chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115512383115512384CT26GENICheterozygous924547082
8115513030115513031CT11GENICheterozygous924547083
8115516330115516331CCG83GENICheterozygous924587674
8115518076115518077AG28GENICheterozygous924547084
8115519250115519251GA13GENICheterozygous924547085
8115523834115523835AG33GENICheterozygous924547086
8115527949115527950AC11GENICheterozygous924547087
8115527950115527951GA11GENICheterozygous924547088
8115541589115541590AAG25GENICheterozygous924587675
8115555931115555932CT48GENICheterozygous924547089
8115557483115557484AG10GENICheterozygous924547090
8115559439115559440AG23GENICheterozygous924547091
8115570286115570287TTC47GENICheterozygous924587676
8115575447115575448TC39GENICheterozygous924547092
8115579013115579014TTGG18GENICheterozygous924587677
8115580541115580542GA24GENICheterozygous924547093
8115583695115583696CT22GENICheterozygous924547094
8115592854115592855AG23GENICheterozygous924547095
8115623017115623018CT24GENICheterozygous924547096
8115632953115632954CT38GENICheterozygous924547097
8115635013115635014GA31GENICheterozygous924547098
8115638507115638508TA17GENICheterozygous924547099
8115639625115639626TA13GENICheterozygous924547100
8115641601115641602AAC39GENICheterozygous924587678