chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
183001589030015891CT50GENIChomozygous110319239
183008096630080967AG49GENICheterozygous130711993
183008114530081146GC44GENICheterozygous131760731
183008115630081157GA45GENICheterozygous129570026
183008119730081198AG54GENICheterozygous130475682
183008120430081205AT56GENICheterozygous129570029
183008121830081219TA56GENICheterozygous129570030
183008122130081222GT58GENICheterozygous129570031
183008122330081224TC58GENICheterozygous131958748
183008100030081001AG39GENICheterozygous133036026
183008138730081388GT35GENICheterozygous129570034
183008148030081481GA34GENICheterozygous129570040
183008151830081519TC34GENICheterozygous132511025
183008153130081532AT39GENICheterozygous130475683
183008153930081540TC40GENICheterozygous130475684
183008157630081577AT44GENICheterozygous130475685
183008416730084168CT44GENICheterozygous134891560
183008455230084553GT44GENICheterozygous134891561
183009678230096783AC19GENICheterozygous134315355
183012612130126122TC26GENICheterozygous133785507
183012612630126127AC27GENICheterozygous133785508
183012613030126131TC27GENICheterozygous133785509
183014021130140212TC42GENIChomozygous110319712
183016816130168162GA19GENICheterozygous134891562