chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91671139016711391TC25GENICheterozygous818026030
91671139416711395CT26GENICheterozygous818026031
91671143116711432TC27GENICheterozygous818026032
91671144116711442GA28GENICheterozygous818026033
91671145916711460GA28GENICheterozygous818026034
91671147816711479GA26GENICheterozygous818026035
91671149816711499CT29GENICheterozygous818026036
91671150216711503AG29GENICheterozygous818026037
91671152216711523CT23GENICheterozygous818026038
91671152316711524CT23GENICheterozygous818026039
91671182316711824CT23GENICheterozygous818026040
91671182816711829CT25GENICheterozygous818026041
91671184316711844CA23GENICheterozygous818026042
91671185616711857C-25GENICheterozygous818026043
91671185716711858AG27GENICheterozygous818026044
91671186416711865CT27GENICheterozygous818026045
91671188016711881CT24GENICheterozygous818026046
91671188216711883TC24GENICheterozygous818026047