chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2246924674246924675A-12GENIChomozygous59487675
2246925670246925671C-32GENIChomozygous59487679
2246926128246926129AG22GENIChomozygous59487681
2246926531246926532TC27GENIChomozygous59487683
2246927747246927748TC18GENIChomozygous59487685
2246928068246928069GA16GENIChomozygous59487687
2246929503246929504GC29GENIChomozygous59487689
2246930632246930633A-9GENICpossibly homozygous60524540
2246931141246931142TC26GENIChomozygous59487691
2246931451246931455ACAT----5GENIChomozygous61976816
2246933023246933024GA12GENIChomozygous59487697
2246934074246934075AACACT25GENIChomozygous59487699
2246935618246935621CCC---7GENIChomozygous59487701
2246935677246935678CG10GENIChomozygous60463243
2246936606246936607CCT20GENIChomozygous59487703
2246939070246939071TG33GENIChomozygous59487705
2246939444246939445TTA18GENIChomozygous59487706
2246939884246939885G-8GENICheterozygous59487708
2246939916246939917GGA2GENIChomozygous59487710