chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221713247221713248AT14GENIChomozygous108545112
1221714801221714802GC15GENIChomozygous108545113
1221715642221715643AG29GENIChomozygous108545115
1221715973221715974AG22GENIChomozygous108545117
1221716116221716117AG24GENIChomozygous108545119
1221716469221716470TC21GENIChomozygous108545121
1221716836221716837AG16GENIChomozygous108545123
1221722003221722004TC11GENIChomozygous108545129
1221722402221722403AG15GENIChomozygous108545131
1221723531221723532CT24GENIChomozygous108545135
1221723882221723883AG22GENIChomozygous108545137
1221724616221724617TG21GENIChomozygous108545139
1221724705221724706TG23GENIChomozygous108545141
1221726009221726010AG9GENIChomozygous108545143