chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
114330980243309803TC38GENIChomozygous118194269
114330982243309823GA42GENICpossibly homozygous118194270
114331003343310034TC54GENICheterozygous118194271
114331003743310038GA55GENICheterozygous118194272
114331020743310208CT84GENICheterozygous118194273
114331020943310210GA82GENICheterozygous118194274
114331021443310215GT82GENICheterozygous118194275
114331028143310282GT106GENICheterozygous115962957
114331032243310323CT102GENICheterozygous116243922
114331032843310329CT94GENICheterozygous116243924
114331033243310333GC92GENICheterozygous116243926
114331033543310336TA93GENICheterozygous116243928
114331034043310341CT92GENICheterozygous116243930
114331036243310363TC95GENICheterozygous116243931
114331037343310374CT89GENICheterozygous115962958
114331037743310378CG89GENICheterozygous115962959
114331038243310383TC92GENICheterozygous115962960
114331038843310389GT88GENICheterozygous115962961
114331039543310396AT86GENICheterozygous115962962
114331039743310398TA84GENICheterozygous115962963
114331040443310405GA79GENICheterozygous115962964
114331046343310464CG70GENICheterozygous115962965
114331046643310467GA71GENICheterozygous115962966
114331046943310470TC69GENICheterozygous115962967
114331047243310473TC70GENICheterozygous115962968
114331053543310536CT69GENICheterozygous116243933
114331054443310545CT71GENICheterozygous116243935
114331060143310602TA81GENICheterozygous115962969
114331062543310626CA82GENICheterozygous116243937