Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:16061805-16062024 | Common:1; Rare:62 | ||||
chr17:16440191-16440251 | Rare:21 | ||||
chr17:17836186-17836418 | Common:3; Rare:63 | ||||
chr17:18184892-18185008 | Rare:23 | ||||
chr17:30238470-30238666 | Common:1; Rare:39 | ||||
chr17:31008416-31008457 | Rare:7 | ||||
chr17:31008536-31008649 | Common:2; Rare:28 | ||||
chr17:35313207-35313531 | Rare:66 | ||||
chr17:39209822-39209900 | Rare:16 | ||||
chr17:42333671-42334015 | Rare:72; Clinvar:1 | ||||
chr17:42422614-42422644 | Rare:13; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr17:42422666-42422789 | Rare:49; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr17:44797748-44797920 | Rare:28 | ||||
chr17:45149887-45150008 | Rare:25 | ||||
chr17:47100248-47100397 | Rare:39 |