chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4208492701208492702G-10GENICheterozygous58675161
4208492833208492834A-5GENICheterozygous58410592
4208492880208492881AG31GENIChomozygous57066601
4208495077208495078AG37GENIChomozygous57066602
4208497973208497974CCTTT18GENICheterozygous58724871
4208497975208497976T-18GENICheterozygous58369115
4208498471208498472TC17GENIChomozygous57066605
4208494215208494216CA39GENIChomozygous59172820
4208498546208498557AAAAAAAAAAA-----------7GENIChomozygous59172822
4208496186208496187GGT18GENICpossibly homozygous58600879
4208498924208498925TC18GENIChomozygous57066606
4208499666208499667CCT1GENIChomozygous58369117
4208500571208500572CCTT4GENICheterozygous58369119
4208501729208501730AG29GENIChomozygous58487496
4208504257208504258G-20GENIChomozygous59172824
4208504805208504806GC25GENIChomozygous58487498
4208504989208504990GA31GENIChomozygous59172826
4208505297208505298TC38GENIChomozygous57066610
4208510543208510544TC26GENIChomozygous57066613
4208511143208511147CTCT----31GENIChomozygous59172828
4208512907208512908TC30GENIChomozygous57066615
4208513452208513453AG36GENIChomozygous59172830
4208515226208515227AAT18GENICheterozygous58487501
4208515943208515944AG32GENIChomozygous57066616
4208517244208517245AC23GENIChomozygous59172832
4208519509208519510GGT14GENICpossibly homozygous58704313
4208519902208519903TC37GENIChomozygous58600907
4208522123208522124CT12GENIChomozygous59172834
4208522130208522133TTT---5GENIChomozygous59172836
4208522353208522354TC24GENIChomozygous57066620
4208523079208523080AG19GENIChomozygous57066621
4208529860208529861GC36GENIChomozygous57066623
4208530351208530353AA--19GENICheterozygous58369123
4208530352208530353A-19GENICheterozygous58487506
4208533095208533096GA27GENIChomozygous57066627
4208533489208533490TC46GENIChomozygous58600923