Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42323585-42323738 | Common:2; Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
chr17:42329459-42329702 | Common:2; Rare:71; Clinvar (benign):2 | ||||
chr17:42387307-42387475 | Rare:31 | ||||
chr17:42422821-42422914 | Rare:39 | ||||
chr17:42575734-42575823 | Rare:19 | ||||
chr17:42666109-42666354 | Common:2; Rare:62 | ||||
chr17:43160010-43160134 | Rare:15 | ||||
chr17:43193245-43193363 | Rare:26 | ||||
chr17:43315650-43315944 | Common:8; Rare:142 | ||||
chr17:43368075-43368391 | Common:10; Rare:128 | ||||
chr17:43523579-43523680 | Rare:34 | ||||
chr17:44215703-44215960 | Common:1; Rare:59 | ||||
chr17:44454053-44454161 | Rare:17 | ||||
chr17:44463283-44463338 | Rare:5 | ||||
chr17:44559349-44559440 | Rare:27 |