chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4144302018144302019GA52GENIChomozygous112869756
4144302264144302265CT55GENIChomozygous112869757
4144302566144302567CT61GENIChomozygous112869758
4144302862144302863GT49GENICpossibly homozygous112869759
4144303022144303023AG62GENICpossibly homozygous112869760
4144303904144303905CT52GENIChomozygous112869761
4144304135144304136CT68GENIChomozygous112869762
4144304606144304607GA62GENICpossibly homozygous112869763
4144304831144304832CT71GENIChomozygous112869764
4144304959144304960TC66GENIChomozygous112869765
4144305244144305245CT71GENIChomozygous112869766
4144305432144305433AC47GENIChomozygous112869767
4144307875144307876CT39GENIChomozygous112869768
4144308038144308039TG63GENIChomozygous112869769
4144308342144308343CT63GENICpossibly homozygous112869770
4144308492144308493TC65GENIChomozygous112869771
4144309237144309238AG42GENIChomozygous112869772
4144309635144309636CA60GENIChomozygous112869773
4144311340144311341GT50GENIChomozygous112869774
4144311865144311866AG41GENIChomozygous112869775
4144315279144315280GT54GENIChomozygous112869776
4144317480144317481CT58GENIChomozygous112869777
4144317828144317829CT40GENIChomozygous112869778
4144319979144319980AG63GENIChomozygous112869779
4144320680144320681AG47GENIChomozygous112869780
4144321044144321045GA64GENIChomozygous112869781
4144322067144322068CT62GENIChomozygous112869782