Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:30893966-30894275 | Common:5; Rare:81 | ||||
chr16:46973632-46973781 | Rare:68 | ||||
chr16:47461041-47461324 | Common:2; Rare:94; Clinvar (benign):1 | ||||
chr16:53703836-53704167 | Rare:92; Clinvar:3 | ||||
chr16:56451317-56451573 | Common:1; Rare:71 | ||||
chr16:57186006-57186365 | Common:1; Rare:114 | ||||
chr16:57447360-57447493 | Common:2; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
chr16:66934365-66934494 | Rare:47 | ||||
chr16:67481136-67481281 | Common:1; Rare:50 | ||||
chr16:67528716-67528847 | Rare:36 | ||||
chr16:68310934-68311062 | Common:1; Rare:63 | ||||
chr16:69132547-69132663 | Rare:47 | ||||
chr16:69339548-69339807 | Rare:102; Clinvar (benign):1 | ||||
chr16:69726548-69726826 | Common:3; Rare:64 | ||||
chr16:70523539-70523835 | Common:3; Rare:92 |