chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48724204487242045CA19GENIChomozygous112767734
48724680087246801GA23GENIChomozygous112767736
48724924187249242GA18GENIChomozygous112767738
48724958287249583CT4GENIChomozygous112767740
48725043987250440AG45GENIChomozygous112767742
48725052087250521AG34GENIChomozygous112767744
48725156987251570GA12GENIChomozygous112767748
48725471987254720CG23GENIChomozygous112767772
48725490787254908GA27GENIChomozygous112767780
48725522187255222GA23GENIChomozygous112767782
48725575987255760GA22GENIChomozygous112767785
48725614887256149AG15GENICpossibly homozygous112767787
48725676687256767AT16GENIChomozygous112767789
48725809887258099TG26GENIChomozygous112767791
48725912987259130CT32GENIChomozygous113040604
48725963887259639GA26GENIChomozygous112767793
48726080087260801GA20GENIChomozygous112767795
48726116087261161TA15GENIChomozygous112767797
48726262887262629CA31GENIChomozygous112767799
48726320187263202AG27GENIChomozygous112767801
48726342687263427GC34GENIChomozygous112767803
48726360387263604AG32GENIChomozygous112767805
48726665887266659TC6GENIChomozygous113130365
48726666787266668AC4GENIChomozygous119358219
48727059487270595CA17GENIChomozygous112767809
48727266287272663AG22GENIChomozygous112767811
48727314587273146CA33GENIChomozygous112767813
48727650587276506TC24GENIChomozygous112767815
48727682987276830GA18GENIChomozygous112767817
48727698587276986TA27GENIChomozygous112767819
48727878887278789TA27GENIChomozygous112767833
48727932487279325AG24GENIChomozygous112767835
48727935987279360AG25GENIChomozygous112767837
48727954187279542CT21GENIChomozygous112767839
48727970287279703CG21GENIChomozygous112767841
48727973387279734AG26GENIChomozygous112767843
48727980387279804GA26GENIChomozygous112767845
48728006287280063CG21GENIChomozygous112767847
48728006587280066CT21GENIChomozygous112767849
48728023887280239GA28GENIChomozygous112767851
48728078687280787TG20GENIChomozygous112767854
48727680787276808AG17GENIChomozygous113517842