Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:35814983-35815294 | Rare:79 | ||||
chr9:36258409-36258622 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
chr9:37904079-37904462 | Common:3; Rare:124 | ||||
chr9:68356354-68356628 | Common:7; Rare:47 | ||||
chr9:70258823-70259075 | Common:4; Rare:119 | ||||
chr9:71911192-71911667 | Common:3; Rare:132 | ||||
chr9:75088140-75088591 | Common:3; Rare:157 | ||||
chr9:75890527-75890680 | Common:2; Rare:48 | ||||
chr9:83707675-83708292 | Common:5; Rare:201 | ||||
chr9:83980164-83980359 | Rare:68 | ||||
chr9:83980533-83980803 | Common:3; Rare:108 | ||||
chr9:86354379-86354638 | Common:1; Rare:115 | ||||
chr9:87725954-87726230 | Common:5; Rare:87 | ||||
chr9:88388214-88388504 | Common:1; Rare:127 | ||||
chr9:89310910-89311205 | Common:2; Rare:86 |