chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221713247221713248AT25GENIChomozygous108545112
1221714801221714802GC42GENIChomozygous108545113
1221715642221715643AG28GENICpossibly homozygous108545115
1221715973221715974AG39GENIChomozygous108545117
1221716116221716117AG33GENIChomozygous108545119
1221716469221716470TC28GENIChomozygous108545121
1221716836221716837AG39GENIChomozygous108545123
1221716968221716969AG40GENIChomozygous108545125
1221718958221718959CT25GENIChomozygous108545127
1221722402221722403AG17GENIChomozygous108545131
1221723531221723532CT40GENIChomozygous108545135
1221723882221723883AG45GENIChomozygous108545137
1221724616221724617TG38GENICpossibly homozygous108545139
1221724705221724706TG26GENICpossibly homozygous108545141
1221726009221726010AG35GENIChomozygous108545143