Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:67528698-67528883 | Rare:53 | ||||
chr16:67660228-67660364 | Rare:79; Clinvar:2; Clinvar (benign):2 | ||||
chr16:67666691-67666841 | Rare:30 | ||||
chr16:67806532-67806867 | Rare:65 | ||||
chr16:67935460-67935981 | Common:2; Rare:169 | ||||
chr16:67968565-67968717 | Common:1; Rare:63 | ||||
chr16:68023209-68023312 | Common:1; Rare:28 | ||||
chr16:68245161-68245410 | Common:1; Rare:74 | ||||
chr16:68291369-68291557 | Rare:39 | ||||
chr16:68310928-68311062 | Common:1; Rare:64 | ||||
chr16:68843469-68843620 | Rare:56 | ||||
chr16:69132537-69132671 | Rare:55 | ||||
chr16:69187019-69187164 | Rare:53 | ||||
chr16:69339548-69339801 | Rare:100; Clinvar (benign):1 | ||||
chr16:69726552-69726779 | Common:3; Rare:50 |