chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
203533693635336937CA36GENICheterozygous45535764
203533700035337001CT37GENICheterozygous45535765
203533701735337018AT42GENICheterozygous45535766
203533704535337046CT59GENICheterozygous45535767
203533713735337138GC40GENICheterozygous45535768
203533714935337150GC44GENICheterozygous45625179
203533715535337156GA46GENICheterozygous45625180
203533716735337168CA51GENICheterozygous45625181
203533718735337188CT55GENICheterozygous45625182
203533719735337198GT54GENICheterozygous45625183
203533725135337252AG59GENICheterozygous45535769
203533725435337255AG61GENICheterozygous45535770
203533727735337278GA60GENICheterozygous45707096
203533728135337282GC61GENICheterozygous45707097
203533730035337301GA53GENICheterozygous45707098
203535231935352320GC22GENICheterozygous45535804
203535313435353135GA33GENICheterozygous45535808
203535315835353159CT46GENICheterozygous45535809
203535320235353203CT54GENICheterozygous45535810
203535323035353231GA44GENICheterozygous45535811
203535979835359799GGT10GENICpossibly homozygous45535884
203536108035361081CT73GENICheterozygous45535893
203536110535361106GA68GENICheterozygous45535894