chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121538049815380499CA18GENIChomozygous139091636
121538074115380742C36GENIChomozygous139042666
121538240115382402GA20GENIChomozygous139091637
121538253715382538AG19GENIChomozygous139091638
121538350015383501GA20GENIChomozygous139091639
121538526915385270CT18GENIChomozygous139091640
121538585815385859AT17GENIChomozygous139091641
121538592715385928CG20GENIChomozygous139091642
121538701815387019TC11GENIChomozygous139091643
121538714215387143CT9GENIChomozygous139091644
121538761615387617CT30GENIChomozygous139091645
121538764815387649CT21GENIChomozygous139091646
121538803315388034GA21GENIChomozygous142320455
121538804715388048A22GENIChomozygous139042667
121538889115388892TC21GENIChomozygous139091647
121538896415388965CT20GENIChomozygous142320456
121538901015389011TC23GENIChomozygous139091648
121538924215389243GA24GENIChomozygous139091649
121538946515389466CT16GENIChomozygous139091650
121538959915389600TA23GENIChomozygous139091651
121538965915389660CT21GENIChomozygous139091652
121538996915389970GA19GENIChomozygous139091653
121539036115390362AG30GENIChomozygous139091654
121539039215390393TC28GENIChomozygous139091655
121539119415391195CT20GENIChomozygous139091656
121539156215391563AC22GENIChomozygous139091657
121539175515391756AG19GENIChomozygous139091658
121539182115391822TC17GENIChomozygous139091659
121539205715392061AAAA22GENIChomozygous139042668
121539230415392305CA18GENIChomozygous139091660
121539232415392325CT18GENIChomozygous139091661
121539347515393477TG18GENIChomozygous139042669
121539352315393524TC17GENIChomozygous139091662
121539353615393537AG16GENIChomozygous139091663
121539361915393620TA22GENIChomozygous139091664
121539392015393920CGC13GENICpossibly homozygous139042670
121539419315394194AG23GENIChomozygous139091665