Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:4767126-4767330 | Common:1; Rare:67 | ||||
chr16:4833382-4833594 | Rare:44 | ||||
chr16:5033926-5033955 | Rare:8 | ||||
chr16:5071784-5071843 | Rare:26; Clinvar (benign):1 | ||||
chr16:5097728-5098007 | Common:4; Rare:102 | ||||
chr16:6483655-6483863 | Rare:71 | ||||
chr16:8797631-8797877 | Rare:96; Clinvar:2; Clinvar (benign):2 | ||||
chr16:8868977-8869255 | Common:4; Rare:123 | ||||
chr16:10743746-10743861 | Rare:43 | ||||
chr16:10818576-10818729 | Common:2; Rare:49 | ||||
chr16:11668248-11668522 | Common:3; Rare:120 | ||||
chr16:11851515-11851645 | Rare:62 | ||||
chr16:11915895-11916208 | Common:2; Rare:127 | ||||
chr16:11976648-11976766 | Rare:43 | ||||
chr16:12803827-12804013 | Common:3; Rare:49 |