chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
203153320431533205AG28INTERGENIChomozygous63459789
203153432331534324AT37INTERGENIChomozygous63459791
203155753931557540CT30INTERGENIChomozygous63459957
203155798931557990AG22INTERGENIChomozygous63459959
203155870431558705AG29INTERGENIChomozygous63459967
203156039931560400AT19INTERGENIChomozygous63599106
203155778131557782CT35INTERGENIChomozygous63599101
203155785231557853GC27INTERGENIChomozygous63599102
203155864431558645AG28INTERGENIChomozygous63599103
203155901131559012CT42INTERGENIChomozygous63599104
203155917831559179GA36INTERGENIChomozygous63599105
203156206731562068TG20INTERGENICpossibly homozygous63459971
203156217331562174CG18INTERGENICpossibly homozygous63723572
203156217631562177GC18INTERGENICheterozygous63599107
203156221231562213CG13INTERGENICheterozygous84997408
203156235031562351CG18INTERGENICheterozygous84979240
203156234731562348GC17INTERGENICheterozygous84979239
203156235331562354GC18INTERGENICheterozygous84979241
203156592231565923AG25INTERGENIChomozygous63599109
203156647631566477GC20INTERGENICheterozygous63599110
203156648431566485GC19INTERGENICheterozygous63459991
203156648831566489GC20INTERGENICpossibly homozygous63459993
203156777831567779AG20INTERGENIChomozygous63599111
203156852831568529CA21INTERGENIChomozygous63599112
203156906231569063AG31INTERGENIChomozygous63599113