Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:38925436-38925651 | Common:4; Rare:50 | ||||
chr17:40110585-40110714 | Rare:17 | ||||
chr17:40113257-40113428 | Common:2; Rare:32 | ||||
chr17:40311091-40311251 | Rare:20 | ||||
chr17:40349712-40349822 | Rare:27 | ||||
chr17:40416391-40416817 | Rare:68; Clinvar (benign):1 | ||||
chr17:40461902-40462097 | Common:1; Rare:51 | ||||
chr17:41868711-41869046 | Common:2; Rare:61 | ||||
chr17:42275667-42275834 | Rare:35 | ||||
chr17:42299940-42300187 | Common:1; Rare:39 | ||||
chr17:42678329-42678612 | Common:1; Rare:55 | ||||
chr17:42680562-42680718 | Rare:45 | ||||
chr17:43315625-43315920 | Common:8; Rare:123 | ||||
chr17:43361334-43361361 | Common:3; Rare:18 | ||||
chr17:43368081-43368391 | Common:9; Rare:120 |