chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
79183323691833237CT48GENICpossibly homozygous116051311
79183472091834721CT38GENIChomozygous116051313
79184525391845254GT51GENIChomozygous116051317
79185356491853565CT56GENIChomozygous115761191
79185679391856794CT37GENIChomozygous116051319
79185702991857030TC56GENIChomozygous115761195
79185896891858969GA29GENICpossibly homozygous116051321
79186856191868562GA44GENIChomozygous116051325
79186317191863172AG35GENICheterozygous116392212