chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124338947124338948GA21GENIChomozygous118360531
7124339161124339162GC26GENIChomozygous115865589
7124339558124339559CA26GENIChomozygous118360533
7124339853124339854CT28GENIChomozygous115865591
7124340122124340123GT31GENIChomozygous118360535
7124342549124342550CT28GENIChomozygous115865593
7124343070124343071TC22GENIChomozygous116226621
7124344290124344291CA25GENIChomozygous115865605
7124344579124344580CA28GENIChomozygous118360537
7124344725124344726AG37GENIChomozygous116226622
7124346017124346018AG14GENIChomozygous115865615
7124346439124346440GT34GENIChomozygous118360539
7124346535124346536GT36GENIChomozygous118360541
7124346977124346978TC27GENIChomozygous115865617
7124347350124347351CT29GENIChomozygous116226626
7124347675124347676GA25GENIChomozygous118360543
7124349089124349090TG25GENIChomozygous115865623
7124351265124351266AG16GENIChomozygous115865627
7124351551124351552CT19GENIChomozygous118360545
7124354044124354045TC17GENIChomozygous115865631
7124354543124354544TC28GENIChomozygous115865633
7124356412124356413AG28GENIChomozygous116226633
7124357590124357591CT26GENIChomozygous115865637
7124360268124360269GA29GENIChomozygous116226636
7124360930124360931GA25GENIChomozygous116226637
7124364485124364486GA23GENIChomozygous115865651
7124364503124364504CT23GENIChomozygous118360547
7124364758124364759CT27GENIChomozygous116226639
7124365980124365981CT31GENIChomozygous116226640
7124366145124366146TC29GENIChomozygous115865653
7124366572124366573GA25GENIChomozygous116226641
7124367287124367288GA27GENIChomozygous118360549