Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:32350021-32350204 | Rare:99 | ||||
chr17:34961458-34961569 | Common:1; Rare:54 | ||||
chr17:35242910-35243099 | Rare:63 | ||||
chr17:35373611-35373918 | Common:4; Rare:68 | ||||
chr17:35578539-35578702 | Common:1; Rare:42; Clinvar (benign):1 | ||||
chr17:35587212-35587502 | Rare:79 | ||||
chr17:35795373-35795742 | Rare:98 | ||||
chr17:36090137-36090384 | Common:1; Rare:46 | ||||
chr17:36486476-36486716 | Common:2; Rare:85 | ||||
chr17:36534799-36535033 | Common:3; Rare:102 | ||||
chr17:36544806-36544976 | Common:2; Rare:56 | ||||
chr17:37406770-37406924 | Rare:63 | ||||
chr17:38428333-38428481 | Common:8; Rare:60 | ||||
chr17:38705035-38705334 | Common:2; Rare:71 | ||||
chr17:38706096-38706149 | Rare:27 |