chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47051001170510012CT23GENIChomozygous143091168
47051126370511264A9GENIChomozygous403102991
47051126370511264AG9GENICheterozygous403102992
47051331770513318CG15GENIChomozygous137079398
47051424070514241GA21GENIChomozygous143091169
47051441370514414GT15GENIChomozygous143091170
47051491270514913CT22GENIChomozygous137079400
47051629470516295GA24GENIChomozygous137079403
47051644670516447CT18GENIChomozygous137079404
47051758370517584TC19GENIChomozygous137079406
47051775470517755CA27GENIChomozygous137079407
47051898870518989A21GENICheterozygous145440927
47051898870518989AT21GENIChomozygous154183579
47052152670521527TC24GENIChomozygous143091171
47052218570522191CGATCA17GENIChomozygous143050461
47052216870522168A16GENIChomozygous143050460
47051831870518323CAGTT23GENIChomozygous143050458
47052148470521485G19GENIChomozygous143050459
47052225570522256TC19GENIChomozygous143091172
47052229070522291GA16GENIChomozygous143091173
47052232970522330AG15GENIChomozygous143091174
47052235670522357GA17GENIChomozygous143091175
47052255270522553TC21GENIChomozygous143091176
47052282670522827AG14GENIChomozygous143091177