chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2275576484275576485TTG9GENICpossibly homozygous59587112
2275578217275578218TTA8GENIChomozygous59587117
2275578240275578241C-5GENIChomozygous59587118
2275578246275578247TTA5GENICheterozygous59587119
2275580692275580693GGT16GENICpossibly homozygous59587126
2275580752275580753TC5GENIChomozygous59587129
2275580766275580767AC4GENIChomozygous59587130
2275581489275581490CCA23GENIChomozygous59587134
2275585739275585740GGTAAATAAA3GENIChomozygous59985699
2275585932275585936ACAC----19GENICheterozygous60188134
2275585934275585936AC--19GENICheterozygous60188135
2275586094275586095CT23GENIChomozygous59587149
2275586587275586588TG23GENIChomozygous59587150
2275587083275587084TA20GENIChomozygous59587153
2275587156275587157TA15GENIChomozygous59587154
2275588280275588281TG17GENIChomozygous59587156
2275588402275588403TA20GENIChomozygous59985706
2275588586275588587CT16GENIChomozygous60265583
2275590175275590176CT12GENIChomozygous60265584
2275590639275590640GT32GENIChomozygous60265585
2275591165275591166AG20GENIChomozygous59587158
2275591994275591995TC9GENIChomozygous59587159
2275592881275592882AC14GENIChomozygous60188142
2275593023275593024CT10GENIChomozygous60265586
2275593059275593060TA9GENIChomozygous60188143
2275593535275593536GT18GENIChomozygous60265587