chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109410549494105495CCAA3GENICheterozygous51548070
109410549594105497AA--3GENICheterozygous51548071
109410549694105497A-3GENICheterozygous51548072
109410619794106199GA--38GENIChomozygous51548073
109410630594106306TC49GENIChomozygous51548074
109410914894109149CT61GENICpossibly homozygous51548075
109410942594109426TG28GENIChomozygous51548076
109411086794110868AT46GENIChomozygous51548077
109411097894110979CG55GENIChomozygous51548078
109411128894111289TG38GENIChomozygous51548079
109411156194111562GGA68GENIChomozygous51548080
109411175994111760AG47GENIChomozygous51548081
109411215294112153AG37GENIChomozygous51548082
109411307794113078AC36GENICheterozygous51548083
109411318094113181TC52GENIChomozygous51548084
109411352794113528CT53GENIChomozygous51548085
109411372694113727AT45GENIChomozygous51548086
109411449894114499GA64GENIChomozygous51548087
109411517094115172AA--22GENICheterozygous51548088
109411517194115172A-22GENICheterozygous51548089
109411572694115744TGTGTGTGTGTGTGTGTG------------------18GENIChomozygous51548090
109411679694116797GA64GENIChomozygous51548091
109411705594117056GC44GENIChomozygous51548092
109411721894117219GA27GENIChomozygous51548093
109412033594120336A-29GENICpossibly homozygous51548094
109412113994121140T-15GENICheterozygous51548095
109412273394122737AAAT----9GENIChomozygous51548096
109412462294124623A-25GENIChomozygous51548097
109412561394125614T-6GENIChomozygous51548098
109412594794125948GA45GENIChomozygous51548099
109413035594130356GA36GENIChomozygous51548100
109413226994132270CCT19GENICheterozygous51548101
109413226994132270CCTT19GENICheterozygous51548102