Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:41611476-41611689 | Common:3; Rare:66 | ||||
chr17:41983561-41983693 | Rare:29 | ||||
chr17:42154134-42154411 | Rare:62 | ||||
chr17:42248689-42248941 | Common:4; Rare:44 | ||||
chr17:42291817-42292036 | Rare:49 | ||||
chr17:42295469-42295791 | Common:3; Rare:79 | ||||
chr17:42337516-42337794 | Common:3; Rare:69; Clinvar:1; Clinvar (benign):3 | ||||
chr17:42851695-42851907 | Common:1; Rare:92 | ||||
chr17:42851967-42852174 | Rare:77 | ||||
chr17:43010858-43011061 | Rare:33 | ||||
chr17:43315634-43315920 | Common:7; Rare:121 | ||||
chr17:43361340-43361608 | Common:6; Rare:93 | ||||
chr17:43368082-43368362 | Common:9; Rare:110 | ||||
chr17:43388301-43388443 | Rare:32 | ||||
chr17:43388554-43388676 | Common:10; Rare:19 |