chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2187114527187114528AG59GENIChomozygous110166929
2187114784187114785TC52GENIChomozygous110166930
2187114917187114918AG63GENIChomozygous110166931
2187115561187115562AG59GENIChomozygous110166932
2187116861187116862AG71GENIChomozygous110166933
2187118980187118981GA69GENIChomozygous110166934
2187119480187119481GA70GENIChomozygous110166935
2187120335187120336GA53GENIChomozygous110166936
2187121209187121210AG70GENIChomozygous110166937
2187121900187121901AG59GENIChomozygous110166938
2187123110187123111CG49GENIChomozygous110166939
2187123947187123948CT62GENIChomozygous110166940
2187124170187124171GA64GENIChomozygous110166941
2187124695187124696GA66GENICpossibly homozygous110166942
2187125163187125164CT63GENIChomozygous110166943
2187126341187126342GA57GENIChomozygous110166944
2187127537187127538GA56GENIChomozygous110166945
2187129159187129160CT27GENIChomozygous110166946
2187129762187129763CT70GENIChomozygous110166947
2187130331187130332GA63GENIChomozygous110166948
2187130911187130912AG84GENIChomozygous110166949
2187134101187134102CG49GENIChomozygous110166950
2187121113187121114G71GENIChomozygous127716660