chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101477078614770787AC27GENICheterozygous130683006
101477079014770791TC29GENICheterozygous130683007
101477390814773909AG64GENIChomozygous116496972
101477478414774785CT41GENIChomozygous116496974
101477529414775295TC59GENIChomozygous116496976
101477550014775501CT49GENIChomozygous116496978
101477746714777468AG48GENIChomozygous116496980
101477747214777473CA48GENIChomozygous116496982
101477754714777548AG56GENIChomozygous116496984
101477817314778174TC55GENIChomozygous116496986
101477861514778616GA61GENIChomozygous116496988
101477912514779126GA47GENIChomozygous116496990
101478040114780402GA52GENIChomozygous116496992
101478073714780738GT55GENIChomozygous116496994
101478110114781102CT51GENIChomozygous116496996
101478373714783738CT56GENIChomozygous116496998
101478491214784913CT29GENIChomozygous116497000
101478714214787143TC50GENIChomozygous116497002
101478720214787203TG51GENIChomozygous116497004
101478917414789175GC37GENIChomozygous117191308
101478118714781187TAACACAG24GENIChomozygous128790798
101477455514774555T59GENICpossibly homozygous128790796
101477746914777471AC48GENIChomozygous128790797