chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1243436630243436631CT24GENICheterozygous61928905
1243436674243436675CT29GENICheterozygous61928906
1243446399243446400GA40GENICheterozygous61139383
1243476657243476658GA25GENICheterozygous61928953
1243478358243478359GA41GENICheterozygous61928956
1243478519243478520AG49GENICheterozygous61928957
1243529255243529256GA21GENICheterozygous61139605
1243533502243533503GA26GENICheterozygous61139612
1243536916243536917AG11GENICheterozygous61139634
1243548009243548010CT25GENICheterozygous61929056
1243558805243558814TCAGGCAGC---------29GENICheterozygous61929072
1243558835243558836GA27GENICheterozygous61139678
1243566474243566475TA19GENICheterozygous61811663
1243597770243597771CG49GENICheterozygous61139764
1243602271243602272CA16GENICheterozygous61811686
1243609561243609562GT9GENICheterozygous61811699
1243610194243610195AT24GENICheterozygous61139803
1243610258243610259CT20GENICheterozygous61811701
1243614612243614613AG14GENICheterozygous61139816
1243615298243615299CG20GENICheterozygous61811704
1243618839243618840AG76GENICheterozygous61139832
1243619010243619012TT--38GENICheterozygous61811708
1243619463243619464TC40GENICheterozygous61811711
1243619657243619658TTCTC47GENICheterozygous61139833
1243619888243619889TC44GENICheterozygous61139834
1243620227243620228TA60GENICheterozygous61139835
1243647628243647629AG16GENICheterozygous61811730
1243660877243660878AG11GENICheterozygous61811734
1243692869243692870GA31GENICheterozygous61811753
1243693310243693311AG43GENICheterozygous61139993
1243695450243695451CT19GENICheterozygous61811756
1243708505243708506CA29GENICheterozygous61140015
1243708587243708588AC43GENICheterozygous61140016
1243711347243711348TA39GENICheterozygous61140024