Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:15699620-15699778 | Common:1; Rare:46 | ||||
chr17:15999620-16000028 | Common:3; Rare:174; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
chr17:16040440-16040571 | Rare:24 | ||||
chr17:16047007-16047372 | Common:1; Rare:62 | ||||
chr17:16217115-16217240 | Rare:37; Clinvar:1 | ||||
chr17:17591657-17591889 | Common:1; Rare:65 | ||||
chr17:18039091-18039387 | Common:3; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
chr17:18087740-18088026 | Rare:74 | ||||
chr17:18253319-18253682 | Rare:131 | ||||
chr17:18254554-18254823 | Rare:95 | ||||
chr17:18314898-18315331 | Common:1; Rare:121 | ||||
chr17:18781010-18781305 | Common:6; Rare:78 | ||||
chr17:19377622-19377773 | Common:2; Rare:38 | ||||
chr17:19377902-19378043 | Common:1; Rare:32 | ||||
chr17:19378162-19378537 | Common:2; Rare:92 |