chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140222794140222795TC17GENICpossibly homozygous69178729
7140222806140222807TC21GENICpossibly homozygous69178730
7140222833140222834AG21GENIChomozygous69178731
7140222851140222852TC27GENICheterozygous69178732
7140223570140223571AG7GENIChomozygous69178733
7140223642140223643CT26GENICpossibly homozygous69178734
7140223648140223649TA26GENICpossibly homozygous69178735
7140224339140224340CT24GENIChomozygous69178736
7140224801140224802TC25GENIChomozygous69178737
7140224857140224858GT32GENIChomozygous69178738
7140224940140224941TA27GENIChomozygous69178739
7140225035140225036GA29GENIChomozygous69178740
7140225377140225378TC15GENIChomozygous69178741
7140225383140225384CG15GENIChomozygous69178742
7140225588140225589TC33GENIChomozygous69178743
7140227280140227281GC23GENIChomozygous69178745