Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:30355219-30355434 | Common:1; Rare:76 | ||||
chr16:30504757-30504789 | Rare:4 | ||||
chr16:30534702-30535098 | Common:3; Rare:123 | ||||
chr16:30698480-30698639 | Common:1; Rare:61 | ||||
chr16:31033667-31033753 | Rare:19 | ||||
chr16:31074192-31074464 | Common:1; Rare:75 | ||||
chr16:31188853-31189225 | Common:2; Rare:79; Clinvar (pathogenic):1 | ||||
chr16:31190817-31191084 | Common:1; Rare:101; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr16:31202730-31202986 | Common:2; Rare:84 | ||||
chr16:31355008-31355271 | Common:2; Rare:69 | ||||
chr16:46689114-46689312 | Common:1; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
chr16:46973626-46973772 | Rare:70 | ||||
chr16:47460902-47460999 | Rare:38 | ||||
chr16:47461054-47461365 | Common:2; Rare:109; Clinvar (benign):2 | ||||
chr16:48365883-48366101 | Common:5; Rare:64 |