Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42422720-42422804 | Rare:36; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr17:42422808-42422924 | Rare:43 | ||||
chr17:42574139-42574337 | Common:1; Rare:65; Clinvar:1 | ||||
chr17:42851850-42852139 | Rare:108 | ||||
chr17:43315639-43315920 | Common:7; Rare:118 | ||||
chr17:43361325-43361451 | Common:6; Rare:67 | ||||
chr17:43388308-43388676 | Common:11; Rare:65 | ||||
chr17:43860960-43861026 | Rare:11 | ||||
chr17:44088535-44088787 | Common:3; Rare:57 | ||||
chr17:44797704-44797913 | Rare:34 | ||||
chr17:45149887-45150120 | Rare:45 | ||||
chr17:45150207-45150269 | Rare:26 | ||||
chr17:47056139-47056440 | Common:4; Rare:61 | ||||
chr17:47100242-47100385 | Rare:41 | ||||
chr17:48552750-48553041 | Rare:67 |