Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:28357400-28357699 | Common:6; Rare:147; Clinvar (pathogenic):1 | ||||
chr17:28598994-28599159 | Common:2; Rare:46 | ||||
chr17:28645106-28645338 | Common:1; Rare:88 | ||||
chr17:28661877-28661976 | Rare:40 | ||||
chr17:28662106-28662314 | Rare:85 | ||||
chr17:28719655-28720046 | Common:1; Rare:112 | ||||
chr17:28720558-28720889 | Rare:127 | ||||
chr17:28728721-28728784 | Rare:19 | ||||
chr17:28812405-28812503 | Rare:27 | ||||
chr17:28842724-28842867 | Rare:53 | ||||
chr17:28854981-28855041 | Rare:18 | ||||
chr17:29293783-29293845 | Rare:19 | ||||
chr17:29294082-29294341 | Common:3; Rare:109 | ||||
chr17:29390249-29390363 | Common:1; Rare:36 | ||||
chr17:29568505-29568752 | Common:3; Rare:84 |