Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:16726849-16726910 | Common:1; Rare:13 | ||||
chr9:21559623-21559977 | Common:2; Rare:155 | ||||
chr9:35491665-35491767 | Rare:18 | ||||
chr9:40991995-40992381 | Common:7; Rare:28 | ||||
chr9:70413433-70413755 | Rare:96 | ||||
chr9:72305193-72305470 | Common:2; Rare:45 | ||||
chr9:92506437-92506672 | Rare:41 | ||||
chr9:107637722-107637798 | Rare:11 | ||||
chr9:115596342-115596686 | Common:5; Rare:50 | ||||
chr9:129488484-129488905 | Common:2; Rare:110 | ||||
chr9:129698608-129698765 | Rare:28 | ||||
chr9:134814875-134814966 | Rare:18; Clinvar:1; Clinvar (benign):1 | ||||
chr9:136400159-136400328 | Common:2; Rare:50 | ||||
chrM:403-561 | |||||
chrM:564-986 |