Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:4538394-4538607 | Common:2; Rare:73 | ||||
chr16:4614886-4615063 | Common:1; Rare:48 | ||||
chr16:4693476-4693763 | Common:3; Rare:130 | ||||
chr16:4734199-4734534 | Common:1; Rare:109 | ||||
chr16:4767146-4767349 | Common:1; Rare:65 | ||||
chr16:4847226-4847414 | Common:1; Rare:86 | ||||
chr16:5097735-5098007 | Common:4; Rare:100 | ||||
chr16:8621620-8621710 | Common:1; Rare:36 | ||||
chr16:8674391-8674668 | Common:1; Rare:101; Clinvar:2 | ||||
chr16:8797621-8797866 | Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
chr16:10385920-10386099 | Rare:69 | ||||
chr16:10580561-10580853 | Common:2; Rare:98 | ||||
chr16:10743750-10743893 | Rare:55 | ||||
chr16:10944327-10944627 | Common:1; Rare:91 | ||||
chr16:11851517-11851635 | Rare:57 |