chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85191367951913680TC6GENIChomozygous52974749
85191441751914418GA26GENICpossibly homozygous52974750
85191564951915650TC20GENIChomozygous52974752
85191707351917074GA23GENICpossibly homozygous52974753
85191768251917683GA4GENIChomozygous52974755
85191777151917772TTGCGCGCGC1GENIChomozygous52974756
85191779051917792GC--1GENIChomozygous53507727
85191779951917800CT3GENICheterozygous52974758
85191825251918253TC6GENICheterozygous52974759
85191895651918957TC23GENICpossibly homozygous52974760
85192060151920602TC21GENICpossibly homozygous52974763
85192113851921139CT9GENIChomozygous52974766
85192211751922118GA11GENIChomozygous52974767
85192306651923068AT--7GENIChomozygous52974768
85192383551923836TG2GENICheterozygous52974771
85192460951924610CA21GENICpossibly homozygous52974772
85192506751925068GA13GENICpossibly homozygous52974773
85192569351925694TC10GENICheterozygous52974774
85192569451925695AT10GENICheterozygous52974775
85192648951926490TC20GENIChomozygous52974777
85192820351928204C-2GENICheterozygous53386814
85194238651942387GA24GENIChomozygous52974778
85194613251946133AAATTT2GENICheterozygous52974779
85194662251946623T-5GENICheterozygous53550545