Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:93187632-93187752 | Rare:22 | ||||
chr9:96484248-96484468 | Common:1; Rare:28 | ||||
chr9:97687241-97687397 | Common:1; Rare:36; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr9:113256003-113256271 | Common:1; Rare:56 | ||||
chr9:123339985-123340146 | Rare:38 | ||||
chr9:125537994-125538283 | Rare:47 | ||||
chr9:127818349-127818547 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):4 | ||||
chr9:127819621-127819708 | Rare:29; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr9:128630168-128630342 | Common:3; Rare:43; Clinvar (benign):3 | ||||
chr9:130712960-130713053 | Common:1; Rare:29 | ||||
chr9:131373437-131373671 | Common:1; Rare:55 | ||||
chr9:131483488-131483714 | Common:1; Rare:42 | ||||
chr9:136669675-136669932 | Common:1; Rare:71 | ||||
chr9:136839444-136839764 | Common:1; Rare:118 | ||||
chr9:136847916-136848069 | Rare:29 |