chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46284511062845111GA15GENIChomozygous784847067
46284520362845204TC27GENIChomozygous784847068
46284632862846329TC23GENIChomozygous784847069
46284645262846453TC27GENIChomozygous784847070
46284713962847140CG23GENIChomozygous784847071
46284812462848125TG18GENICpossibly homozygous784847072
46284858362848584TC26GENIChomozygous784847073
46284869962848700CT28GENIChomozygous784847074
46284895762848958CA14GENIChomozygous784847075
46285100362851004TC20GENIChomozygous784847076
46285108962851090GA21GENICpossibly homozygous784847077
46285133962851340CT36GENIChomozygous784847078
46285195562851956CT22GENIChomozygous784847079
46285352662853527GA24GENIChomozygous784847080
46285422862854229CT35GENICheterozygous784847081
46285425662854257AC15GENICheterozygous784847082
46285427962854280TC10GENIChomozygous784847083
46285428662854287GA9GENIChomozygous784847084
46285429362854294CT9GENIChomozygous784847085
46285430962854310CT20GENIChomozygous784847086
46285440562854406AG20GENICpossibly homozygous784847087
46285449862854499AG20GENICheterozygous784847088
46285453462854535AC13GENIChomozygous784847089
46285453662854537AG13GENIChomozygous784847090
46285455162854552CT12GENIChomozygous784847091
46285564162855642TC14GENIChomozygous784847092
46285574862855749TC30GENIChomozygous784847093
46285584662855847CT25GENIChomozygous784847094
46285610262856103AG25GENIChomozygous784847095
46285629962856300CT26GENIChomozygous784847096
46285641062856411AC27GENIChomozygous784847097
46285641262856413AG27GENIChomozygous784847098
46285642262856423CT31GENIChomozygous784847099
46285643362856434CT29GENIChomozygous784847100
46285643462856435AG29GENIChomozygous784847101
46285674262856743GA18GENIChomozygous784847102
46285712262857123CT18GENIChomozygous784847103
46285719562857196CT20GENIChomozygous784847104
46285866962858670CT23GENIChomozygous784847105
46286016662860167CG20GENIChomozygous784847106