chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71294979112949792AG21GENIChomozygous115570738
71295152212951523GA32GENIChomozygous116275102
71295389212953893CT17GENICheterozygous116275104
71295393412953935TC28GENIChomozygous115570747
71295396512953966CA34GENICheterozygous116275106
71295401912954020AG21GENICpossibly homozygous115570748
71295414512954146CT12GENICheterozygous115570749
71295414612954147CT12GENICheterozygous115570750
71295519712955198CT27GENIChomozygous116275108
71295534012955341CG30GENIChomozygous115570752
71296569212965693CT32GENIChomozygous115570762
71296748712967488CT29GENIChomozygous116275110
71296785112967852TC27GENIChomozygous115570765
71296790012967901AC35GENICpossibly homozygous115570766
71296944012969441AG16GENIChomozygous115570767
71297058712970588AG36GENIChomozygous115570770
71297107012971071TC58GENICheterozygous115570772
71297107112971072GA58GENICheterozygous115570773
71297107812971079CT61GENICheterozygous115570774
71297108112971082CG61GENICheterozygous115570775