chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7141856671418566A11GENICheterozygous130719995
X7141856771418568CA12GENICheterozygous108391253
X7143550871435509GC17GENICheterozygous129817471
X7143552571435532GAGTCTG19GENICheterozygous129754037
X7143549471435496AG16GENICheterozygous129754034
X7143549771435501AACC16GENICheterozygous129754035
X7143552071435523TCT17GENICheterozygous129754036
X7143553771435538CT18GENICheterozygous129817472
X7143555771435558GC18GENICheterozygous129817473
X7143556471435565CT18GENICheterozygous129817474
X7143556571435566GA17GENICheterozygous129817475
X7143558271435583CT21GENICheterozygous129817476
X7143558771435588GA21GENICheterozygous129817477
X7143584871435849AG37GENICheterozygous120095424
X7143585171435852CT39GENICheterozygous120095425
X7143581371435814CT35GENICheterozygous120634466
X7143592571435926CT42GENICheterozygous120634467
X7143592871435929TA42GENICheterozygous120634468
X7143585571435856CT42GENICheterozygous119924831
X7143591571435916GT44GENICheterozygous119924832
X7143651571436516TC34GENICheterozygous129817487
X7143654871436549CG30GENICheterozygous129817488
X7143656971436570A24GENICheterozygous129754038
X7143657871436579AT21GENICheterozygous129817489
X7143658671436587AG21GENICheterozygous129817490
X7143661271436613CT24GENICheterozygous129817491
X7144845771448457T22GENICheterozygous130803560
X7146033871460339GA4GENICheterozygous132256978
X7146314771463148T14GENICheterozygous129754041
X7146458971464589T23GENICheterozygous129754042
X7148383771483838AC15GENIChomozygous108273259
X7148386171483861ATATAAGAATATTATCTC14GENIChomozygous129754043
X7144437371444374AG12GENIChomozygous108526538
X7145233671452336AC13GENIChomozygous132248878
X7146032971460330T3GENICheterozygous132248879
X7145694871456948T17GENICheterozygous130611537