chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4153753142153753143TG27GENIChomozygous112890356
4153753153153753154TA27GENIChomozygous112890357
4153753934153753935AG19GENIChomozygous112890358
4153755071153755072TC35GENIChomozygous112890359
4153755224153755225CT26GENIChomozygous112890360
4153755342153755343GT24GENICpossibly homozygous112890361