chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
32160250921602510CT8GENIChomozygous111504119
32160258521602586GA15GENICheterozygous127977427
32160260621602607CA15GENICheterozygous111894917
32160262621602627GT22GENICheterozygous127977428
32160315621603157AG10GENIChomozygous111504121
32160350421603505GA19GENIChomozygous111504123
32160484621604847AG23GENIChomozygous111504132
32160505021605051AG17GENIChomozygous111504134
32160507621605077GT17GENIChomozygous111504135
32160548121605482TC18GENIChomozygous111504137
32160549521605496TC21GENIChomozygous111504139
32160549621605497GA21GENIChomozygous111504141
32160552621605527CA21GENIChomozygous111504142
32160609221606093GT24GENIChomozygous111504144
32160631321606314AG18GENIChomozygous111504146
32160682521606826AG20GENIChomozygous111504148
32160263421602634A24GENICheterozygous127859479
32160607221606075TCT23GENIChomozygous127859480
32160785021607851AG16GENIChomozygous111504150
32160861621608617GC22GENICheterozygous127977430
32160862121608624AAT20GENICheterozygous127859481
32160887521608876GA26GENICheterozygous112094863
32160946721609468TC18GENIChomozygous111504152