Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145927364-145927657 | Common:1; Rare:76; Clinvar (pathogenic):1 | ||||
chr1:145957996-145958241 | Rare:56 | ||||
chr1:145964558-145964756 | Rare:49 | ||||
chr1:145995150-145995449 | Rare:120 | ||||
chr1:145996534-145996885 | Common:1; Rare:141 | ||||
chr1:146938247-146938480 | Common:2; Rare:76 | ||||
chr1:147172088-147172252 | Rare:42 | ||||
chr1:147172420-147172830 | Common:1; Rare:105 | ||||
chr1:147242504-147242759 | Common:4; Rare:104 | ||||
chr1:147541257-147541600 | Common:2; Rare:56 | ||||
chr1:147670228-147670269 | Rare:14 | ||||
chr1:147670462-147670695 | Common:2; Rare:56 | ||||
chr1:148152167-148152354 | Common:2; Rare:68 | ||||
chr1:148952241-148952642 | Common:5; Rare:106 | ||||
chr1:149103488-149103866 | Common:7; Rare:139 |