chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1222529786222529787GA19GENIChomozygous108546821
1222535423222535423G27GENICpossibly homozygous127486169
1222541441222541442CA27GENIChomozygous108546825
1222543119222543120TC12GENIChomozygous108546827
1222544499222544504AGACT10GENIChomozygous127486170
1222545124222545125AG16GENIChomozygous108546829
1222545750222545751CT29GENICpossibly homozygous108546830
1222546939222546940G11GENIChomozygous127486171
1222549947222549948GA23GENIChomozygous108546832
1222551617222551618GA21GENIChomozygous108546834
1222554182222554183AT20GENICheterozygous129860469
1222555784222555785GT15GENIChomozygous108546836
1222561018222561019AG22GENIChomozygous108546838
1222561446222561446A14GENIChomozygous127486172
1222561499222561500GC18GENIChomozygous108546840
1222564566222564567AG21GENIChomozygous108546842
1222565786222565786AAAAC16GENICpossibly homozygous127486173
1222565993222565994GA31GENIChomozygous108546844
1222566638222566639TG18GENIChomozygous108546846
1222566847222566848AG12GENIChomozygous108546848
1222570007222570008TG14GENIChomozygous127578189
1222571183222571184CT28GENIChomozygous108546850
1222573702222573702AAC25GENIChomozygous127486175
1222574203222574228GAGAGAGAGAGAGAGAGAGAGAGAG10GENICpossibly homozygous127486176
1222577637222577638GT5GENICheterozygous108546854
1222588180222588181A18GENIChomozygous127486177
1222576158222576158A4GENIChomozygous129845107