chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18400026984000270GC34GENIChomozygous120514119
18400088784000888GT31GENIChomozygous108879826
18400088884000889AT32GENIChomozygous108879827
18400090184000902AG30GENIChomozygous120667205
18400108984001090GC35GENIChomozygous108879828
18400121084001211CT26GENIChomozygous108879829
18400138984001390AC18GENIChomozygous108879830
18400161884001619GA23GENIChomozygous108879831
18400227384002274GT14GENIChomozygous108879832
18400247284002473CT33GENIChomozygous108879833
18400283084002831TC25GENIChomozygous108879834
18400284084002841GT26GENIChomozygous108879835
18400327084003271TC28GENIChomozygous108879836
18400353984003540TC28GENIChomozygous108879837
18400361484003615AG29GENIChomozygous108879838
18400378784003788TC28GENIChomozygous108879839
18400400084004001CT28GENIChomozygous108879840
18400475884004759AC29GENIChomozygous108879841
18400527084005271TC20GENIChomozygous108879842
18400578284005783CG37GENICpossibly homozygous108879843
18400767184007672CT28GENIChomozygous108879844
18400814584008146AT12GENIChomozygous108879845
18400841084008411CA22GENIChomozygous108879846