chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46284511062845111GA15GENIChomozygous112673357
46284520362845204TC27GENIChomozygous112673359
46284632862846329TC23GENIChomozygous112673361
46284645262846453TC27GENIChomozygous112673363
46284713962847140CG23GENIChomozygous112673365
46284812462848125TG18GENICpossibly homozygous112673367
46284858362848584TC26GENIChomozygous112673369
46284869962848700CT28GENIChomozygous112673371
46284895762848958CA14GENIChomozygous112673373
46285100362851004TC20GENIChomozygous112673375
46285108962851090GA21GENICpossibly homozygous112673377
46285133962851340CT36GENIChomozygous112673379
46285195562851956CT22GENIChomozygous112673381
46285352662853527GA24GENIChomozygous112673383
46285422862854229CT35GENICheterozygous113113651
46285425662854257AC15GENICheterozygous112673387
46285427962854280TC10GENIChomozygous112673389
46285428662854287GA9GENIChomozygous112673391
46285429362854294CT9GENIChomozygous112673393
46285430962854310CT20GENIChomozygous112673395
46285440562854406AG20GENICpossibly homozygous112673397
46285449862854499AG20GENICheterozygous112673399
46285453462854535AC13GENIChomozygous112673401
46285453662854537AG13GENIChomozygous112673403
46285455162854552CT12GENIChomozygous112673405
46285564162855642TC14GENIChomozygous112673407
46285574862855749TC30GENIChomozygous112673409
46285584662855847CT25GENIChomozygous112673411
46285610262856103AG25GENIChomozygous112673413
46285629962856300CT26GENIChomozygous112673415
46285641062856411AC27GENIChomozygous112673417
46285641262856413AG27GENIChomozygous112673419
46285642262856423CT31GENIChomozygous112673421
46285643362856434CT29GENIChomozygous112673423
46285643462856435AG29GENIChomozygous112673425
46285674262856743GA18GENIChomozygous112673427
46285712262857123CT18GENIChomozygous112673429
46285719562857196CT20GENIChomozygous112673431
46285866962858670CT23GENIChomozygous112673433
46286016662860167CG20GENIChomozygous112673435