chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101381609713816098CCACTCCGAAGAGGCAGCTCCCCT20GENIChomozygous746021079
101381615313816154AG17GENIChomozygous632175766
101381689013816891GGGTGTGT8GENICheterozygous746021080
101381689013816891GGGTGTGTGT8GENICheterozygous746021081
101381704213817043AG28GENIChomozygous632175767
101381816313818164GGC14GENICpossibly homozygous746021083
101381836213818363GA31GENIChomozygous632175768
101381886213818863CCA30GENIChomozygous746021084
101381920013819201A-24GENIChomozygous746021085