Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:18254577-18254824 | Rare:86 | ||||
chr17:18314928-18315332 | Common:1; Rare:117 | ||||
chr17:18781075-18781310 | Common:5; Rare:64 | ||||
chr17:19004733-19004878 | Common:1; Rare:49 | ||||
chr17:19377899-19378035 | Common:1; Rare:32 | ||||
chr17:19378170-19378545 | Common:2; Rare:92 | ||||
chr17:19648648-19649007 | Common:3; Rare:126; Clinvar (benign):1 | ||||
chr17:19977804-19977974 | Common:1; Rare:58 | ||||
chr17:21214131-21214359 | Common:2; Rare:103 | ||||
chr17:27294002-27294122 | Common:1; Rare:48 | ||||
chr17:27294269-27294384 | Common:1; Rare:36 | ||||
chr17:28318909-28319250 | Common:3; Rare:119 | ||||
chr17:28335354-28335832 | Common:1; Rare:114 | ||||
chr17:28357410-28357667 | Common:6; Rare:126 | ||||
chr17:28370263-28370348 | Rare:8 |