Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:89873523-89873654 | Rare:63 | ||||
chr16:89948661-89948803 | Common:2; Rare:37 | ||||
chr16:90022564-90022691 | Rare:49 | ||||
chr17:1516616-1516956 | Common:1; Rare:123 | ||||
chr17:1684839-1685036 | Common:2; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
chr17:2593857-2593984 | Common:1; Rare:38; Clinvar:3; Clinvar (benign):3 | ||||
chr17:3668552-3668820 | Common:2; Rare:104 | ||||
chr17:3723802-3723922 | Rare:66 | ||||
chr17:4833238-4833428 | Rare:60 | ||||
chr17:4939916-4940104 | Common:1; Rare:63 | ||||
chr17:5191838-5192096 | Common:2; Rare:84 | ||||
chr17:5419646-5419869 | Common:3; Rare:67 | ||||
chr17:5420144-5420212 | Rare:27 | ||||
chr17:5486166-5486399 | Common:4; Rare:98 | ||||
chr17:6640657-6641066 | Common:7; Rare:122 |