Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:101245000-101245182 | Common:1; Rare:75 | ||||
chr7:101321707-101321880 | Common:3; Rare:59 | ||||
chr7:102464846-102464965 | Common:1; Rare:49 | ||||
chr7:102478850-102479195 | Common:8; Rare:156 | ||||
chr7:104207959-104208112 | Common:3; Rare:70 | ||||
chr7:105013595-105013719 | Common:1; Rare:41 | ||||
chr7:105014097-105014220 | Common:1; Rare:55 | ||||
chr7:105532071-105532231 | Rare:43 | ||||
chr7:105876477-105876819 | Common:6; Rare:101 | ||||
chr7:106284904-106285276 | Common:2; Rare:145 | ||||
chr7:107563885-107563984 | Common:1; Rare:59; Clinvar (benign):1 | ||||
chr7:107744042-107744164 | Rare:42 | ||||
chr7:108526071-108526377 | Common:3; Rare:99 | ||||
chr7:108569554-108569938 | Common:2; Rare:137 | ||||
chr7:112206397-112206744 | Common:1; Rare:127 |