Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:43211676-43211911 | Common:2; Rare:55 | ||||
chr17:44070523-44070965 | Common:3; Rare:138; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44123594-44123834 | Common:3; Rare:71 | ||||
chr17:44186687-44187029 | Common:1; Rare:114 | ||||
chr17:44187153-44187297 | Rare:36 | ||||
chr17:44198401-44198545 | Common:2; Rare:33 | ||||
chr17:44209370-44209686 | Rare:80 | ||||
chr17:44210182-44210436 | Common:2; Rare:87 | ||||
chr17:44211115-44211304 | Common:1; Rare:60 | ||||
chr17:44324774-44325039 | Common:2; Rare:92 | ||||
chr17:44557052-44557457 | Common:2; Rare:76 | ||||
chr17:44557474-44557769 | Common:1; Rare:99 | ||||
chr17:44899371-44899764 | Common:3; Rare:124; Clinvar:3; Clinvar (benign):1 | ||||
chr17:45060933-45061457 | Common:3; Rare:151 | ||||
chr17:45132493-45132631 | Common:1; Rare:45 |