Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:39635604-39635998 | Common:4; Rare:102; Clinvar:1 | ||||
chr17:39719642-39719825 | Rare:33 | ||||
chr17:39726551-39726837 | Rare:62 | ||||
chr17:39982166-39982268 | Rare:19 | ||||
chr17:39995027-39995265 | Common:1; Rare:70 | ||||
chr17:40073913-40074387 | Common:1; Rare:85 | ||||
chr17:40096083-40096220 | Rare:43 | ||||
chr17:40120680-40120905 | Rare:45 | ||||
chr17:40342954-40343015 | Rare:13 | ||||
chr17:41549794-41550098 | Common:6; Rare:59 | ||||
chr17:41579642-41579791 | Common:1; Rare:37 | ||||
chr17:41651692-41651844 | Rare:30 | ||||
chr17:41654137-41654391 | Common:2; Rare:46 | ||||
chr17:41758469-41758792 | Common:1; Rare:70; Clinvar:6; Clinvar (benign):2 | ||||
chr17:41793256-41793428 | Common:3; Rare:32 |