chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6108124565108124566GC57GENIChomozygous115150790
6108124574108124575CT56GENIChomozygous115150791
6108124704108124705GA36GENIChomozygous115150792
6108124921108124922AG59GENIChomozygous115150793
6108125652108125653AT45GENIChomozygous115150794
6108125807108125808AC52GENIChomozygous115150795
6108128022108128023GT45GENIChomozygous115150796
6108128626108128627AT64GENICpossibly homozygous115150797
6108130165108130166AG47GENIChomozygous115150798
6108133913108133914AG34GENIChomozygous115150800
6108135938108135939CT33GENIChomozygous115150802
6108139056108139057CT50GENIChomozygous115150804
6108140173108140174TA52GENIChomozygous115472304
6108140305108140306GC58GENIChomozygous115472306
6108143888108143889AT23GENICheterozygous115504200
6108144351108144352CT47GENIChomozygous115150806
6108144775108144776GA47GENIChomozygous115150807
6108145402108145403CG50GENIChomozygous115150810
6108146215108146216TA46GENICpossibly homozygous115150811
6108146856108146857GC38GENICpossibly homozygous115150812
6108147187108147188CT39GENIChomozygous115150813
6108147752108147753TA43GENICpossibly homozygous115150814
6108147990108147991AG48GENICpossibly homozygous115150815
6108148146108148147GT56GENIChomozygous115150816
6108148163108148164TC53GENIChomozygous115150817
6108148748108148749GA2GENIChomozygous115150818
6108149078108149079TC44GENICpossibly homozygous115150819
6108149185108149186AT42GENIChomozygous115150820
6108149298108149299AG45GENIChomozygous115150821
6108149403108149404CT35GENIChomozygous115150822
6108149409108149410CA35GENIChomozygous115150823
6108149458108149459TA29GENIChomozygous115150824
6108149495108149496CT25GENIChomozygous115223286