Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:20651040-20651248 | Rare:62 | ||||
chr2:20823073-20823186 | Common:1; Rare:37 | ||||
chr2:23927066-23927325 | Common:3; Rare:90 | ||||
chr2:23940379-23940573 | Common:4; Rare:66 | ||||
chr2:24076204-24076541 | Rare:94 | ||||
chr2:24123272-24123510 | Common:1; Rare:63 | ||||
chr2:24360344-24360658 | Common:3; Rare:100 | ||||
chr2:24793067-24793161 | Rare:45 | ||||
chr2:24971907-24972153 | Common:1; Rare:79 | ||||
chr2:26033764-26034230 | Common:4; Rare:176 | ||||
chr2:26034260-26034732 | Common:4; Rare:112 | ||||
chr2:26195090-26195473 | Rare:114; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr2:26244528-26245017 | Common:2; Rare:172; Clinvar:7; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
chr2:26245134-26245179 | Rare:15 | ||||
chr2:26345789-26346193 | Common:1; Rare:120 |