chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41795650717956508GT22GENIChomozygous112530643
41795722017957221CT19GENIChomozygous112530644
41795843017958431CT34GENIChomozygous112530646
41795856417958565AG19GENIChomozygous112530648
41796386017963861TG13GENIChomozygous112530670
41796271417962715TC15GENIChomozygous112530666
41796381517963816AG15GENIChomozygous112530668
41796411417964115GA14GENIChomozygous112530672
41796692017966921CT9GENIChomozygous112530674
41796803717968038AC13GENIChomozygous112530678
41796975217969753AG19GENIChomozygous112530684
41797076917970770TC22GENIChomozygous112530686
41797217017972171AG6GENIChomozygous112530688
41797305817973059AT25GENIChomozygous112530690
41797317817973179TC29GENIChomozygous112530692
41797487317974874AC19GENIChomozygous112530694
41797489117974892CT16GENIChomozygous112530696
41797512817975129AG18GENIChomozygous112530698
41797696017976961CT7GENIChomozygous112530700
41797849217978493CA18GENIChomozygous112530702
41798006917980070CT19GENIChomozygous112530710
41797954317979544AG23GENIChomozygous112530704
41797955417979555GA22GENIChomozygous112530706
41797958017979581TC18GENIChomozygous112530708
41798029517980296AG20GENIChomozygous112530712
41798071317980714AG30GENIChomozygous112530714
41798102917981030GA27GENIChomozygous112530716
41798120917981210AG32GENIChomozygous112530718
41798121617981217CA34GENIChomozygous112530720
41798182517981826GA28GENIChomozygous112530722
41798202117982022AC22GENIChomozygous112530724
41798219817982199AC21GENIChomozygous112530726
41798233617982337AG29GENIChomozygous112530728
41798235717982358CT25GENIChomozygous112530730
41798246317982464GA22GENIChomozygous112530732
41798248917982490AG25GENIChomozygous112530734
41798263717982638AG22GENIChomozygous112530736
41798274317982744TC19GENIChomozygous112530738
41798285417982855GA21GENIChomozygous112530740
41798292917982930GA25GENIChomozygous112530742
41798318017983181TC25GENIChomozygous112530744