chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3109692776109692777CA29GENIChomozygous57979103
3109694118109694119TG11GENIChomozygous57979106
3109694512109694513CT20GENICpossibly homozygous57979109
3109694559109694560AAT13GENIChomozygous57979112
3109695294109695298AAGA----4GENIChomozygous58689747
3109695309109695313GAAA----4GENIChomozygous58689748
3109695345109695349GAAG----33GENIChomozygous58689749
3109696609109696610AT26GENIChomozygous57979121
3109696610109696611TC26GENIChomozygous57979124
3109696714109696715GA35GENIChomozygous57979127
3109697143109697144CT16GENIChomozygous57979130
3109697405109697406AC20GENIChomozygous57979132