chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123471185123471186GA37GENICpossibly homozygous115863186
7123471186123471187CA37GENICpossibly homozygous115863188
7123472140123472141CA23GENIChomozygous115863190
7123472656123472657CT61GENIChomozygous115863192
7123472928123472929TC45GENIChomozygous115863194
7123473032123473033TC71GENIChomozygous115863196
7123473697123473698TG43GENICpossibly homozygous115863198
7123473764123473765TG30GENICpossibly homozygous115863200
7123473768123473769TC32GENIChomozygous115863202
7123473811123473812TA22GENIChomozygous115863204
7123473830123473831AT25GENIChomozygous115863206
7123474907123474908TC54GENIChomozygous115863208
7123475618123475619TC46GENIChomozygous115863210