chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141882273141882274CT40GENICheterozygous54159946
7141882400141882401GGA24GENICheterozygous54159947
7141883104141883105CCA32GENICheterozygous54159949
7141883133141883134CT27GENICheterozygous54159950
7141884986141884987TC36GENICheterozygous54159957
7141885539141885540TC42GENICheterozygous54159958
7141885551141885552AG47GENICheterozygous54159959
7141890860141890861TC20GENICheterozygous54159969
7141894098141894099GA231GENICheterozygous54159975
7141894119141894120TC231GENICheterozygous54159976
7141894200141894201GA250GENICheterozygous54159980
7141894211141894212TC250GENICheterozygous54159981
7141894369141894370AG204GENICheterozygous54159984
7141894386141894387GA160GENICheterozygous54159985
7141894388141894389AACTTC150GENICheterozygous54159986
7141895476141895477CG8GENICheterozygous54160017
7141899795141899796AG30GENICheterozygous54160024
7141911811141911812TA30GENICheterozygous54160056
7141915652141915653T-27GENICheterozygous54160058
7141917652141917653AG12GENICheterozygous54160059
7141918197141918198AG74GENICheterozygous54160061
7141918244141918245AG54GENICheterozygous54160062
7141920111141920112GGCAGA10INTERGENICheterozygous54160063