Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:15999605-15999831 | Common:1; Rare:120; Clinvar:4; Clinvar (benign):4 | ||||
chr17:16215532-16215677 | Common:1; Rare:62 | ||||
chr17:18039166-18039397 | Common:2; Rare:56 | ||||
chr17:18314934-18315303 | Common:1; Rare:105 | ||||
chr17:28335425-28335689 | Common:1; Rare:57 | ||||
chr17:28357474-28357646 | Common:5; Rare:79 | ||||
chr17:28662129-28662237 | Rare:41 | ||||
chr17:32350039-32350175 | Rare:67 | ||||
chr17:35242906-35243089 | Rare:61 | ||||
chr17:37406812-37406924 | Rare:42 | ||||
chr17:37489704-37489913 | Rare:83 | ||||
chr17:38296941-38297183 | Common:4; Rare:70 | ||||
chr17:39688047-39688098 | Rare:15 | ||||
chr17:42609326-42609671 | Common:8; Rare:139 | ||||
chr17:44123618-44123840 | Common:3; Rare:60 |