chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103283960532839606GA17GENICheterozygous51396652
103283996132839962GA17GENICheterozygous51396654
103284037732840378CG7GENICheterozygous53558068
103284037832840379TTGTG7GENICheterozygous53558069
103284037932840380CCG7GENICheterozygous53558070
103284038132840382CG7GENICheterozygous52240976
103284206432842065AG22GENICheterozygous53558071
103284236932842370G-15GENIChomozygous51396658
103284237732842378C-15GENIChomozygous51396659
103284245232842453TG23GENICheterozygous51396660
103284281432842815TA12GENICheterozygous53558072
103284306932843070CT19GENICheterozygous53558073
103284343332843434CCAATA16GENIChomozygous51396663
103284372732843728TC19GENICheterozygous51396666
103284417132844172AG21GENICheterozygous51396668
103284553032845531CT10GENICheterozygous51396673
103284659432846595GA9GENICheterozygous51839365
103284792032847921CT6GENICheterozygous53558074
103285204532852046AG22GENICheterozygous51396681
103284839432848395GC8GENICheterozygous52136563
103285972032859721AT11GENICheterozygous53558075
103286052332860524GT11GENICheterozygous51396695
103286388232863883AG16GENICheterozygous51396706
103286450632864507AG16GENICheterozygous51396708
103286470632864709TTT---11GENICheterozygous51396709
103286521832865219TC14GENICheterozygous53558076