chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1197779462197779463AG19GENIChomozygous61682069
1197779599197779600AT26GENIChomozygous61581204
1197779616197779617TC19GENIChomozygous61581205
1197779666197779681TAACTCAGCCCTAGC---------------6GENIChomozygous61797863
1197779761197779762GT22GENIChomozygous61581206
1197780038197780039AG28GENIChomozygous61040768
1197780103197780104TC27GENIChomozygous61040769
1197782789197782790CT38GENICheterozygous61581207
1197783194197783195GC41GENIChomozygous61040777
1197783790197783807AAAAAAAAAAAAAAAAA-----------------22GENIChomozygous61797865
1197784440197784441GT41GENIChomozygous61797867
1197786013197786015TT--22GENICpossibly homozygous61797869
1197787720197787721GA20GENIChomozygous61040782
1197787893197787894CT37GENIChomozygous61797871
1197789290197789291CT38GENIChomozygous61797873
1197789774197789775TC35GENIChomozygous61040783
1197791785197791786CCTT10GENICheterozygous61040785
1197791786197791787T-10GENICheterozygous61581209
1197792095197792096TC31GENIChomozygous61040787
1197793841197793842TTTA23GENIChomozygous61797875
1197795632197795633AG22GENIChomozygous61797877
1197797106197797107TA26GENIChomozygous61040795
1197797239197797240GT22GENIChomozygous61797879
1197797715197797716GA39GENIChomozygous61797881
1197797775197797776CT48GENIChomozygous61040797
1197800327197800328AG29GENIChomozygous61040800
1197800406197800407CT32GENIChomozygous61040801
1197801953197801954CT26GENIChomozygous61040806
1197802718197802719TG34GENIChomozygous61040808
1197803867197803868TC28GENIChomozygous61040812
1197805067197805068AAT19GENIChomozygous61797883
1197805870197805871GA28GENIChomozygous61797885
1197805910197805911GGA16GENICheterozygous61040825
1197805990197805991AG29GENIChomozygous61040826