chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7110912619110912620GT27GENIChomozygous145634966
7110913347110913348GC29GENIChomozygous143365537
7110913887110913888CT40GENIChomozygous145634967
7110914403110914404CT26GENICheterozygous145634968
7110916366110916367GA33GENIChomozygous145634969
7110916882110916883CT32GENIChomozygous138181969
7110918762110918763AG25GENIChomozygous145634970
7110919218110919219AG31GENIChomozygous138181970
7110919572110919573CT18GENIChomozygous145634971
7110920457110920458CT25GENIChomozygous145634972
7110921662110921663GA34GENICpossibly homozygous145634973
7110923120110923121GA24GENIChomozygous143365553
7110923515110923516AG31GENIChomozygous143365554
7110923736110923737CG26GENIChomozygous143365555
7110923738110923739AT26GENIChomozygous143365556
7110914301110914302C18GENIChomozygous145610073
7110920909110920910C20GENIChomozygous145610074
7110922710110922710G17GENIChomozygous145610075
7110914371110914372C31GENICheterozygous403617334
7110914371110914372CT31GENIChomozygous403617335