chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47051320670513214ACAGACAG15GENICpossibly homozygous145440926
47051321370513214GC16GENICheterozygous403817170
47051321370513214G16GENICpossibly homozygous403817171
47051324670513250AGAC25GENIChomozygous144657103
47051331770513318CG40GENIChomozygous137079398
47051424070514241GA47GENIChomozygous143091169
47051491270514913CT52GENIChomozygous137079400
47051629470516295GA53GENIChomozygous137079403
47051644670516447CT66GENIChomozygous137079404
47051758370517584TC43GENIChomozygous137079406
47051775470517755CA44GENIChomozygous137079407
47051898870518989A36GENIChomozygous145440927
47051898870518989AT36GENICheterozygous154183579
47052152670521527TC60GENIChomozygous143091171
47052218570522191CGATCA54GENIChomozygous143050461
47051633070516331GC55GENIChomozygous145471470
47051757770517578GA44GENIChomozygous145471471
47051831870518323CAGTT38GENIChomozygous143050458
47052148470521485G64GENIChomozygous143050459
47052216870522168A54GENIChomozygous143050460
47052225570522256TC45GENIChomozygous143091172
47052229070522291GA49GENIChomozygous143091173
47052232970522330AG48GENIChomozygous143091174
47052235670522357GA52GENIChomozygous143091175
47052255270522553TC54GENICpossibly homozygous143091176
47052282670522827AG51GENIChomozygous143091177