chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101354802913548030CT11GENICheterozygous51621451
101354804713548048GA12GENICheterozygous51621452
101354806413548065AG13GENICheterozygous51621453
101355309713553098GA26GENICheterozygous51621519
101355322913553230CT21GENICheterozygous51621520
101355323513553236TC20GENICheterozygous51621521
101355342213553423GA11GENICheterozygous51621522
101355452713554528CT37GENICheterozygous51621535
101355462513554626GT58GENICheterozygous51621536
101355465213554653GA55GENICheterozygous51621537
101355467413554675AG58GENICheterozygous51621538
101355478813554789CT34GENICheterozygous51621539
101355494513554946TA18GENICheterozygous51621540
101355550613555507CT26GENICheterozygous51621547
101355556213555563GT35GENICheterozygous51621548
101357243013572431GA24GENICheterozygous51621649
101357504913575050TC14GENICheterozygous51621652
101358628913586290GA19GENICheterozygous51621679
101358829713588298CT17GENICheterozygous51621685
101358849313588494GA18GENICheterozygous51621686
101358875013588751AG21GENICheterozygous51621687
101359277313592774AG24GENICheterozygous51621701
101359668613596687TC5GENICheterozygous51621710