chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159951043159951044AG29GENIChomozygous114073647
5159951491159951492CT31GENIChomozygous114073648
5159951625159951626TC44GENIChomozygous114073649
5159952171159952172GA40GENIChomozygous114073650
5159952281159952282TC40GENIChomozygous114073651
5159953517159953518AG43GENIChomozygous114073652
5159953690159953691TC37GENIChomozygous114073653
5159955099159955100CT37GENIChomozygous114073654
5159955717159955718AT41GENIChomozygous114073655
5159956462159956463CA31GENIChomozygous114073656
5159956732159956733TC27GENIChomozygous114073657
5159956778159956779GC17GENIChomozygous114073658
5159956970159956971GA29GENIChomozygous114073659
5159957365159957366GA32GENIChomozygous114073660
5159957394159957395AG30GENIChomozygous114073661
5159957631159957632TC15GENIChomozygous114073662
5159957696159957697CT25GENIChomozygous114073663
5159957809159957810CA23GENIChomozygous114073664
5159957994159957995CT19GENIChomozygous114073665
5159958391159958392GA25GENIChomozygous114073666
5159958410159958411TC24GENIChomozygous114073667
5159958421159958422TC30GENIChomozygous114073668
5159958513159958514AG41GENIChomozygous114073669
5159958709159958710AC42GENIChomozygous114073670
5159958718159958719CT40GENIChomozygous114073671
5159958917159958918GA39GENIChomozygous114073672
5159958963159958964AG35GENIChomozygous114073673
5159959363159959364GA31GENIChomozygous114073674
5159959553159959554GA42GENIChomozygous114073675
5159959629159959630GA44GENIChomozygous114073676
5159963959159963960TG26GENIChomozygous114073677
5159966137159966138AG41GENIChomozygous114073678
5159966862159966863GA34GENICheterozygous114452618
5159966931159966932GA43GENICpossibly homozygous114073679
5159968562159968563CT25GENIChomozygous114073680