chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2115336846115336846G5GENIChomozygous127668036
2115337443115337444AG59GENIChomozygous109987359
2115337455115337456GC59GENIChomozygous109987361
2115341312115341313GA69GENIChomozygous109987368
2115337657115337658AC50GENICpossibly homozygous109987363
2115337921115337922GC51GENIChomozygous109987364
2115340324115340325GA64GENIChomozygous109987366
2115341587115341588CT71GENIChomozygous109987370
2115341633115341634GA69GENIChomozygous109987372
2115342624115342625CG50GENIChomozygous109987374
2115343356115343357AG30GENIChomozygous109987376
2115343371115343372AG31GENIChomozygous109987377
2115343716115343717TC65GENIChomozygous109987379
2115344071115344071CCTG65GENIChomozygous127668037
2115344789115344790GA53GENIChomozygous109987381
2115345434115345435T63GENIChomozygous127668038
2115345445115345446AT62GENIChomozygous109987383
2115345463115345464TA58GENIChomozygous109987385
2115345473115345474AG62GENIChomozygous109987387
2115346038115346039AG69GENIChomozygous109987388
2115346325115346326AG62GENIChomozygous109987390
2115346372115346372A61GENIChomozygous127668039
2115347724115347725AG59GENIChomozygous109987392
2115347892115347893TA65GENICheterozygous109987394
2115348436115348448CCTGCTGCTCCC4GENIChomozygous127668040
2115348917115348918GT57GENIChomozygous109987396
2115349739115349740TG62GENIChomozygous109987397
2115351727115351735CAATGTAC57GENIChomozygous127668041
2115352644115352645AG63GENIChomozygous109987399