Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:98255623-98255849 | Common:3; Rare:69 | ||||
chr9:98943473-98943578 | Rare:19 | ||||
chr9:99221898-99222364 | Common:2; Rare:187; Clinvar:2; Clinvar (benign):3 | ||||
chr9:99821585-99821889 | Rare:100 | ||||
chr9:99906570-99906712 | Rare:67 | ||||
chr9:100098964-100099314 | Common:3; Rare:99; Clinvar:2 | ||||
chr9:100352860-100353085 | Rare:81 | ||||
chr9:100427112-100427384 | Common:3; Rare:95 | ||||
chr9:101398565-101398910 | Common:1; Rare:118 | ||||
chr9:101487049-101487140 | Rare:29 | ||||
chr9:101487158-101487221 | Common:2; Rare:13 | ||||
chr9:104747554-104747782 | Common:1; Rare:66 | ||||
chr9:105447936-105448126 | Common:2; Rare:73 | ||||
chr9:105558009-105558184 | Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
chr9:106862973-106863172 | Rare:69 |