chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101381609713816098CCACTCCGAAGAGGCAGCTCCCCT34GENIChomozygous759276915
101381615313816154AG28GENIChomozygous653712686
101381689013816891GGGTGTGTGT5GENICheterozygous759276917
101381704213817043AG26GENICpossibly homozygous653712687
101381816313818164GGC9GENIChomozygous759276919
101381836213818363GA33GENICpossibly homozygous653712688
101381886213818863CCA20GENICpossibly homozygous759276920
101381920013819201A-38GENIChomozygous759276921