chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107608838276088383CT25GENIChomozygous52729189
107608838376088384CT25GENIChomozygous52729191
107608854276088543CT29GENIChomozygous51499984
107608863176088632GT29GENIChomozygous52729193
107608917976089180CA21GENIChomozygous52729195
107608985576089856AG23GENIChomozygous51499986
107609140076091401GA27GENIChomozygous51499987
107609182376091824TG18GENIChomozygous51499988
107609246576092467TT--8GENICpossibly homozygous51499989
107609373576093736AT26GENIChomozygous52729197
107609426776094268AATGTGTG22GENIChomozygous51499990
107609457776094578AG16GENIChomozygous51499991
107609670876096709CT15GENIChomozygous51499994
107609672176096722TTA15GENIChomozygous51499995
107609673976096740CT15GENIChomozygous52729199
107609674876096749AG18GENIChomozygous51499997
107609691876096919TC15GENIChomozygous52729201
107609698576096986TA19GENIChomozygous51499998
107609704876097049AG23GENIChomozygous52729203
107609739476097395AG23GENIChomozygous51499999
107609777876097779GA18GENIChomozygous52729205
107609672376096724GA16GENIChomozygous52386832