chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1249709849249709850CCAAAAAAA16GENICheterozygous765908818
1249709851249709853AA--16GENICpossibly homozygous765908817
1249711041249711042AG29GENIChomozygous664620754
1249711274249711275AC22GENIChomozygous664620755
1249712591249712592CCT22GENICpossibly homozygous765908819
1249714897249714898GT13GENIChomozygous664620756
1249715029249715030AG17GENIChomozygous664620757
1249716349249716350GGA17GENICpossibly homozygous765908821
1249716857249716858AC23GENIChomozygous664620758