Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:29929228-29929321 | Rare:10 | ||||
chr17:29929616-29929913 | Common:1; Rare:72 | ||||
chr17:29930130-29930309 | Rare:61 | ||||
chr17:30824579-30824851 | Common:3; Rare:108 | ||||
chr17:30906205-30906344 | Common:1; Rare:39 | ||||
chr17:31094595-31094736 | Rare:24 | ||||
chr17:31095110-31095312 | Rare:68; Clinvar:4; Clinvar (benign):1 | ||||
chr17:31901608-31901930 | Common:3; Rare:94 | ||||
chr17:31936741-31937081 | Rare:99 | ||||
chr17:32142327-32142723 | Common:8; Rare:154 | ||||
chr17:32342114-32342262 | Rare:44 | ||||
chr17:32349976-32350258 | Rare:134 | ||||
chr17:32486446-32486738 | Common:1; Rare:110 | ||||
chr17:32487064-32487161 | Rare:26 | ||||
chr17:32876615-32876780 | Rare:59 |