chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117781540877815409GT29GENICpossibly homozygous115911384
117781705477817055CT16GENICpossibly homozygous115911386
117782670977826710GA25GENICpossibly homozygous115911388
117782264077822641GA25GENIChomozygous116061131
117782837477828375TC32GENICpossibly homozygous115911390
117782861877828619GA21GENICpossibly homozygous115911392
117782884477828845AT32GENIChomozygous115911394
117782894377828944GT24GENICpossibly homozygous115911396
117782929377829294AG28GENIChomozygous115911398
117782936677829367AT29GENIChomozygous115911400
117782938577829386TC31GENIChomozygous115911402
117782945977829460AC40GENICpossibly homozygous115911404
117783029277830293CG23GENIChomozygous115911406