chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5141281556141281557GA27GENIChomozygous137640456
5141282483141282483AC11GENIChomozygous137346337
5141282576141282576CA12GENICpossibly homozygous137346338
5141284160141284161TC14GENIChomozygous137640457
5141285445141285446AC15GENIChomozygous137640458
5141286597141286597C21GENIChomozygous137346339
5141288167141288168TC15GENIChomozygous137640459
5141288501141288502TC20GENIChomozygous137640460
5141289362141289363GA34GENIChomozygous137640461
5141290389141290389TCTTCCTCTTCCCCCCTCCCCG9GENIChomozygous137346340
5141293653141293654TC18GENIChomozygous137640468
5141293950141293951GA23GENIChomozygous137640469
5141294972141294973TG22GENIChomozygous137640470
5141295213141295214AG11GENIChomozygous137640471
5141296269141296270CT13GENIChomozygous137640472
5141296466141296467TC21GENIChomozygous137640473
5141297070141297071TC9GENIChomozygous137640474
5141297474141297475TC20GENIChomozygous137640475
5141298490141298491CT17GENIChomozygous137640476
5141298792141298792AT26GENIChomozygous137346342
5141299063141299067ACAA15GENIChomozygous137346343
5141299618141299619AG22GENIChomozygous137640477
5141300434141300435TC22GENIChomozygous137640478
5141301002141301002TCT16GENIChomozygous137346344
5141301382141301383GA15GENIChomozygous137640479
5141302974141302975A14GENIChomozygous137346345
5141304130141304131GA19GENIChomozygous137640480
5141304503141304504AT12GENIChomozygous137640481
5141305076141305077GA12GENIChomozygous137640482
5141305766141305767GA13GENIChomozygous137640483
5141306875141306876TC21GENIChomozygous137640484
5141307320141307321T16GENIChomozygous137346346
5141308417141308418AG27GENIChomozygous137640485
5141308529141308529CTTT18GENIChomozygous137346347
5141309587141309588CT13GENIChomozygous137640486
5141283744141283745C8GENIChomozygous403160843
5141283744141283745CT8GENICheterozygous403160844