Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:30600332-30600422 | Common:4; Rare:20 | ||||
chr17:31008494-31008634 | Common:2; Rare:32 | ||||
chr17:35567938-35568153 | Common:1; Rare:59 | ||||
chr17:40120813-40120948 | Rare:30 | ||||
chr17:42050593-42050834 | Common:1; Rare:64 | ||||
chr17:42333734-42334015 | Rare:59; Clinvar:1 | ||||
chr17:43315645-43315920 | Common:7; Rare:118 | ||||
chr17:45247815-45247963 | Common:1; Rare:29 | ||||
chr17:45895575-45895791 | Common:2; Rare:55 | ||||
chr17:47100267-47100399 | Rare:32 | ||||
chr17:47492444-47492753 | Common:3; Rare:105 | ||||
chr17:49192873-49193128 | Common:3; Rare:66 | ||||
chr17:50189430-50189683 | Rare:59; Clinvar:3; Clinvar (benign):2 | ||||
chr17:50565883-50565983 | Rare:25 | ||||
chr17:57486938-57487078 | Rare:22 |