chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161892529918925300AC52GENIChomozygous139889411
161892579318925794AG39GENIChomozygous144164224
161892582018925821AG26GENIChomozygous144164225
161892583918925839C29GENIChomozygous144156744
161892620018926201TA53GENICpossibly homozygous142533686
161892625618926257CA60GENICpossibly homozygous144164226
161892714418927145AG47GENIChomozygous139889413
161892730518927306TC56GENIChomozygous144164227
161892836818928369GA54GENIChomozygous144164228
161892842118928422GA54GENIChomozygous144164229
161892851218928513TC55GENIChomozygous144164230
161892879118928792CT49GENIChomozygous144164231
161892905618929057C33GENICpossibly homozygous139824734
161893066818930669GA44GENIChomozygous144164232
161893085118930852AG34GENIChomozygous144164233
161893115318931153AT43GENIChomozygous144156745
161893117618931177AG41GENIChomozygous144164234
161893136218931363GT33GENICpossibly homozygous144164235
161893220918932210CT67GENIChomozygous148784362
161893266618932667TC58GENIChomozygous139889416
161893520518935206GA42GENIChomozygous148784363
161893272818932728ATAAATAG50GENIChomozygous148782787
161893249418932502TTCATTCA51GENIChomozygous148782786