chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51467969414679695AG58GENIChomozygous137384694
51467993514679936CT45GENIChomozygous137384695
51468469014684691TC44GENIChomozygous137384696
51468503914685040TC40GENIChomozygous137384697
51468579014685791GA44GENIChomozygous137384698
51469079214690793AC35GENIChomozygous137384699
51469178414691785AG51GENIChomozygous137384700
51469440414694405CT53GENIChomozygous137384701
51469688614696887CG29GENICpossibly homozygous137384702
51469933314699334AT26GENICheterozygous154264964
51470335714703358AC47GENIChomozygous137384703
51470609814706099AG19GENICheterozygous154264966
51470610014706101AG19GENICheterozygous403592752
51469933314699334A26GENICheterozygous403891982
51470609814706099A19GENICheterozygous403592750
51470610014706101A19GENICheterozygous403592751
51470610214706103A19GENICheterozygous403891983
51470610214706103AG19GENICheterozygous403891984
51470610414706105AG19GENICheterozygous154264967
51470610414706105A19GENICheterozygous403993640
51470668914706690TA51GENIChomozygous137384704
51470753714707538TC44GENIChomozygous137384705
51470610614706107AG17GENICpossibly homozygous146774420
51469216814692168ACAC47GENIChomozygous137291855