chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
62715461527154616A35GENIChomozygous133157865
62716755527167556GC59GENIChomozygous115449132
62716899927168999C68GENIChomozygous131660537
62716918727169188CT58GENIChomozygous115494165
62716962227169623TC68GENIChomozygous115449138
62716980927169810CA66GENICpossibly homozygous115494167
62716984527169848GGG67GENIChomozygous131660538
62717116427171165CA73GENIChomozygous115494171
62717321727173218TC48GENIChomozygous115449142
62717346727173468CG24GENICheterozygous132979073
62717412227174123CA45GENIChomozygous115449146
62717490527174906GA60GENIChomozygous115449148
62717548227175483CT58GENIChomozygous115449150
62717629527176296GA58GENICpossibly homozygous115449152
62717761527177616GA58GENIChomozygous115449156
62717773327177734TC65GENIChomozygous115449158
62718050027180501GA27GENIChomozygous115449160
62718160827181614TCTGTT28GENIChomozygous132850804
62718456327184564GC58GENIChomozygous115449170
62718164127181642GC34GENIChomozygous115449164
62718213027182131GT41GENIChomozygous115449166
62718333527183336CG58GENIChomozygous115449168
62718484227184843CT43GENIChomozygous115449172
62718494927184950CA42GENIChomozygous115449174
62718586627185866C52GENIChomozygous131660540
62718720727187214GTGAGAG48GENIChomozygous132850805
62718742627187427AC56GENIChomozygous115449176
62718903427189040TCTCGT3GENIChomozygous133157867
62718917027189171TC58GENIChomozygous115449178
62718981927189820CG35GENIChomozygous115449180