chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37673646476736464TATG34GENIChomozygous145393783
37674866976748670T45GENIChomozygous145393784
37675103976751040GC44GENIChomozygous136754910
37675160376751604GA38GENIChomozygous136754912
37675219176752192T25GENIChomozygous136574118
37675232576752326TG22GENICpossibly homozygous145415300
37675230376752304T17GENICheterozygous404411907
37675230376752304TA17GENIChomozygous404411908
37674480476744805GA28GENIChomozygous145415297
37674867076748671TA46GENIChomozygous145415298
37674991676749917CT56GENIChomozygous145415299
37675275476752755AC44GENIChomozygous136754913
37675315276753153A34GENICheterozygous403765698
37675315276753153AT34GENICheterozygous403765699
37675315376753154A34GENICheterozygous403811413
37675315376753154AT34GENICheterozygous403811414
37675324876753249TC45GENIChomozygous136754914
37675368076753681CT37GENIChomozygous145415301
37675394576753946TC41GENIChomozygous145415302
37675406876754069AC42GENIChomozygous145415303
37675458176754582TC40GENIChomozygous136754916
37675496776754968AG30GENIChomozygous145415304
37675534976755350CG33GENIChomozygous145415305
37675547476755475AG21GENIChomozygous145415306
37675554476755545GT38GENIChomozygous145415307
37675581776755818GA43GENIChomozygous136754918
37675638476756385AT43GENIChomozygous145415308
37675740876757409GA43GENIChomozygous145415309
37675747676757478AG45GENIChomozygous145393785
37675748276757483TG44GENIChomozygous136754921
37675892276758924TG21GENICpossibly homozygous145393786
37675893976758940TG21GENICpossibly homozygous145415310
37675895776758960TTC27GENICpossibly homozygous136574123
37675904676759047GA29GENIChomozygous136754922
37676010676760107CT41GENIChomozygous145415311
37676155076761551GA41GENIChomozygous136754924
37676158076761581CT45GENIChomozygous136754925
37676170476761705CT44GENIChomozygous136754926
37676229676762297CT47GENIChomozygous136754929
37676288876762889TC36GENIChomozygous136754930