Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:3668576-3668820 | Common:1; Rare:92 | ||||
chr17:3904665-3904881 | Common:2; Rare:48 | ||||
chr17:3916455-3916587 | Rare:32 | ||||
chr17:3964426-3964586 | Common:1; Rare:60 | ||||
chr17:4142954-4143231 | Common:3; Rare:97 | ||||
chr17:4143607-4143749 | Common:4; Rare:84 | ||||
chr17:4263940-4264042 | Rare:46 | ||||
chr17:4366459-4366494 | Rare:9 | ||||
chr17:4555323-4555503 | Common:3; Rare:83 | ||||
chr17:4899353-4899659 | Common:2; Rare:158; Clinvar:9; Clinvar (benign):7; Clinvar (pathogenic):3 | ||||
chr17:4903088-4903370 | Common:2; Rare:58; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr17:4939916-4940408 | Common:2; Rare:141 | ||||
chr17:4940901-4941130 | Rare:76 | ||||
chr17:4948392-4948729 | Common:4; Rare:140 | ||||
chr17:4948943-4949181 | Common:2; Rare:82 |