chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
132715357827153578TAT20GENIChomozygous129036294
132715412527154126TC13GENIChomozygous118438019
132715536527155366CT20GENIChomozygous114608679
132715540127155402GA22GENIChomozygous114608680
132715610127156102GA15GENIChomozygous114303488
132715448427154485GT13GENIChomozygous114303485
132715520827155209CT14GENIChomozygous114303486
132715609427156095GA15GENIChomozygous114303487
132715613127156132A19GENIChomozygous129036295
132715614327156144AC19GENIChomozygous114303489
132715617327156174TC22GENIChomozygous114303490
132715630327156304TC20GENIChomozygous114303491
132715634627156347TC18GENIChomozygous114303492
132715702227157024AC10GENIChomozygous129036296
132715710027157101GC11GENIChomozygous114303493
132715713227157133CT10GENIChomozygous114303494
132715717827157179CT12GENIChomozygous114303495
132715722427157225TC13GENIChomozygous114303496
132715732827157329AG18GENIChomozygous114303497
132715736127157362CT18GENIChomozygous114303498
132715752927157529G16GENIChomozygous129036297
132715753027157530CAG16GENIChomozygous129036298
132715803127158032TA12GENIChomozygous114303499
132715833827158339TC10GENIChomozygous114303500
132715905327159054GA13GENIChomozygous114303501
132715917127159172AC19GENIChomozygous114303502