Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:17576983-17577150 | Rare:48 | ||||
chr17:17591529-17591932 | Common:2; Rare:119 | ||||
chr17:17820429-17820627 | Common:1; Rare:42 | ||||
chr17:17823581-17823834 | Common:5; Rare:116 | ||||
chr17:17972578-17972954 | Common:4; Rare:98 | ||||
chr17:18039050-18039394 | Common:3; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
chr17:18087788-18088005 | Rare:59 | ||||
chr17:18183029-18183111 | Rare:28 | ||||
chr17:18183317-18183524 | Rare:53 | ||||
chr17:18183675-18183951 | Rare:130 | ||||
chr17:18184085-18184357 | Common:1; Rare:102 | ||||
chr17:18184446-18184474 | Rare:10 | ||||
chr17:18253435-18253651 | Rare:82 | ||||
chr17:18254560-18254823 | Rare:90 | ||||
chr17:18260774-18260913 | Common:2; Rare:44 |