chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7544796875447969AG36GENICheterozygous783308121
X7544825075448251AT62GENICheterozygous783308122
X7544830075448301GA9GENIChomozygous783308123
X7544832575448326AG7GENIChomozygous783308124
X7544832675448327AC8GENIChomozygous783308125
X7544838475448385GA21GENIChomozygous783308126
X7544841475448415GA31GENICpossibly homozygous783308127
X7546122975461230TG16GENIChomozygous783308128
X7546830375468304CG34GENIChomozygous783308129
X7546834775468348CG45GENIChomozygous783308130
X7546878475468785TA4GENIChomozygous783308131
X7548242275482423TC58GENICheterozygous783308132
X7548243075482431TC58GENICheterozygous783308133
X7548274675482747TG111GENICheterozygous783308134
X7548275175482752CT117GENICheterozygous783308135
X7549355675493557CT40GENICpossibly homozygous783308136
X7549952575499526GA112GENICheterozygous783308137
X7549958075499581GC98GENICheterozygous783308138
X7549958375499584GA93GENICheterozygous783308139
X7549959275499593GA102GENICheterozygous783308140
X7549961975499620CG83GENICheterozygous783308141
X7549963875499639TC73GENICheterozygous783308142
X7551191075511911GT68GENIChomozygous783308143
X7551199575511996AT50GENIChomozygous783308144
X7551212475512125GT52GENICpossibly homozygous783308145
X7551217175512172TG58GENICpossibly homozygous783308146
X7551242875512429GT31GENIChomozygous783308147
X7551247375512474CT10GENIChomozygous783308148
X7554109775541098CA74GENICheterozygous783308149
X7555106175551062CT225GENICheterozygous783308150