chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4153751774153751775CT24GENICpossibly homozygous112890354
4153751818153751819TC32GENIChomozygous112890355
4153753142153753143TG27GENIChomozygous112890356
4153753153153753154TA30GENIChomozygous112890357
4153753934153753935AG31GENIChomozygous112890358
4153755071153755072TC33GENIChomozygous112890359
4153755224153755225CT36GENIChomozygous112890360
4153755342153755343GT49GENICpossibly homozygous112890361