chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
114330980243309803TC12GENIChomozygous118194269
114330982243309823GA14GENICpossibly homozygous118194270
114331003343310034TC22GENICheterozygous118194271
114331003743310038GA23GENICheterozygous118194272
114331020743310208CT38GENICheterozygous118194273
114331020943310210GA38GENICheterozygous118194274
114331021443310215GT39GENICheterozygous118194275
114331028143310282GT53GENICheterozygous115962957
114331032243310323CT45GENICheterozygous116243922
114331032843310329CT47GENICheterozygous116243924
114331033243310333GC45GENICheterozygous116243926
114331033543310336TA45GENICheterozygous116243928
114331034043310341CT46GENICheterozygous116243930
114331036243310363TC48GENICheterozygous116243931
114331037343310374CT45GENICheterozygous115962958
114331037743310378CG44GENICheterozygous115962959
114331038243310383TC45GENICheterozygous115962960
114331038843310389GT47GENICheterozygous115962961
114331039543310396AT48GENICheterozygous115962962
114331039743310398TA49GENICheterozygous115962963
114331046643310467GA43GENICheterozygous115962966
114331040443310405GA54GENICheterozygous115962964
114331046343310464CG44GENICheterozygous115962965
114331046943310470TC41GENICheterozygous115962967
114331047243310473TC44GENICheterozygous115962968
114331053543310536CT49GENICheterozygous116243933
114331054443310545CT50GENICheterozygous116243935
114331060143310602TA54GENICheterozygous115962969
114331062543310626CA46GENICheterozygous116243937