chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135578915955789170CTGTCTCTCTC-----------4GENIChomozygous769596339
135578917355789176TTC---2GENIChomozygous769596340
135578922755789228TTC3GENIChomozygous769596341
135578923655789237GGTC3GENIChomozygous769596342
135578927055789271TTTCTCTCTCTGTCTTCTCTCTGTCTCTGTCTCTCTCTCTTTC2GENIChomozygous769596343
135578961755789618GGTC25GENIChomozygous769596345
135578972455789725TTC11GENICheterozygous769596346
135578973155789732CCTCT10GENICpossibly homozygous769596347
135579115155791152GT28GENIChomozygous672410701
135579166055791661CT35GENIChomozygous672410702
135579200955792010GGCA16GENICheterozygous769596348
135579200955792010GGCACA16GENICheterozygous769596349
135579200955792010GGCACACA16GENICheterozygous769596350
135579214955792150GA34GENIChomozygous672410703
135579303055793031AG21GENIChomozygous672410704
135579307355793074T-24GENIChomozygous769596351
135579405955794060AAG11GENIChomozygous769596352
135579417355794174CA13GENIChomozygous672410705
135579501655795017CT25GENICpossibly homozygous672410706
135579512755795128AG27GENIChomozygous672410707
135579548355795484TC18GENIChomozygous672410708
135579568655795687GGC19GENIChomozygous769596353
135579639955796400GA32GENICpossibly homozygous672410709
135579807855798079AACACCC1GENIChomozygous769596356
135579808655798087AG9GENICheterozygous672410710
135579909955799100AC37GENIChomozygous672410711
135579987755799878AG23GENIChomozygous672410712
135580011755800118AC25GENICpossibly homozygous672410713
135580029855800299CT30GENICpossibly homozygous672410714
135580038555800386GA29GENIChomozygous672410715
135580062355800624CG24GENIChomozygous672410716
135580131055801311GT23GENICpossibly homozygous672410717
135580164955801650AG21GENIChomozygous672410718