Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:107193783-107193948 | Rare:32 | ||||
chr7:107659606-107659798 | Common:2; Rare:33 | ||||
chr7:107661603-107661899 | Rare:114; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):9 | ||||
chr7:107661934-107661998 | Common:1; Rare:15 | ||||
chr7:107662002-107662025 | Common:1; Rare:8 | ||||
chr7:107662115-107662171 | Rare:7 | ||||
chr7:107662175-107662233 | Rare:13 | ||||
chr7:107662243-107662397 | Rare:31 | ||||
chr7:107712017-107712348 | Rare:64 | ||||
chr7:107923539-107923841 | Rare:66 | ||||
chr7:107924336-107924659 | Common:3; Rare:63 | ||||
chr7:107972993-107973124 | Rare:35; Clinvar (benign):1 | ||||
chr7:112205572-112205679 | Rare:25 | ||||
chr7:112455794-112456025 | Common:4; Rare:51 | ||||
chr7:113118537-113118672 | Common:1; Rare:44 |