Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42682429-42682529 | Rare:22 | ||||
chr17:42798637-42798767 | Rare:41 | ||||
chr17:43125370-43125694 | Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
chr17:43170965-43171259 | Common:1; Rare:98 | ||||
chr17:43211758-43211903 | Common:1; Rare:32 | ||||
chr17:44070584-44070932 | Common:3; Rare:115; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44123630-44123876 | Common:3; Rare:67 | ||||
chr17:44186701-44187037 | Rare:104 | ||||
chr17:44324780-44324980 | Common:2; Rare:71 | ||||
chr17:44899378-44899522 | Rare:58 | ||||
chr17:45051409-45051669 | Common:1; Rare:85 | ||||
chr17:45060964-45061356 | Common:2; Rare:111 | ||||
chr17:45105428-45105758 | Common:4; Rare:76 | ||||
chr17:46923049-46923187 | Common:2; Rare:54; Clinvar:1; Clinvar (benign):7 | ||||
chr17:47189250-47189577 | Rare:81 |