Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145918680-145919043 | Common:2; Rare:82 | ||||
chr1:145927364-145927634 | Common:1; Rare:68; Clinvar (pathogenic):1 | ||||
chr1:145957996-145958191 | Rare:43 | ||||
chr1:145964587-145964742 | Rare:37 | ||||
chr1:145995142-145995479 | Rare:131 | ||||
chr1:145996015-145996310 | Rare:134 | ||||
chr1:145996412-145996885 | Common:2; Rare:175 | ||||
chr1:146228922-146229233 | Common:3; Rare:72 | ||||
chr1:146938308-146938343 | Rare:17 | ||||
chr1:147172420-147172779 | Common:1; Rare:92 | ||||
chr1:148458624-148459001 | Common:2; Rare:93 | ||||
chr1:148679713-148679924 | Rare:20 | ||||
chr1:148951772-148952146 | Common:5; Rare:78 | ||||
chr1:148952222-148952488 | Common:4; Rare:85 | ||||
chr1:149390419-149390625 | Rare:26 |