chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7144820586144820587GA20GENIChomozygous115945946
7144824467144824468TC33GENIChomozygous115945948
7144830091144830092TC17GENICpossibly homozygous115945949
7144830096144830097AC17GENICpossibly homozygous115945951
7144831797144831798AC19GENIChomozygous115945952
7144832359144832360GA42GENIChomozygous115945954
7144850296144850297CT37GENIChomozygous115945956
7144854579144854580GC29GENIChomozygous115945957
7144863039144863040AG21GENIChomozygous115945961
7144864312144864313TC36GENIChomozygous115945962