chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4179262980179262981TC31GENIChomozygous798351585
4179272219179272220GA175GENICheterozygous798351586
4179272253179272254GA168GENICheterozygous798351587
4179272283179272284GA90GENICheterozygous798351588
4179275656179275657GT9GENIChomozygous798351589
4179275687179275688AC9GENIChomozygous798351590
4179277737179277738GC21GENIChomozygous798351591
4179277824179277825TA25GENIChomozygous798351592
4179287843179287844AT24GENICheterozygous798351593
4179302577179302578TG20GENIChomozygous798351594
4179302588179302589TG26GENIChomozygous798351595
4179316378179316379TA36GENICheterozygous798351596
4179316387179316388TC41GENICheterozygous798351597
4179316392179316393GA42GENICheterozygous798351598
4179316397179316398CT42GENICheterozygous798351599
4179316402179316403TC41GENICheterozygous798351600
4179316405179316406CT42GENICheterozygous798351601
4179316456179316457AG60GENICheterozygous798351602
4179316459179316460AG62GENICheterozygous798351603
4179316464179316465TC62GENICheterozygous798351604
4179316472179316473AC66GENICheterozygous798351605
4179316477179316478TC70GENICheterozygous798351606
4179316486179316487GA76GENICheterozygous798351607
4179316521179316522TC81GENICheterozygous798351608
4179316535179316536TC76GENICheterozygous798351609
4179316604179316605CA42GENICheterozygous798351610
4179316643179316644CA39GENICheterozygous798351611