Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:98943681-98944003 | Common:4; Rare:97 | ||||
chr9:99906575-99906694 | Rare:61 | ||||
chr9:100098958-100099323 | Common:3; Rare:105; Clinvar:2 | ||||
chr9:100352860-100353094 | Rare:86 | ||||
chr9:101398587-101398902 | Common:1; Rare:101 | ||||
chr9:104093985-104094345 | Common:3; Rare:87 | ||||
chr9:104747644-104747799 | Common:1; Rare:48 | ||||
chr9:104764057-104764207 | Common:2; Rare:33 | ||||
chr9:105447950-105448153 | Common:2; Rare:76 | ||||
chr9:105558016-105558176 | Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
chr9:105694406-105694629 | Common:3; Rare:99 | ||||
chr9:106862980-106863180 | Rare:69 | ||||
chr9:108934074-108934477 | Common:7; Rare:161; Clinvar:2; Clinvar (benign):2 | ||||
chr9:110125358-110125542 | Rare:38 | ||||
chr9:110256425-110256684 | Common:2; Rare:94 |