chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7110912619110912620GT48GENIChomozygous145634966
7110913347110913348GC41GENIChomozygous143365537
7110913887110913888CT38GENIChomozygous145634967
7110914301110914302C12GENIChomozygous145610073
7110914403110914404CT21GENIChomozygous145634968
7110916366110916367GA54GENIChomozygous145634969
7110916882110916883CT43GENIChomozygous138181969
7110918762110918763AG29GENIChomozygous145634970
7110919218110919219AG38GENIChomozygous138181970
7110919572110919573CT36GENIChomozygous145634971
7110920457110920458CT38GENIChomozygous145634972
7110920909110920910C37GENIChomozygous145610074
7110921662110921663GA56GENIChomozygous145634973
7110922710110922710G34GENIChomozygous145610075
7110923120110923121GA41GENIChomozygous143365553
7110923515110923516AG47GENIChomozygous143365554
7110923736110923737CG41GENIChomozygous143365555
7110923738110923739AT41GENIChomozygous143365556
7110914371110914372C18GENICheterozygous403617334
7110914371110914372CT18GENIChomozygous403617335