chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121108571121108572AG20GENIChomozygous118417994
7121108640121108641TA13GENIChomozygous118417995
7121109463121109464TG7GENIChomozygous115857999
7121111026121111027GA18GENIChomozygous115858001
7121111319121111320TG3GENICheterozygous116081980
7121111335121111336TG9GENICheterozygous115858003
7121112119121112120TC23GENIChomozygous115858005
7121113948121113949TC5GENIChomozygous115858007
7121115195121115196AG8GENIChomozygous115858009
7121115584121115585GA18GENIChomozygous118417996
7121115632121115633CT14GENIChomozygous118417997
7121115708121115709TC11GENIChomozygous115858011
7121115770121115771TC18GENIChomozygous118417998
7121115915121115916TG14GENIChomozygous115858013
7121118034121118035CT16GENIChomozygous118417999
7121119533121119534CT14GENICheterozygous115858024
7121119996121119997TC16GENIChomozygous118418000
7121120497121120498AG16GENICheterozygous115858026
7121123480121123481GA10GENIChomozygous118418001
7121125212121125213AG9GENIChomozygous118418002
7121125733121125734TC18GENIChomozygous118418003
7121116269121116270GA4GENICheterozygous126539141