Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:28842770-28842864 | Rare:31 | ||||
chr17:29568514-29568740 | Common:2; Rare:72 | ||||
chr17:30477250-30477427 | Common:1; Rare:46 | ||||
chr17:32350026-32350204 | Rare:98 | ||||
chr17:34961423-34961561 | Rare:67 | ||||
chr17:35242910-35243081 | Rare:57 | ||||
chr17:35578550-35578715 | Common:1; Rare:44; Clinvar (benign):1 | ||||
chr17:35587231-35587478 | Rare:68 | ||||
chr17:36534803-36535033 | Common:3; Rare:102 | ||||
chr17:37406823-37406924 | Rare:36 | ||||
chr17:37489709-37489912 | Rare:79 | ||||
chr17:38752487-38752826 | Common:4; Rare:89 | ||||
chr17:38825292-38825408 | Common:1; Rare:33 | ||||
chr17:38853683-38853875 | Common:2; Rare:78 | ||||
chr17:39200007-39200349 | Common:2; Rare:106 |