Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:29032089-29032398 | Common:1; Rare:46 | ||||
chr17:29265250-29265266 | |||||
chr17:29930805-29930892 | Rare:11 | ||||
chr17:30600332-30600450 | Common:4; Rare:27 | ||||
chr17:30701314-30701340 | Rare:6 | ||||
chr17:30708199-30708433 | Rare:52 | ||||
chr17:30708780-30709033 | Common:2; Rare:84 | ||||
chr17:30731880-30732124 | Rare:75 | ||||
chr17:32228130-32228263 | Common:1; Rare:33 | ||||
chr17:32369401-32369714 | Common:1; Rare:77 | ||||
chr17:32774053-32774184 | Common:1; Rare:25 | ||||
chr17:33156217-33156359 | Common:2; Rare:16 | ||||
chr17:34156500-34156666 | Rare:43 | ||||
chr17:35001207-35001311 | Rare:33; Clinvar (benign):1 | ||||
chr17:35568281-35568470 | Common:1; Rare:29 |