chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159951043159951044AG29GENIChomozygous114073647
5159951491159951492CT30GENICpossibly homozygous114073648
5159951625159951626TC18GENIChomozygous114073649
5159952171159952172GA18GENIChomozygous114073650
5159952281159952282TC37GENIChomozygous114073651
5159953517159953518AG32GENIChomozygous114073652
5159953690159953691TC26GENIChomozygous114073653
5159955099159955100CT31GENIChomozygous114073654
5159955717159955718AT34GENIChomozygous114073655
5159956462159956463CA31GENIChomozygous114073656
5159956732159956733TC30GENIChomozygous114073657
5159956778159956779GC25GENIChomozygous114073658
5159956970159956971GA24GENIChomozygous114073659
5159957365159957366GA40GENIChomozygous114073660
5159957394159957395AG34GENIChomozygous114073661
5159957631159957632TC18GENIChomozygous114073662
5159957696159957697CT29GENIChomozygous114073663
5159957809159957810CA21GENIChomozygous114073664
5159957994159957995CT22GENIChomozygous114073665
5159958391159958392GA13GENIChomozygous114073666
5159958410159958411TC16GENIChomozygous114073667
5159958421159958422TC16GENIChomozygous114073668
5159958513159958514AG21GENIChomozygous114073669
5159958688159958689TA19GENICheterozygous114160458
5159958709159958710AC19GENIChomozygous114073670
5159958718159958719CT17GENIChomozygous114073671
5159958917159958918GA13GENIChomozygous114073672
5159958963159958964AG26GENIChomozygous114073673
5159959363159959364GA30GENIChomozygous114073674
5159959553159959554GA26GENIChomozygous114073675
5159959629159959630GA16GENIChomozygous114073676
5159963959159963960TG24GENIChomozygous114073677
5159966137159966138AG34GENIChomozygous114073678
5159966862159966863GA27GENICpossibly homozygous114452618
5159966931159966932GA43GENICheterozygous114073679
5159968562159968563CT34GENICpossibly homozygous114073680