chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104593948445939485GC8GENICheterozygous51636547
104593949045939491GGA5GENICheterozygous51443545
104593956745939568A-22GENICheterozygous51636548
104593966845939669GGA13GENICpossibly homozygous51443548
104594046345940464AAT24GENIChomozygous51443550
104594126945941270AG22GENIChomozygous51443555
104594163645941637TC27GENIChomozygous51443556
104594271245942713AG31GENIChomozygous52052983
104594279945942800GA24GENIChomozygous52052985
104594290345942907TGTG----2GENICheterozygous51443560
104594437545944377CA--37GENIChomozygous51443564
104594467645944677GA58GENIChomozygous52052987
104594871745948722AAAAA-----38GENICpossibly homozygous51443571
104595005245950053GA45GENIChomozygous52052990
104595264045952641GT36GENIChomozygous52052992
104595339945953401AG--30GENICheterozygous51443582
104595559145955592GA20GENIChomozygous52052994
104595593645955937A-44GENIChomozygous51443584
104595700145957002AG24GENIChomozygous51443585
104595706245957063GA27GENIChomozygous52052996
104595816845958177CAGGACAGC---------6GENICheterozygous52052998
104595834945958353ATAC----15GENIChomozygous51874608
104595942545959426CT23GENICpossibly homozygous52053000
104595962045959621TC48GENICpossibly homozygous51443590