chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
79962624799626248AG11GENIChomozygous116217672
79962694199626942GA29GENIChomozygous118416109
79962961099629611GC24GENIChomozygous118416110
79963320599633206GA18GENIChomozygous118416111
79963322899633229TC14GENIChomozygous118416112
79963385099633851GA24GENIChomozygous118416113
79963014999630150GC19GENIChomozygous116408403
79963494799634948TC14GENIChomozygous116217679
79963551999635520AT26GENICpossibly homozygous118416114
79963580699635807TC30GENIChomozygous116217682
79963932799639328AG19GENIChomozygous116217684
79964076699640767GA30GENIChomozygous116217690
79964145499641455TC40GENIChomozygous116260631
79964295899642959GA27GENIChomozygous118416115
79964407199644072GT32GENIChomozygous118416116
79964426599644266AG37GENIChomozygous118416117
79964516299645163AC12GENIChomozygous116260635
79964477799644778TC25GENIChomozygous116260634
79964570999645710CA24GENIChomozygous118416118
79964575999645760CT26GENIChomozygous116408406
79964577299645773GA24GENIChomozygous118416119
79965196499651965CA28GENIChomozygous118416120
79965331599653316AG21GENIChomozygous116217693
79963911199639112TC34GENIChomozygous115785892
79965423399654234GA18GENIChomozygous115785894
79965568499655685CA17GENIChomozygous118416121
79966002499660025AC11GENIChomozygous115785910
79966080899660809CG19GENIChomozygous116217701
79966300799663008CT11GENIChomozygous118416122
79966340799663408TC19GENIChomozygous118416123
79966377299663773AG32GENIChomozygous116217702
79966478599664786GA35GENIChomozygous118416124
79966662199666622TG8GENIChomozygous118416125
79966746299667463AC25GENIChomozygous118416126
79966812099668121CT29GENIChomozygous118416127
79966936799669368GA25GENIChomozygous118416128
79967021699670217AC22GENIChomozygous116217705
79966004699660047AT13GENIChomozygous118331890
79967648799676488TC17GENIChomozygous116217713