Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:104207973-104208109 | Common:2; Rare:56 | ||||
chr7:105013588-105013687 | Common:1; Rare:36 | ||||
chr7:105014087-105014268 | Common:1; Rare:73 | ||||
chr7:105014428-105014529 | Rare:23 | ||||
chr7:105532078-105532244 | Common:1; Rare:43 | ||||
chr7:105876477-105876818 | Common:6; Rare:100 | ||||
chr7:106284892-106285256 | Common:2; Rare:140 | ||||
chr7:106285539-106285678 | Rare:33 | ||||
chr7:107563852-107564032 | Common:2; Rare:107; Clinvar:1; Clinvar (benign):4 | ||||
chr7:107580079-107580294 | Common:2; Rare:78 | ||||
chr7:107743614-107743801 | Common:3; Rare:70 | ||||
chr7:107744018-107744171 | Rare:46 | ||||
chr7:108003119-108003435 | Common:3; Rare:99 | ||||
chr7:108526071-108526379 | Common:4; Rare:101 | ||||
chr7:108569572-108570008 | Common:3; Rare:159 |