Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:186567291-186567400 | Common:3; Rare:31 | ||||
chr3:186806438-186806541 | Rare:32 | ||||
chr3:188153624-188153881 | Common:1; Rare:47 | ||||
chr3:189631096-189631202 | Common:1; Rare:17 | ||||
chr3:193593109-193593261 | Rare:44 | ||||
chr3:194135877-194136150 | Rare:66 | ||||
chr3:196318168-196318350 | Common:1; Rare:77 | ||||
chr3:196942519-196942673 | Common:1; Rare:65 | ||||
chr3:197736851-197737089 | Common:3; Rare:69 | ||||
chr3:197749759-197749962 | Common:1; Rare:76 | ||||
chr3:197949885-197950240 | Common:4; Rare:107; Clinvar (benign):2 | ||||
chr3:197959979-197960242 | Common:1; Rare:92 | ||||
chr4:499149-499279 | Common:2; Rare:39 | ||||
chr4:674253-674553 | Common:1; Rare:138 | ||||
chr4:932290-932460 | Common:2; Rare:68 |