chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55693321356933214AT45GENIChomozygous137475893
55693365156933652GA59GENIChomozygous137475894
55693727256937273TA57GENIChomozygous137475895
55693755156937552TC52GENIChomozygous137475896
55693775556937755TTTGGGCCAAGAA48GENIChomozygous137309995
55693775756937758GC48GENIChomozygous137475897
55693775956937760C48GENIChomozygous137309996
55693841356938414AG49GENIChomozygous137475898
55693896356938964CT49GENIChomozygous137475899
55693920756939208GA57GENICpossibly homozygous137475900
55693930656939307TC64GENIChomozygous137475901
55693974156939742AG60GENIChomozygous137475902
55694072656940727AG49GENIChomozygous137475903
55693880956938810GA20GENICheterozygous154299393
55693880956938810G20GENICheterozygous403142227