Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42833302-42833497 | Rare:73 | ||||
chr17:42964428-42964515 | Rare:42 | ||||
chr17:43125474-43125647 | Rare:42; Clinvar (benign):1 | ||||
chr17:43170284-43170712 | Common:3; Rare:83 | ||||
chr17:43171002-43171255 | Rare:84 | ||||
chr17:43778894-43779062 | Rare:40 | ||||
chr17:44070612-44070947 | Common:3; Rare:116; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44111135-44111446 | Rare:95 | ||||
chr17:44123579-44123840 | Common:3; Rare:75 | ||||
chr17:44170547-44170747 | Rare:37 | ||||
chr17:44186662-44187002 | Common:1; Rare:123 | ||||
chr17:44324771-44324989 | Common:2; Rare:79 | ||||
chr17:44345075-44345321 | Rare:51; Clinvar:5; Clinvar (benign):3 | ||||
chr17:44436512-44436649 | Rare:29 | ||||
chr17:44503365-44503665 | Rare:123 |