chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
166302415863024159GC22GENIChomozygous111840373
166305000763050008CG2GENIChomozygous112112511
166305000863050009GT2GENIChomozygous112210306
166305001563050016CA2GENIChomozygous112210308
166306310763063108AT15GENIChomozygous112112517
166306311363063114AT16GENIChomozygous112112519
166306321863063219GA4GENIChomozygous112220918
166313114463131145TG10GENIChomozygous111841019
166314139763141398AC16GENICheterozygous112220919
166323662263236623GT19GENIChomozygous111841383
166324348863243489GA9GENIChomozygous111841453
166326980863269809GT15GENIChomozygous111841519
166326980963269810GC15GENIChomozygous111841521
166326981063269811GT14GENIChomozygous111841523
166339403263394033TG22GENIChomozygous111841983
166339403363394034CT22GENIChomozygous111841985
166357413463574135TC11GENIChomozygous111842609
166358745263587453GT20GENIChomozygous111842643
166360371263603713AC9GENIChomozygous111842763
166362003463620035GT5GENIChomozygous112210316
166365226363652264CG24GENIChomozygous111843011
166365226563652266AC24GENIChomozygous111843013
166365227563652276TA25GENIChomozygous111843015
166370601963706020GC22GENIChomozygous111843069
166370602263706023GC23GENIChomozygous111843071
166370607963706080TA24GENIChomozygous111843073
166370608063706081TC23GENIChomozygous111843075
166370611363706114TC21GENIChomozygous111843077
166370611663706117CG21GENIChomozygous111843079
166370611763706118CG21GENIChomozygous111843081
166389095663890957CT17GENICheterozygous112068519
166389351663893517AG22GENIChomozygous112012937
166389352763893528TC22GENIChomozygous112012939
166389353963893540TG22GENIChomozygous112068521
166394604463946045TC17GENIChomozygous111843611
166396835463968355GA18GENIChomozygous112220920
166404690464046905CA16GENICheterozygous112220921