chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101461976314619764TC12GENIChomozygous116496775
101462229614622297AT14GENIChomozygous116496783
101462239214622393CT10GENIChomozygous116737098
101462321114623212TC17GENIChomozygous116737099
101462361414623615GA24GENICheterozygous131100191
101462370114623702CA28GENICheterozygous123312801
101462370314623704GT28GENICheterozygous123312802
101462370414623705TC28GENICheterozygous123312803
101462375514623756TC36GENICheterozygous118030766
101462357714623577G23GENICheterozygous131088046
101462371914623720AG26GENICheterozygous118030760
101462372414623725GA27GENICheterozygous118030762
101462375214623753CA34GENICheterozygous118030764
101462380814623809CT39GENICheterozygous118030767
101462395514623956GA21GENICheterozygous118030769
101462398014623981AT19GENICheterozygous118030771
101462399214623993TC20GENICheterozygous117982469
101462406814624069CA21GENICheterozygous118030775
101462408014624081TG20GENICheterozygous118030776
101462417914624180CT24GENICheterozygous118114054
101462420114624202AT24GENICheterozygous123312804
101462420314624204TG25GENICheterozygous123312805
101462531914625320GC14GENIChomozygous116737100
101462574814625749TC12GENIChomozygous116496791
101462734714627347CA16GENIChomozygous128790754
101462750414627504CCAGCAATGC18GENIChomozygous128790755
101462767714627678AT22GENIChomozygous116737101
101462793714627938CT14GENIChomozygous116737102
101463125514631256GA20GENIChomozygous117408032
101463238814632389AC13GENIChomozygous116496809
101463265114632652CA14GENIChomozygous116737103
101463721414637215A11GENIChomozygous128790759
101463726214637262T14GENIChomozygous128790760
101463756914637569TG13GENIChomozygous128790761
101463770514637706GA12GENIChomozygous116737104
101463128214631283CT20GENIChomozygous116994688
101463926714639268GT9GENIChomozygous116737105