chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55655520956555210CA87GENICpossibly homozygous780164949
55655563956555640GC34GENIChomozygous780164950
55655610056556101TG71GENIChomozygous780164951
55655687156556872AC60GENIChomozygous780164952
55655739456557395TC59GENIChomozygous780164953
55655883856558839AT77GENIChomozygous780164954
55655903656559037AG58GENIChomozygous780164955
55655949856559499AT64GENIChomozygous780164956
55655986656559867TC79GENICpossibly homozygous780164957
55656006956560070GA42GENICheterozygous780164958
55656016356560164CT30GENICheterozygous780164959
55656075656560757CT82GENICheterozygous780164960
55656078356560784AG30GENICpossibly homozygous780164961
55656079556560796CT33GENICheterozygous780164962
55656080256560803CT37GENICheterozygous780164963
55656081356560814AG40GENICheterozygous780164964
55656093156560932CT71GENIChomozygous780164965
55656100456561005AG58GENIChomozygous780164966
55656114056561141GT40GENIChomozygous780164967
55656208056562081CT62GENIChomozygous780164968
55656254656562547TC68GENIChomozygous780164969
55656318756563188TC42GENIChomozygous780164970
55656330756563308TA49GENIChomozygous780164971
55656435356564354CA51GENIChomozygous780164972
55656514356565144TG43GENIChomozygous780164973
55656521156565212AG43GENIChomozygous780164974
55656583756565838CT65GENIChomozygous780164975
55656616956566170TC46GENIChomozygous780164976
55656621356566214GA33GENIChomozygous780164977