Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:184000153-184000394 | Rare:41 | ||||
chr2:184000715-184000755 | Common:1; Rare:9 | ||||
chr2:184001160-184001228 | Rare:9 | ||||
chr2:184005162-184005450 | Rare:43 | ||||
chr2:190060675-190060914 | Rare:47 | ||||
chr2:196232104-196232147 | Rare:4 | ||||
chr2:197498780-197499051 | Common:3; Rare:79; Clinvar (benign):3 | ||||
chr2:199459312-199459505 | Common:1; Rare:51 | ||||
chr2:200065578-200065794 | Rare:31 | ||||
chr2:200147445-200147527 | Rare:14 | ||||
chr2:200148450-200148704 | Common:1; Rare:46 | ||||
chr2:200275420-200275621 | Common:1; Rare:32 | ||||
chr2:202376105-202376209 | Rare:56 | ||||
chr2:216083994-216084332 | Rare:68 | ||||
chr2:217277864-217278108 | Rare:49 |