Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:107563888-107564021 | Common:2; Rare:79; Clinvar (benign):3 | ||||
chr7:107580144-107580294 | Common:2; Rare:61 | ||||
chr7:107744018-107744171 | Rare:46 | ||||
chr7:108003097-108003525 | Common:5; Rare:127 | ||||
chr7:108526095-108526524 | Common:5; Rare:136 | ||||
chr7:108569535-108570056 | Common:3; Rare:185 | ||||
chr7:112206391-112206762 | Common:1; Rare:132 | ||||
chr7:112450272-112450474 | Common:4; Rare:66 | ||||
chr7:116499521-116499790 | Common:3; Rare:92 | ||||
chr7:116525660-116525780 | Rare:30 | ||||
chr7:118183965-118184209 | Common:2; Rare:95 | ||||
chr7:122144207-122144452 | Common:1; Rare:54 | ||||
chr7:123748899-123749229 | Common:3; Rare:115 | ||||
chr7:124929789-124929929 | Common:3; Rare:46 | ||||
chr7:127588268-127588530 | Rare:104 |