chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101461976314619764TC73GENIChomozygous116496775
101462229614622297AT58GENIChomozygous116496783
101462239214622393CT58GENIChomozygous116737098
101462321114623212TC79GENIChomozygous116737099
101462361414623615GA63GENICheterozygous131100191
101462375214623753CA97GENICheterozygous118030764
101462362814623629CG60GENICheterozygous118062928
101462363914623640TC61GENICheterozygous118030758
101462371914623720AG92GENICheterozygous118030760
101462372414623725GA94GENICheterozygous118030762
101462370114623702CA80GENICheterozygous123312801
101462370314623704GT81GENICheterozygous123312802
101462370414623705TC81GENICheterozygous123312803
101462375514623756TC101GENICheterozygous118030766
101462380814623809CT122GENICheterozygous118030767
101462395514623956GA75GENICheterozygous118030769
101462398014623981AT75GENICheterozygous118030771
101462399214623993TC81GENICheterozygous117982469
101462400414624005GA75GENICheterozygous118030773
101462406814624069CA81GENICheterozygous118030775
101462408014624081TG82GENICheterozygous118030776
101462417914624180CT65GENICheterozygous118114054
101462420114624202AT56GENICheterozygous123312804
101462420314624204TG58GENICheterozygous123312805
101462531914625320GC57GENIChomozygous116737100
101462574814625749TC55GENIChomozygous116496791
101462734714627347CA63GENIChomozygous128790754
101462750414627504CCAGCAATGC56GENIChomozygous128790755
101462767714627678AT62GENIChomozygous116737101
101463721414637215A57GENIChomozygous128790759
101463726214637262T56GENIChomozygous128790760
101463756914637569TG48GENICpossibly homozygous128790761
101463926714639268GT58GENIChomozygous116737105
101462793714627938CT51GENIChomozygous116737102
101463125514631256GA68GENIChomozygous117408032
101463238814632389AC53GENIChomozygous116496809
101463265114632652CA77GENIChomozygous116737103
101463770514637706GA44GENIChomozygous116737104
101463128214631283CT60GENIChomozygous116994688