Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:84730583-84730629 | Common:2; Rare:8 | ||||
chr16:85286083-85286391 | Rare:65 | ||||
chr16:85371107-85371166 | Rare:15 | ||||
chr16:85463264-85463290 | Rare:11 | ||||
chr16:85464777-85464876 | Rare:23 | ||||
chr16:85523262-85523517 | Common:3; Rare:55 | ||||
chr16:87487526-87487557 | Rare:7 | ||||
chr16:88086830-88087070 | Common:3; Rare:67 | ||||
chr16:88734479-88734699 | Common:3; Rare:106; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr17:301886-302140 | Common:3; Rare:57 | ||||
chr17:1646533-1646733 | Common:1; Rare:53 | ||||
chr17:1713910-1713995 | Rare:12 | ||||
chr17:3665045-3665181 | Common:1; Rare:17 | ||||
chr17:4074263-4074487 | Rare:56 | ||||
chr17:4586270-4586489 | Common:3; Rare:23 |