Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:89972485-89972635 | Common:1; Rare:58 | ||||
chr17:714780-714941 | Common:2; Rare:55 | ||||
chr17:752222-752314 | Common:2; Rare:37 | ||||
chr17:979714-979987 | Common:3; Rare:132 | ||||
chr17:1491608-1491816 | Common:1; Rare:63 | ||||
chr17:1516588-1516968 | Common:2; Rare:133 | ||||
chr17:1684780-1685057 | Common:2; Rare:91; Clinvar:7; Clinvar (benign):1 | ||||
chr17:1829822-1830039 | Common:6; Rare:91 | ||||
chr17:2303503-2303643 | Rare:50 | ||||
chr17:2303764-2303980 | Common:2; Rare:79 | ||||
chr17:2336423-2336552 | Rare:50 | ||||
chr17:2392607-2392913 | Common:7; Rare:144 | ||||
chr17:2511806-2511979 | Common:2; Rare:50 | ||||
chr17:2593507-2593658 | Common:2; Rare:48 | ||||
chr17:3636218-3636459 | Common:4; Rare:74; Clinvar (benign):1 |