Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42456244-42456578 | Common:1; Rare:98 | ||||
chr1:42658295-42658480 | Common:2; Rare:56 | ||||
chr1:42682125-42682465 | Common:2; Rare:94 | ||||
chr1:42682606-42682731 | Common:1; Rare:52 | ||||
chr1:42766996-42767312 | Common:4; Rare:107; Clinvar (benign):1 | ||||
chr1:42816985-42817112 | Common:1; Rare:34 | ||||
chr1:42846381-42846655 | Common:1; Rare:80 | ||||
chr1:42958834-42959042 | Common:3; Rare:58; Clinvar:5; Clinvar (benign):4 | ||||
chr1:43358662-43359014 | Common:7; Rare:113 | ||||
chr1:43367986-43368212 | Rare:60 | ||||
chr1:43389765-43389946 | Common:3; Rare:77 | ||||
chr1:43649879-43650173 | Rare:71 | ||||
chr1:43707332-43707593 | Common:2; Rare:80 | ||||
chr1:43974781-43975026 | Common:3; Rare:65 | ||||
chr1:44213303-44213548 | Common:2; Rare:54 |