chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101796740217967403AAAAC7GENIChomozygous51628833
101796760517967606AATAACCTAGG1GENIChomozygous51335295
101796874617968747GA4GENIChomozygous51815629
101796932017969321TTAA4GENIChomozygous51815631
101796965617969657TC6GENIChomozygous51815633
101796970817969709AC10GENIChomozygous51815635
101797057017970571TTA6GENIChomozygous51335303
101797060617970607G-6GENIChomozygous51335304
101797061017970611TTA7GENIChomozygous51335305
101797061517970616A-6GENIChomozygous51335306
101797062017970621TTA5GENIChomozygous51335307
101797103517971036TC5GENIChomozygous51335312
101797139917971400AAT16GENICheterozygous51335315
101797140917971410CT29GENICpossibly homozygous51815637
101797185017971851CT17GENIChomozygous51815639
101797193617971937AG18GENICpossibly homozygous51335319
101797196317971964CCA5GENICheterozygous51815641
101797214517972147AC--14GENIChomozygous51335324
101797234217972343AC13GENIChomozygous51815643
101797259117972592TTA5GENIChomozygous51335329
101797282317972824TC17GENIChomozygous51335333
101797300217973003T-12GENIChomozygous51335334
101797441117974412GA19GENIChomozygous51815645
101797549417975495AG33GENIChomozygous51628842