Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:77798344-77798916 | Common:1; Rare:139 | ||||
chr7:79452747-79452882 | Rare:26 | ||||
chr7:79453534-79453772 | Common:1; Rare:58 | ||||
chr7:79453789-79454117 | Common:2; Rare:78 | ||||
chr7:87152300-87152468 | Common:1; Rare:52 | ||||
chr7:87345461-87345701 | Common:4; Rare:81 | ||||
chr7:87876342-87876657 | Common:1; Rare:138 | ||||
chr7:90346319-90346742 | Common:4; Rare:132 | ||||
chr7:91880677-91880823 | Common:2; Rare:39 | ||||
chr7:91940818-91940989 | Common:3; Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
chr7:92134364-92134553 | Rare:55 | ||||
chr7:92134709-92134890 | Common:3; Rare:54 | ||||
chr7:92245842-92246265 | Common:5; Rare:108; Clinvar:4; Clinvar (benign):5 | ||||
chr7:92528427-92528816 | Common:3; Rare:125; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr7:93232201-93232379 | Common:2; Rare:32 |