chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108877114108877115CT42GENIChomozygous529758546
10108877194108877195CT23GENIChomozygous529758547
10108877595108877596TG20GENIChomozygous529758548
10108877657108877658AG27GENIChomozygous529758549
10108877702108877703AT26GENIChomozygous529758550
10108877811108877812GA29GENICheterozygous532416255
10108877927108877928CT14GENICheterozygous529758551
10108878538108878539CCTT12GENIChomozygous694438122
10108878562108878563CCTT10GENIChomozygous694438124
10108878644108878645TC29GENICpossibly homozygous529758552