Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:1516632-1516960 | Common:1; Rare:116 | ||||
chr17:1684802-1685049 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):1 | ||||
chr17:1829805-1830071 | Common:7; Rare:112 | ||||
chr17:2071491-2071669 | Common:1; Rare:44 | ||||
chr17:2303728-2303987 | Common:2; Rare:97 | ||||
chr17:2336435-2336550 | Rare:42 | ||||
chr17:2593863-2593970 | Common:1; Rare:32; Clinvar:1; Clinvar (benign):3 | ||||
chr17:3636564-3636743 | Common:1; Rare:48; Clinvar:4; Clinvar (benign):1 | ||||
chr17:3668552-3668850 | Common:2; Rare:120 | ||||
chr17:3723764-3723926 | Common:1; Rare:90 | ||||
chr17:3892952-3893273 | Common:3; Rare:109 | ||||
chr17:4143042-4143218 | Rare:56 | ||||
chr17:4263943-4264065 | Rare:49 | ||||
chr17:4555331-4555537 | Common:3; Rare:93 | ||||
chr17:4704107-4704211 | Rare:60 |