Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:119648138-119648350 | Common:3; Rare:77 | ||||
chr1:145823922-145824268 | Rare:123 | ||||
chr1:145858994-145859173 | Rare:51 | ||||
chr1:145918658-145919043 | Common:2; Rare:94; Clinvar:1 | ||||
chr1:145927413-145927612 | Common:1; Rare:55; Clinvar (pathogenic):1 | ||||
chr1:145964573-145964749 | Rare:44 | ||||
chr1:147172419-147172785 | Common:1; Rare:94 | ||||
chr1:148952027-148952146 | Common:3; Rare:33 | ||||
chr1:148952271-148952402 | Common:1; Rare:43 | ||||
chr1:148952566-148952664 | Common:1; Rare:12 | ||||
chr1:149886677-149886996 | Common:1; Rare:111 | ||||
chr1:149887952-149888214 | Rare:57 | ||||
chr1:149927756-149927869 | Rare:49; Clinvar (benign):4 | ||||
chr1:150067559-150067844 | Common:1; Rare:76 | ||||
chr1:150236083-150236366 | Rare:61 |