chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141882273141882274CT45GENICheterozygous54159946
7141882400141882401GGA28GENICheterozygous54159947
7141883104141883105CCA17GENICheterozygous54159949
7141883133141883134CT17GENICheterozygous54159950
7141884986141884987TC40GENICheterozygous54159957
7141885539141885540TC33GENICheterozygous54159958
7141885551141885552AG35GENICheterozygous54159959
7141890860141890861TC29GENICheterozygous54159969
7141894075141894076TC161GENICheterozygous54529730
7141894098141894099GA168GENICheterozygous54159975
7141894119141894120TC179GENICheterozygous54159976
7141894137141894138T-179GENICheterozygous54159977
7141894183141894184TC178GENICheterozygous54159979
7141894200141894201GA182GENICheterozygous54159980
7141894211141894212TC182GENICheterozygous54159981
7141894275141894276T-155GENICheterozygous54159982
7141894347141894348GA110GENICheterozygous54159983
7141894369141894370AG87GENICheterozygous54159984
7141894386141894387GA65GENICheterozygous54159985
7141894388141894389AACTTC63GENICheterozygous54159986
7141895476141895477CG13GENICheterozygous54160017
7141899795141899796AG18GENICheterozygous54160024
7141911811141911812TA28GENICheterozygous54160056
7141915652141915653T-15GENICheterozygous54160058
7141918197141918198AG32GENICheterozygous54160061
7141918244141918245AG21GENICheterozygous54160062
7141920111141920112GGCAGA15INTERGENICheterozygous54160063