chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123856772938567730AC16GENIChomozygous115323249
123856784238567843TC24GENIChomozygous115382663
123856790138567902AG21GENIChomozygous115323251
123856923238569233CT28GENIChomozygous115609673
123857013538570136CT18GENIChomozygous115609675
123857151838571519CG24GENIChomozygous115323263
123857166038571661CA18GENIChomozygous115382669
123857216938572170CT7GENIChomozygous115382671
123858373238583733TC16GENIChomozygous115323279
123860489338604894CA13GENIChomozygous115323313
123860489438604895TC13GENIChomozygous115323315
123860520838605209AC18GENIChomozygous115323317
123861132438611325AG19GENIChomozygous115609677
123861514538615146TC39GENIChomozygous115323321
123861514838615149GT41GENIChomozygous115323323
123861517238615173TC35GENIChomozygous115323325
123861518338615184AT33GENIChomozygous115323327
123861520738615208GA29GENIChomozygous115323329
123861521138615212GT30GENIChomozygous115323331
123861804538618046GA35GENIChomozygous115609679
123861957338619574TC12GENIChomozygous115323341
123862115038621151GA31GENIChomozygous115323343
123862776038627761AG14GENICheterozygous115609681
123862776238627763AG11GENICheterozygous115609683
123863504338635044AT29GENIChomozygous115609685