chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228396792228396793CT62GENIChomozygous109000685
1228397127228397128CT68GENIChomozygous109000686
1228397652228397653CA56GENIChomozygous109000687
1228397762228397763A63GENIChomozygous130834043
1228397848228397848A70GENIChomozygous132539328
1228397916228397917TC55GENIChomozygous109000688
1228397947228397947A45GENIChomozygous132539329
1228398595228398596TC52GENICpossibly homozygous109000689
1228398920228398921CT67GENIChomozygous109000690
1228399190228399191GA65GENIChomozygous109000691
1228399421228399422CT56GENICpossibly homozygous109000692
1228399556228399557TA43GENIChomozygous109000693
1228399575228399576TC40GENIChomozygous109000694
1228399576228399577GA39GENIChomozygous109000695
1228399714228399715TC38GENIChomozygous109000696
1228399964228399965AG64GENIChomozygous109000697
1228400111228400112CT67GENIChomozygous109000698
1228401400228401401CA48GENICpossibly homozygous109000699
1228402799228402800TC67GENIChomozygous109000700
1228405898228405899AG55GENIChomozygous109000701
1228406349228406350AG58GENIChomozygous109000702
1228408015228408016CG69GENIChomozygous109000703
1228409233228409234GT57GENIChomozygous109000704
1228409429228409430GA64GENIChomozygous109000705
1228409509228409510AG71GENIChomozygous109000706
1228414335228414336TG53GENICpossibly homozygous109000712
1228415875228415876TA37GENIChomozygous109000713
1228416211228416213TC27GENIChomozygous132539331
1228416213228416214CA27GENIChomozygous120683179
1228416579228416579T22GENICpossibly homozygous130834045
1228417609228417609CATGCACACATG44GENIChomozygous130834046
1228417747228417747T58GENIChomozygous132539332
1228419146228419146TTCT52GENIChomozygous130834048
1228419750228419751GT58GENIChomozygous109000715
1228420804228420808AAAG32GENIChomozygous132539333
1228421171228421172AG7GENIChomozygous109000716
1228421293228421294CT43GENIChomozygous109000717
1228421301228421302TG45GENIChomozygous109000718