Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:14300765-14301167 | Common:3; Rare:105 | ||||
chr17:15563422-15563793 | Common:1; Rare:130 | ||||
chr17:15651846-15651892 | Rare:8 | ||||
chr17:15684220-15684469 | Common:3; Rare:70 | ||||
chr17:15699442-15699826 | Common:5; Rare:109 | ||||
chr17:15999436-15999529 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):2 | ||||
chr17:15999544-15999885 | Common:3; Rare:172; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
chr17:16000282-16000320 | Common:1; Rare:11 | ||||
chr17:16215023-16215152 | Rare:35 | ||||
chr17:16215424-16215789 | Common:3; Rare:150 | ||||
chr17:16215878-16216117 | Common:5; Rare:73 | ||||
chr17:16217010-16217276 | Rare:76; Clinvar:2 | ||||
chr17:16352760-16352966 | Common:1; Rare:48 | ||||
chr17:16353407-16353650 | Rare:74 | ||||
chr17:16380687-16380802 | Common:2; Rare:24 |