chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1171519407171519408TA17GENIChomozygous108378194
1171520231171520232TA20GENIChomozygous108378196
1171532558171532559CG10GENIChomozygous108378198
1171532833171532834AG17GENIChomozygous108378200
1171535305171535306TA7GENIChomozygous108378202
1171539016171539017AG23GENIChomozygous108378204
1171541444171541445AG15GENICheterozygous108378206
1171541685171541686CT13GENIChomozygous108378212
1171545349171545350GC23GENIChomozygous108378215
1171545383171545384GA18GENIChomozygous108378217
1171546974171546975AT15GENIChomozygous108378219
1171549137171549138GA16GENIChomozygous108378221
1171549564171549565AG28GENIChomozygous108378223
1171549976171549977AG24GENIChomozygous108378225
1171550183171550184GA15GENIChomozygous108378227
1171550803171550804TC18GENIChomozygous108378229
1171552541171552542CT8GENIChomozygous108378231
1171560252171560253AC27GENICpossibly homozygous108378235
1171560936171560937GC14GENICheterozygous108378238
1171562616171562617CT17GENIChomozygous108959601
1171563071171563072TC22GENIChomozygous108378240