chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101410575314105754CT42GENIChomozygous51622750
101410600514106006CA17GENIChomozygous51622751
101410891014108911CT38GENIChomozygous51622752
101410894714108948CCA27GENICpossibly homozygous51622754
101410975114109752A-16GENIChomozygous51622756
101410989914109900GT14GENIChomozygous51622757
101411036114110363AT--6GENIChomozygous52481305
101411036714110373ACACAT------10GENICheterozygous52481307
101411043114110432A-28GENICheterozygous52481309
101411141914111420CCA14GENICheterozygous52431573
101411144414111446TT--23GENICheterozygous52481311