chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
203533693635336937CA38GENICheterozygous521468119
203533699235336993CT42GENICheterozygous522337129
203533700035337001CT42GENICheterozygous521468120
203533701735337018AT40GENICheterozygous521468121
203533704535337046CT41GENICheterozygous521468122
203533714935337150GC34GENICheterozygous522337130
203533715535337156GA33GENICheterozygous522337131
203533716735337168CA38GENICheterozygous522337132
203533718735337188CT41GENICheterozygous521468123
203533719735337198GT47GENICheterozygous521468124
203533725135337252AG51GENICheterozygous522337133
203533725435337255AG50GENICheterozygous522337134
203533727735337278GA47GENICheterozygous522337135
203533728135337282GC49GENICheterozygous522337136
203535231935352320GC50GENICheterozygous521468125
203535313435353135GA44GENICheterozygous522337137
203535315835353159CT40GENICheterozygous521468126
203535320235353203CT45GENICheterozygous521468127
203535323035353231GA42GENICheterozygous521468128
203535979835359799GGT11GENICpossibly homozygous691665855
203536108035361081CT58GENICheterozygous521468129
203536110535361106GA61GENICheterozygous521468130