chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
73179219631792197TC55GENICheterozygous926039190
73179237131792372CT51GENICheterozygous926039191
73179269631792697GA27GENICheterozygous926039192
73179464031794641TA50GENICheterozygous926039193
73179634131796342AG18GENICheterozygous926039194
73179800231798003AG22GENICheterozygous926039195
73180507031805071GA59GENICheterozygous926039196
73181608331816084TC20GENICheterozygous926039197
73181614131816142TC12GENICheterozygous926039198
73182062931820630TC27GENICheterozygous926039199
73182675431826755CT11GENICheterozygous926039200
73183889031838891AG23GENICheterozygous926039201
73184028731840288AG25GENICheterozygous926039202
73184987331849874CT22GENICheterozygous926039203
73185110131851102AAG40GENICheterozygous926092710
73185185431851855AG19GENICheterozygous926039204
73186298931862996AAAAAAG-------25GENICheterozygous926092711
73186301031863011CT17GENICheterozygous926039205
73187005131870052AG16GENICheterozygous926039206
73187268431872685AT9GENICheterozygous926039207
73187287131872872TC26GENICheterozygous926039208