chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3139688834139688835TG18GENIChomozygous637256107
3139688855139688856G-11GENIChomozygous749251353
3139688857139688858CA10GENIChomozygous637256108
3139688875139688876T-10GENIChomozygous749251354
3139688879139688880CA10GENIChomozygous637256109
3139688880139688881AC11GENIChomozygous637256110
3139689319139689320GC30GENIChomozygous637256111
3139690392139690393AT12GENICpossibly homozygous637256112
3139692494139692507AAAAAAAAAAAAA-------------18GENIChomozygous749251355
3139693174139693175GA18GENIChomozygous637256113
3139696829139696830TC25GENIChomozygous637256114
3139697771139697772GA18GENIChomozygous637256115
3139701561139701562CT24GENIChomozygous637256116
3139703025139703026TTA14GENICpossibly homozygous749251356
3139703733139703734AG30GENIChomozygous637256117
3139704057139704058GA24GENIChomozygous637256118
3139704175139704176AACGTGATTGGCAGCCACTGGAGTTC32GENIChomozygous749251357
3139706461139706472CCCAAACAAAC-----------6GENICheterozygous749251358
3139708106139708107CA34GENIChomozygous637256119
3139710315139710317AC--8GENICheterozygous749251359
3139712174139712175AAGTGTGTGT13GENICpossibly homozygous749251361
3139715674139715675G-13GENIChomozygous749251362
3139715677139715678G-14GENIChomozygous749251363
3139715684139715685TTA15GENIChomozygous749251364
3139715737139715755TCTCTCTCTCTCTCTCTC------------------11GENICheterozygous749251365
3139715739139715755TCTCTCTCTCTCTCTC----------------11GENICheterozygous749251366
3139717616139717617CT29GENIChomozygous637256120