chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140887210140887211TG37GENIChomozygous789361565
4140887405140887406GC28GENIChomozygous789361566
4140887526140887527AG19GENIChomozygous789361567
4140887695140887696GA26GENIChomozygous789361568
4140888161140888162GT19GENIChomozygous789361569
4140894149140894150GA22GENIChomozygous789361570
4140896988140896989GA32GENIChomozygous789361571
4140897414140897415CT18GENIChomozygous789361572
4140902715140902716TC16GENIChomozygous789361573
4140902957140902958AG22GENIChomozygous789361574
4140903807140903808CT21GENIChomozygous789361575
4140906350140906351AG31GENIChomozygous789361576
4140906395140906396AG40GENIChomozygous789361577
4140907673140907674TC23GENICheterozygous789361578
4140908274140908275TG18GENIChomozygous789361579
4140908798140908799AG40GENIChomozygous789361580
4140908994140908995GC15GENIChomozygous789361581
4140909196140909197CT31GENIChomozygous789361582
4140909244140909245GT25GENIChomozygous789361583
4140909248140909249TA25GENIChomozygous789361584
4140916630140916631TG20GENIChomozygous789361585
4140916631140916632CA19GENIChomozygous789361586
4140916796140916797CG22GENIChomozygous789361587