chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1171519407171519408TA42GENIChomozygous108378194
1171520231171520232TA46GENIChomozygous108378196
1171532558171532559CG31GENIChomozygous108378198
1171532820171532821CT54GENICheterozygous108755416
1171532833171532834AG51GENICpossibly homozygous108378200
1171535305171535306TA15GENIChomozygous108378202
1171539016171539017AG45GENIChomozygous108378204
1171541444171541445AG28GENICheterozygous108378206
1171541685171541686CT26GENIChomozygous108378212
1171545349171545350GC40GENIChomozygous108378215
1171545383171545384GA41GENIChomozygous108378217
1171546974171546975AT47GENIChomozygous108378219
1171549137171549138GA57GENIChomozygous108378221
1171549564171549565AG70GENICpossibly homozygous108378223
1171549976171549977AG51GENIChomozygous108378225
1171550183171550184GA33GENICpossibly homozygous108378227
1171550803171550804TC66GENIChomozygous108378229
1171552541171552542CT18GENICpossibly homozygous108378231
1171555206171555207AG46GENICheterozygous109523877
1171560252171560253AC59GENICpossibly homozygous108378235
1171560936171560937GC50GENICheterozygous108378238
1171563071171563072TC49GENIChomozygous108378240
1171562616171562617CT49GENIChomozygous108959601