chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143553145835531459TC31GENIChomozygous113421886
143553335435533355AG25GENICheterozygous118782940
143553336435533365AG24GENICheterozygous118688012
143553491335534914TG26GENIChomozygous113421887
143553708335537084AC24GENICheterozygous118794767
143553916235539163CT40GENIChomozygous113421888
143553963735539638TC24GENIChomozygous113421889
143554066035540661GA9GENIChomozygous113672875
143554220535542206AG29GENIChomozygous113421890
143554267535542676CA10GENIChomozygous114043672
143554357635543577GA19GENIChomozygous113421891
143554423935544240AT18GENIChomozygous113421892
143554669135546692AG19GENIChomozygous113421893
143554687335546874TA4GENIChomozygous113421894
143554902735549028TG21GENIChomozygous113421895
143555014035550141AC16GENIChomozygous113421896
143555441735554418AG32GENICpossibly homozygous113585714
143555458335554584AG18GENIChomozygous113421897
143555586035555861CA11GENIChomozygous118688014
143555823035558231AG31GENIChomozygous113421898
143556366035563661GT19GENIChomozygous113421899
143556426635564267AT24GENIChomozygous113421900
143556566635565667TA22GENIChomozygous113421901
143556626535566266GA33GENIChomozygous113421902
143556667435566675CT8GENIChomozygous114043674
143556683135566832CT19GENIChomozygous113421903
143556798935567990TC29GENIChomozygous113421906
143556804935568050TC23GENIChomozygous113421907
143556877435568775GA41GENICheterozygous118688015
143556877835568779GA44GENICheterozygous118688016
143557013235570133GA34GENIChomozygous113421908
143557072935570730GA23GENIChomozygous113421909
143557160735571608AG22GENIChomozygous113421910
143557177735571778AT36GENIChomozygous113421911
143557298335572984AG35GENIChomozygous113421913
143557393535573936CA30GENIChomozygous113421914
143557438935574390GA12GENIChomozygous113818123
143557857635578577TG27GENIChomozygous113421915
143557987935579880TC15GENIChomozygous113421916
143558047635580477GA25GENIChomozygous113421917