Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:98943469-98943578 | Rare:19 | ||||
chr9:99221916-99222357 | Common:2; Rare:172; Clinvar:2; Clinvar (benign):2 | ||||
chr9:99821717-99822001 | Rare:74 | ||||
chr9:99906570-99906717 | Rare:68 | ||||
chr9:100098974-100099349 | Common:3; Rare:106; Clinvar:2; Clinvar (benign):1 | ||||
chr9:100352858-100353078 | Rare:77 | ||||
chr9:101398580-101398919 | Common:1; Rare:112 | ||||
chr9:104093985-104094312 | Common:3; Rare:77 | ||||
chr9:104747547-104747757 | Rare:53 | ||||
chr9:104764158-104764193 | Rare:8 | ||||
chr9:104927941-104927990 | Rare:11; Clinvar:4 | ||||
chr9:105447950-105448144 | Common:2; Rare:70 | ||||
chr9:105558039-105558165 | Rare:41; Clinvar (benign):1 | ||||
chr9:106862979-106863180 | Rare:69 | ||||
chr9:106863514-106863630 | Common:1; Rare:22 |