chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9100849165100849166CT29GENIChomozygous120283413
9100850066100850067GA26GENIChomozygous120283414
9100850507100850508AG21GENIChomozygous117620189
9100851661100851662CT9GENIChomozygous120283416
9100853680100853681GA20GENIChomozygous120283417
9100854250100854251AT38GENIChomozygous120364144
9100854684100854685GA31GENIChomozygous117764437
9100857003100857004GA32GENIChomozygous117620200
9100858535100858536TA16GENIChomozygous120283418
9100860210100860211GC28GENIChomozygous120283419
9100861713100861714GA8GENIChomozygous120283420
9100863695100863696CT33GENIChomozygous120283421
9100864124100864125TC36GENIChomozygous117620206
9100865863100865864AG52GENIChomozygous117620208
9100875115100875116CT23GENIChomozygous117620224
9100875529100875530AC26GENIChomozygous117620226
9100876814100876815AC10GENIChomozygous120283422
9100876818100876819AC14GENIChomozygous117620228
9100878674100878675CT25GENIChomozygous117620230
9100879200100879201TA16GENIChomozygous117620232
9100881759100881760TC18GENIChomozygous117620234
9100884477100884478GA39GENIChomozygous117620236
9100885091100885092TC28GENIChomozygous117620238
9100885551100885552GT28GENIChomozygous117400502
9100885856100885857CT35GENIChomozygous120283423
9100886289100886290AG26GENIChomozygous117620240
9100886741100886742AG20GENIChomozygous117794998
9100887509100887510AG18GENIChomozygous117620242