chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------21GENIChomozygous747672791
85378107053781071CT36GENIChomozygous634812952
85378121053781211AG28GENIChomozygous634812953
85378128753781288GGA20GENICheterozygous747672793
85378128753781288GGAA20GENICheterozygous747672794
85378128753781288GGAAA20GENICheterozygous747672795
85378133353781334AG25GENIChomozygous634812954
85378146653781467AG35GENIChomozygous634812955
85378180553781806AG24GENIChomozygous634812956
85378193153781932TTTA11GENICheterozygous747672796
85378193153781932TTTTA11GENICheterozygous747672797
85378200853782013GTTTG-----12GENIChomozygous747672799
85378241353782414CT37GENIChomozygous634812957
85378260753782608TC25GENIChomozygous634812958
85378268153782682GGGTGT1GENIChomozygous747672800
85378277053782771GA19GENIChomozygous634812959
85378331953783320AG15GENIChomozygous634812960
85378340253783403T-11GENIChomozygous747672801
85378373853783739GT35GENIChomozygous634812961
85378379353783794TC43GENIChomozygous634812962
85378391753783918T-18GENIChomozygous747672802
85378391953783926TGCGTGT-------19GENICpossibly homozygous747672803
85378404853784049TC34GENIChomozygous634812963
85378550553785506T-4GENIChomozygous747672804
85378552153785522CCTTTT9GENIChomozygous747672806