Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:38917272-38917385 | Common:1; Rare:14 | ||||
chr17:38921762-38922050 | Common:2; Rare:54 | ||||
chr17:40034427-40034447 | Rare:3 | ||||
chr17:40266055-40266266 | Common:1; Rare:32 | ||||
chr17:40444429-40444474 | Rare:7 | ||||
chr17:40453895-40454159 | Common:1; Rare:82 | ||||
chr17:40458884-40459159 | Common:1; Rare:52 | ||||
chr17:40463838-40464025 | Common:1; Rare:31 | ||||
chr17:40467035-40467250 | Common:4; Rare:35 | ||||
chr17:40469795-40470010 | Rare:38 | ||||
chr17:40542424-40542932 | Common:3; Rare:103 | ||||
chr17:40552121-40552348 | Common:2; Rare:58 | ||||
chr17:40552835-40553017 | Common:2; Rare:40 | ||||
chr17:40556150-40556406 | Common:1; Rare:36 | ||||
chr17:40642453-40642679 | Rare:38; Clinvar:2; Clinvar (benign):2 |