Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:85799331-85799752 | Common:3; Rare:127 | ||||
chr16:87317384-87317511 | Common:3; Rare:48 | ||||
chr16:88570138-88570424 | Common:2; Rare:103 | ||||
chr16:88856932-88857153 | Common:4; Rare:97; Clinvar (benign):2 | ||||
chr16:89508321-89508420 | Rare:55; Clinvar (pathogenic):1 | ||||
chr16:89560543-89560712 | Rare:71 | ||||
chr16:89657664-89657827 | Common:1; Rare:85 | ||||
chr16:89686596-89686695 | Common:5; Rare:47 | ||||
chr16:89923130-89923352 | Rare:84 | ||||
chr16:90022578-90022703 | Rare:48 | ||||
chr17:714829-714899 | Common:1; Rare:19 | ||||
chr17:1400154-1400311 | Common:1; Rare:62 | ||||
chr17:1516610-1516954 | Common:1; Rare:122 | ||||
chr17:2303814-2303980 | Common:2; Rare:55 | ||||
chr17:2593938-2593957 | Rare:6 |