chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141313531013135311AG63GENICheterozygous48945191
141313537913135380TTTGTGTGTGTG40GENICheterozygous49467295
141313552213135523TA20GENICheterozygous49276899
141314136913141370CG27GENICheterozygous49276900
141319400013194001AG23GENICheterozygous48525492
141319984313199844GA26GENICheterozygous48525502
141319991213199913AC22GENICheterozygous49276914
141319995713199966CATGCTTCC---------12GENICheterozygous48525504
141319996713199968TC10GENICheterozygous49276915
141320046213200463CT22GENICheterozygous48525516
141320054113200542T-23GENICheterozygous48525518
141320641813206419AT39GENICheterozygous49276932
141321616913216170TA30GENICheterozygous49276958
141321631713216318TC24GENICheterozygous49276959
141321663413216635GC20GENICheterozygous49276960
141321666213216663CT21GENICheterozygous49276961
141321928513219286AG5GENICheterozygous48525559
141322773913227740AG18GENICheterozygous49193646
141323146713231468AATT17GENICheterozygous48525609
141323492613234927GA24GENICheterozygous48525709
141323505313235054AG16GENICheterozygous48525712
141326583313265834CT35GENICheterozygous49276996
141327168513271686GA28GENICheterozygous49193732
141327169913271700AT27GENICheterozygous48945699
141327276713272768GT26GENICheterozygous48525975