Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:34302981-34303393 | Common:1; Rare:158; Clinvar:3; Clinvar (benign):2 | ||||
chr20:34516265-34516460 | Common:3; Rare:81 | ||||
chr20:34558552-34558767 | Common:1; Rare:59 | ||||
chr20:34677086-34677258 | Rare:46 | ||||
chr20:34955725-34955922 | Common:1; Rare:75; Clinvar:3; Clinvar (benign):3 | ||||
chr20:35172029-35172184 | Rare:41 | ||||
chr20:35284552-35284826 | Common:2; Rare:70 | ||||
chr20:35664855-35665015 | Common:1; Rare:43 | ||||
chr20:35699284-35699473 | Rare:67; Clinvar (benign):3 | ||||
chr20:35742153-35742636 | Common:5; Rare:148 | ||||
chr20:35771784-35772077 | Common:2; Rare:89 | ||||
chr20:36461264-36461502 | Common:1; Rare:67 | ||||
chr20:36541296-36541588 | Common:3; Rare:82 | ||||
chr20:36573388-36573616 | Rare:96 | ||||
chr20:36951436-36951466 | Rare:5; Clinvar (benign):1 |