chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31257213912572140TG8GENIChomozygous57154977
31257283212572833GT29GENIChomozygous57154981
31257480212574803T-1GENIChomozygous57154985
31257569312575694TC17GENIChomozygous57154987
31257595912575960AG20GENIChomozygous57154989
31257628312576284GGT9GENICheterozygous57154993
31257741012577411TG20GENICpossibly homozygous57154997
31257956412579565AG21GENICpossibly homozygous57154999
31258214612582147CT28GENIChomozygous57155003
31258382912583830TC2GENIChomozygous57155007
31258415912584160AT17GENICpossibly homozygous57155011
31258475312584754GA12GENIChomozygous57155013
31259008312590084TC13GENICpossibly homozygous57155019
31259278812592789CA13GENICpossibly homozygous57155021
31259460812594609CT25GENIChomozygous57155025
31259471112594712AG10GENIChomozygous57155027
31259503912595040TC27GENIChomozygous57155029
31259529512595296TC23GENIChomozygous57155031
31259711912597120CT25GENICpossibly homozygous57155035
31259831212598313GT4GENIChomozygous57155037
31259851112598512TC14GENIChomozygous57155039
31259929612599297AG8GENIChomozygous57155041
31259986012599862AA--6GENIChomozygous57155049
31260219412602195CA20GENIChomozygous57155053
31260445212604453CCT1GENIChomozygous57155057
31261055112610552AG28GENIChomozygous57155061
31261158212611583TC26GENIChomozygous57155063
31261205912612060TC12GENIChomozygous57155065
31261229312612294AG5GENICheterozygous57155067
31261350212613503TG20GENICpossibly homozygous57155069
31261594312615944TG21GENICpossibly homozygous57155071
31261704912617050AG30GENICpossibly homozygous57155073
31261767612617677GA22GENIChomozygous57155075
31261786112617863GG--6GENICheterozygous58679126
31261926812619269CT12GENICpossibly homozygous57155081