chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4144302018144302019GA32GENIChomozygous112869756
4144302264144302265CT35GENIChomozygous112869757
4144302566144302567CT17GENIChomozygous112869758
4144302862144302863GT34GENIChomozygous112869759
4144303022144303023AG22GENIChomozygous112869760
4144303904144303905CT28GENIChomozygous112869761
4144304135144304136CT40GENIChomozygous112869762
4144304606144304607GA22GENIChomozygous112869763
4144304831144304832CT21GENIChomozygous112869764
4144304959144304960TC21GENIChomozygous112869765
4144305244144305245CT26GENIChomozygous112869766
4144305432144305433AC29GENIChomozygous112869767
4144307875144307876CT44GENIChomozygous112869768
4144309237144309238AG34GENIChomozygous112869772
4144308038144308039TG32GENIChomozygous112869769
4144308342144308343CT37GENIChomozygous112869770
4144308492144308493TC49GENIChomozygous112869771
4144309635144309636CA26GENIChomozygous112869773
4144311340144311341GT41GENIChomozygous112869774
4144311865144311866AG31GENIChomozygous112869775
4144317480144317481CT40GENIChomozygous112869777
4144317828144317829CT37GENIChomozygous112869778
4144319979144319980AG41GENIChomozygous112869779
4144320680144320681AG32GENIChomozygous112869780
4144321044144321045GA25GENIChomozygous112869781
4144322067144322068CT23GENIChomozygous112869782