chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71260634412606345GA38INTERGENIChomozygous807913501
71260641612606417TC41GENICpossibly homozygous807913502
71260694712606948AT42GENICpossibly homozygous807913503
71260695712606958GA48GENICpossibly homozygous807913504
71260701712607018TG50GENICheterozygous807913505
71260702412607025CT47GENICheterozygous807913506
71260731612607317AG37GENIChomozygous807913507
71260735612607357GA28GENIChomozygous807913508
71260735712607358CA28GENIChomozygous807913509
71260742012607421CA42GENICpossibly homozygous807913510
71260785412607855TC48GENIChomozygous807913511
71260806112608062GC37GENIChomozygous807913512
71260844212608443GA50GENIChomozygous807913513
71260924012609241CG52GENICheterozygous807913514
71260937412609375GT36GENICpossibly homozygous807913515
71260939412609395CT44GENICpossibly homozygous807913516
71260971312609714TC46INTERGENIChomozygous807913517