Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:10729980-10730099 | Common:3; Rare:28 | ||||
chr17:13017969-13018284 | Common:6; Rare:95; Clinvar (benign):1 | ||||
chr17:14069395-14069577 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):3 | ||||
chr17:15699547-15699768 | Common:3; Rare:60 | ||||
chr17:15999610-15999980 | Common:3; Rare:169; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
chr17:16215532-16215639 | Common:1; Rare:47 | ||||
chr17:16217139-16217240 | Rare:31; Clinvar:1 | ||||
chr17:16415414-16415585 | Rare:27 | ||||
chr17:17281194-17281422 | Rare:89 | ||||
chr17:17496388-17496553 | Rare:41 | ||||
chr17:17591604-17591650 | Rare:13 | ||||
chr17:17591652-17591922 | Common:1; Rare:75 | ||||
chr17:18039155-18039387 | Common:3; Rare:57; Clinvar (benign):1 | ||||
chr17:18087807-18087999 | Rare:54 | ||||
chr17:18183803-18183931 | Rare:53 |