chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159808038159808039AC18GENICheterozygous55814280
5159808085159808086GT10GENICheterozygous55814281
5159808886159808887AG5GENICheterozygous55814284
5159817008159817009TC17GENICheterozygous55814309
5159817074159817075CT20GENICheterozygous55814310
5159817892159817893CT18GENICheterozygous55814316
5159817898159817899TC23GENICheterozygous55814317
5159827299159827300GA7GENICheterozygous55814331
5159828015159828016CT6GENICheterozygous55814332
5159829101159829102AG12GENICheterozygous55814333
5159829104159829105AC11GENICheterozygous55814334
5159829114159829115GT13GENICheterozygous55814335
5159829252159829253CG19GENICheterozygous55814336
5159829382159829383AG25GENICheterozygous55814337
5159829498159829499GA33GENICheterozygous55814338
5159829684159829685AG20GENICheterozygous55814339