Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1827168-1827255 | Common:1; Rare:48 | ||||
chr16:1943117-1943494 | Common:1; Rare:119 | ||||
chr16:1964795-1965017 | Common:8; Rare:106 | ||||
chr16:1971883-1972105 | Common:3; Rare:63 | ||||
chr16:2047733-2048050 | Rare:158; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2429165-2429481 | Common:2; Rare:98 | ||||
chr16:2682367-2682548 | Rare:75 | ||||
chr16:2752581-2752713 | Common:1; Rare:54 | ||||
chr16:2758518-2758665 | Rare:47 | ||||
chr16:2777222-2777388 | Common:1; Rare:66 | ||||
chr16:3134841-3135064 | Common:2; Rare:53 | ||||
chr16:3305428-3305514 | Common:1; Rare:24 | ||||
chr16:3400967-3401256 | Common:6; Rare:108 | ||||
chr16:3443443-3443729 | Common:3; Rare:99 | ||||
chr16:3611575-3611806 | Rare:99 |