chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101509998315099984AG32GENICheterozygous116497709
101509999715099998CT38GENICheterozygous116497711
101510000115100002CT37GENICheterozygous116497713
101510006415100065GA44GENICheterozygous116497715
101510010215100103CG16GENICheterozygous117120410
101510010315100104TA18GENICheterozygous117120412
101510010915100110GT21GENICheterozygous117120414
101510011015100111TG21GENICheterozygous117120416
101510011415100115TA23GENICheterozygous117120418
101510011715100118GA21GENICheterozygous117140274
101510030615100307CT50GENICheterozygous116737568
101510036815100369GA34GENICheterozygous116497717
101510037615100377TC35GENICheterozygous116497719
101510052815100529CT38GENICheterozygous117074910
101510057315100574TC35GENICheterozygous116497721
101510102115101022CT30GENIChomozygous116737569
101510210215102103CT41GENICheterozygous116497735
101510212015102121CA38GENICheterozygous116497737
101510214415102145AG44GENICheterozygous116497739
101510214915102150CT43GENICheterozygous116497741
101510215015102151AG43GENICheterozygous116497743
101510216215102163CT41GENICheterozygous116497745
101510225115102252AG43GENICheterozygous116497749
101510227315102274AG30GENICheterozygous116497751
101510230115102302AG26GENICheterozygous116497753