chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107386792773867928CT34GENIChomozygous116635605
107386809273868093AG44GENIChomozygous116635607
107386889273868893TC53GENICpossibly homozygous116635609
107386922073869221CT43GENIChomozygous116635611
107386999273869993AG11GENIChomozygous116635613
107387005473870055AG19GENIChomozygous116635615
107387063373870634GA31GENIChomozygous116635617
107387091373870914AG5GENIChomozygous118001263
107387095073870951CT8GENICpossibly homozygous118001264
107387096173870962TG9GENIChomozygous118001265
107387096573870966GA9GENICheterozygous118001266
107387097473870975TG10GENIChomozygous118001267
107387129373871294AG51GENIChomozygous117064234
107387164673871647TA47GENIChomozygous116635619
107387227273872273TC57GENIChomozygous116635621
107387269573872696CT51GENIChomozygous118001268
107387479573874796GT26GENICpossibly homozygous118001269
107387479973874800GT25GENICpossibly homozygous116800120
107387480373874804GT25GENICpossibly homozygous116800122
107387480773874808GT25GENICpossibly homozygous116893536
107387887573878876GA30GENIChomozygous117064238
107388149673881497TC52GENIChomozygous116635631
107387515073875151TC53GENIChomozygous116635623
107387620673876207CG59GENIChomozygous116635625
107387727173877272AG41GENIChomozygous116635627
107387739073877391GA27GENIChomozygous116635629
107388544973885450GA54GENIChomozygous116635633