chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101477390814773909AG19GENIChomozygous116496972
101477455514774555T18GENIChomozygous128790796
101477478414774785CT17GENIChomozygous116496974
101477529414775295TC27GENIChomozygous116496976
101477550014775501CT16GENIChomozygous116496978
101477746714777468AG17GENIChomozygous116496980
101477746914777471AC17GENIChomozygous128790797
101477747214777473CA16GENIChomozygous116496982
101477754714777548AG17GENIChomozygous116496984
101477817314778174TC16GENIChomozygous116496986
101477861514778616GA24GENIChomozygous116496988
101477912514779126GA24GENIChomozygous116496990
101478040114780402GA18GENIChomozygous116496992
101478073714780738GT20GENIChomozygous116496994
101478110114781102CT16GENIChomozygous116496996
101478118714781187TAACACAG9GENIChomozygous128790798
101478373714783738CT20GENIChomozygous116496998
101478491214784913CT16GENIChomozygous116497000
101478714214787143TC19GENIChomozygous116497002
101478720214787203TG19GENIChomozygous116497004
101478917414789175GC16GENIChomozygous117191308