chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55778042157780422AG25GENIChomozygous113816228
55778151557781516TG24GENIChomozygous113816231
55778730557787306AG29GENIChomozygous113816249
55778840357788404AG28GENIChomozygous114205719
55778844357788444TC29GENIChomozygous113816251
55778857657788577AG26GENIChomozygous113816253
55779321557793216TC39GENIChomozygous114205720
55779382357793824GA16GENIChomozygous113816270
55779520757795208AC29GENIChomozygous114205722
55779565357795654TA15GENIChomozygous113816276
55780128557801286CT26GENIChomozygous113816300
55780259657802597TC19GENIChomozygous113816306
55780441657804417GC18GENIChomozygous114205724
55780462157804622CG20GENIChomozygous113816310
55780683257806833CG22GENIChomozygous114205725
55781281957812820GT9GENIChomozygous114205727
55781358357813584CG27GENIChomozygous114205728
55781555557815556GT24GENIChomozygous113816346
55781570157815702GC6GENIChomozygous118942472
55781571957815720CG12GENIChomozygous114330512
55781787857817879TC18GENIChomozygous114205731
55781908857819089CA19GENIChomozygous114205732
55782755457827555CT13GENIChomozygous114205734
55782826157828262AG27GENIChomozygous113816368
55782885957828860CT14GENIChomozygous114205735
55782922357829224GA13GENIChomozygous113816370
55783004057830041AT22GENIChomozygous113816372
55783175457831755CT18GENIChomozygous114205736
55783202157832022AG16GENIChomozygous113816376
55783544157835442CT31GENIChomozygous113816380
55783655357836554CT17GENIChomozygous113816388
55783655457836555TG16GENIChomozygous114117734
55784217257842173GA23GENICpossibly homozygous114205738
55784402957844030AT16GENIChomozygous114205739
55784499157844992TA13GENICheterozygous114205740
55784543857845439AT14GENIChomozygous114205741
55781571357815714CG6GENIChomozygous119012006
55781571657815717CG10GENIChomozygous119012007