chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7122150594122150595GC16GENIChomozygous634728854
7122150826122150827CCCA6GENICheterozygous747617006
7122155180122155181AAG10GENIChomozygous747617009
7122155864122155865TC51GENICpossibly homozygous634728855
7122156385122156386TTTGTTTCTTGGGGTTGGGGATTTAGCTCA16GENICheterozygous747617010
7122156596122156597AG16GENIChomozygous634728856
7122156620122156621T-18GENICpossibly homozygous747617011
7122173531122173543GTTTGTTTGTTT------------12GENIChomozygous747617016