52921875 | Rare:33 | ||||
chr1:52927160-52927327 | Common:3; Rare:48 | ||||
chr1:53014866-53015008 | Rare:41 | ||||
chr1:53196624-53196861 | Common:1; Rare:79; Clinvar:6; Clinvar (benign):1 | ||||
chr1:53220189-53220395 | Rare:107 | ||||
chr1:53220584-53220780 | Common:2; Rare:78 | ||||
chr1:53238457-53238752 | Common:2; Rare:101 | ||||
chr1:53328063-53328278 | Rare:51 | ||||
chr1:53838052-53838152 | Common:1; Rare:23 | ||||
chr1:53838161-53838347 | Rare:77 | ||||
chr1:53838393-53838756 | Rare:86 | ||||
chr1:53889747-53890005 | Common:2; Rare:81 | ||||
chr1:53945551-53945654 | Rare:23 | ||||
chr1:53945809-53946109 | Common:4; Rare:81 |