Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:185937420-185937472 | Rare:12 | ||||
chr3:185937824-185938184 | Common:2; Rare:160 | ||||
chr3:186567268-186567431 | Common:3; Rare:49 | ||||
chr3:186783158-186783644 | Common:2; Rare:211 | ||||
chr3:186784100-186784477 | Common:2; Rare:156 | ||||
chr3:186806418-186806582 | Rare:59 | ||||
chr3:186930349-186930784 | Common:3; Rare:112 | ||||
chr3:188153630-188154224 | Common:1; Rare:135 | ||||
chr3:190322432-190322457 | Rare:5 | ||||
chr3:190513823-190514162 | Common:2; Rare:91 | ||||
chr3:191329225-191329711 | Common:4; Rare:147 | ||||
chr3:192917830-192918008 | Common:2; Rare:80 | ||||
chr3:193593048-193593404 | Rare:106; Clinvar:2; Clinvar (benign):2 | ||||
chr3:193593850-193594213 | Common:2; Rare:82 | ||||
chr3:194487003-194487165 | Common:3; Rare:73 |