Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:98255647-98255915 | Common:3; Rare:86 | ||||
chr9:98943454-98943590 | Rare:22 | ||||
chr9:98943740-98943993 | Common:3; Rare:80 | ||||
chr9:99221940-99222329 | Common:2; Rare:139; Clinvar:2 | ||||
chr9:99906574-99906711 | Rare:66 | ||||
chr9:100098974-100099314 | Common:2; Rare:94; Clinvar:2 | ||||
chr9:100352866-100353094 | Rare:83 | ||||
chr9:101398564-101398887 | Common:1; Rare:114 | ||||
chr9:104093985-104094319 | Common:3; Rare:78 | ||||
chr9:104747643-104747802 | Common:1; Rare:51 | ||||
chr9:105447985-105448144 | Common:2; Rare:56 | ||||
chr9:105694232-105694627 | Common:6; Rare:130 | ||||
chr9:106862971-106863180 | Rare:72 | ||||
chr9:108934065-108934493 | Common:7; Rare:170; Clinvar:2; Clinvar (benign):2 | ||||
chr9:109498246-109498484 | Common:1; Rare:73 |