chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
22514436625144367CT16GENIChomozygous110491136
22514656625146567CG24GENIChomozygous110491138
22514666625146667TC19GENIChomozygous110491140
22514673325146734CG17GENIChomozygous110491142
22514675425146755TA15GENIChomozygous110491144
22514678025146781AT17GENIChomozygous110491146
22514685525146856AG7GENIChomozygous110491148
22514685725146858GT6GENIChomozygous110491150
22514717125147172AG22GENIChomozygous110491152
22514728525147286AC10GENIChomozygous110491154
22514730125147302CT12GENIChomozygous110491156
22514743125147432AG16GENIChomozygous110491158
22514743225147433TC16GENIChomozygous110491160
22514955525149556TC11GENIChomozygous109649525
22515047825150479GA16GENIChomozygous109649529
22515054025150541CT11GENIChomozygous109649531
22515089225150893CT4GENICheterozygous125638041
22515310125153102AG24GENIChomozygous109649533
22514747825147479TA7GENIChomozygous120141086