chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51467969414679695AG61GENIChomozygous137384694
51467993514679936CT58GENIChomozygous137384695
51468469014684691TC48GENIChomozygous137384696
51468503914685040TC46GENIChomozygous137384697
51468579014685791GA42GENIChomozygous137384698
51469079214690793AC63GENIChomozygous137384699
51469178414691785AG53GENIChomozygous137384700
51469440414694405CT50GENIChomozygous137384701
51469688614696887CG39GENIChomozygous137384702
51470335714703358AC47GENIChomozygous137384703
51470610014706101AG29GENICheterozygous403592752
51469933314699334AT28GENICpossibly homozygous154264964
51470609814706099AG29GENICheterozygous154264966
51469933314699334A28GENICheterozygous403891982
51470609814706099A29GENICpossibly homozygous403592750
51470610014706101A29GENICpossibly homozygous403592751
51470668914706690TA39GENIChomozygous137384704
51470753714707538TC59GENIChomozygous137384705
51470610614706107AG31GENICheterozygous146774420
51469216814692168ACAC50GENIChomozygous137291855
51470610214706103A29GENICpossibly homozygous403891983
51470610214706103AG29GENICheterozygous403891984
51470610414706105AG29GENICpossibly homozygous154264967
51470610414706105A29GENICheterozygous403993640