Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:4991261-4991289 | Common:1; Rare:4 | ||||
chr17:4999752-4999966 | Rare:42; Clinvar (benign):1 | ||||
chr17:5499892-5500237 | Common:5; Rare:65 | ||||
chr17:5500239-5500623 | Common:2; Rare:75 | ||||
chr17:6649438-6649565 | Rare:15 | ||||
chr17:7176020-7176078 | Common:1; Rare:24 | ||||
chr17:7176314-7176412 | Common:2; Rare:37 | ||||
chr17:7308878-7308977 | Rare:25 | ||||
chr17:7310438-7310546 | Common:3; Rare:26 | ||||
chr17:7310780-7310985 | Rare:56 | ||||
chr17:7311023-7311189 | Rare:43 | ||||
chr17:7405885-7406015 | Common:1; Rare:26 | ||||
chr17:7414770-7415163 | Common:1; Rare:91 | ||||
chr17:7416070-7416142 | Rare:14 | ||||
chr17:7467291-7467392 | Rare:22 |