chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101461976314619764TC21GENIChomozygous116496775
101462229614622297AT29GENIChomozygous116496783
101462239214622393CT31GENIChomozygous116737098
101462321114623212TC32GENIChomozygous116737099
101462375514623756TC36GENICheterozygous118030766
101462361414623615GA25GENICheterozygous131100191
101462371914623720AG33GENICheterozygous118030760
101462372414623725GA34GENICheterozygous118030762
101462375214623753CA35GENICheterozygous118030764
101462370114623702CA33GENICheterozygous123312801
101462370314623704GT33GENICheterozygous123312802
101462370414623705TC33GENICheterozygous123312803
101462380814623809CT50GENICheterozygous118030767
101462395514623956GA16GENICheterozygous118030769
101462406814624069CA17GENICheterozygous118030775
101462408014624081TG19GENICheterozygous118030776
101462531914625320GC23GENIChomozygous116737100
101462574814625749TC22GENIChomozygous116496791
101462734714627347CA27GENIChomozygous128790754
101462750414627504CCAGCAATGC35GENIChomozygous128790755
101462767714627678AT29GENIChomozygous116737101
101462793714627938CT32GENIChomozygous116737102
101463099214630992T10GENICheterozygous128790757
101463125514631256GA15GENIChomozygous117408032
101463238814632389AC16GENIChomozygous116496809
101463265114632652CA20GENIChomozygous116737103
101463721414637215A21GENIChomozygous128790759
101463726214637262T25GENIChomozygous128790760
101463756914637569TG22GENICpossibly homozygous128790761
101463770514637706GA20GENIChomozygous116737104
101463926714639268GT24GENIChomozygous116737105
101463128214631283CT19GENIChomozygous116994688