Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:124861903-124862145 | Common:1; Rare:104 | ||||
chr9:125189725-125189829 | Rare:71 | ||||
chr9:125200421-125200590 | Common:1; Rare:64 | ||||
chr9:125241282-125241708 | Common:4; Rare:136 | ||||
chr9:125707137-125707349 | Common:2; Rare:68 | ||||
chr9:126804912-126805046 | Rare:45 | ||||
chr9:127451263-127451533 | Common:2; Rare:117 | ||||
chr9:127877661-127877791 | Rare:25 | ||||
chr9:128160046-128160391 | Common:2; Rare:85 | ||||
chr9:128275929-128276312 | Common:5; Rare:176 | ||||
chr9:128322410-128322486 | Rare:31 | ||||
chr9:128322739-128322880 | Common:2; Rare:65; Clinvar (benign):5 | ||||
chr9:128371193-128371399 | Rare:77 | ||||
chr9:128504616-128504793 | Rare:79; Clinvar:5 | ||||
chr9:128552398-128552593 | Rare:71; Clinvar:1 |