chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1160494303160494304GA38GENIChomozygous60916926
1160494775160494776CT32GENIChomozygous61771942
1160496451160496452CT34GENIChomozygous61771944
1160497538160497539A-23GENIChomozygous61771946
1160497925160497926GC26GENIChomozygous61771948
1160498166160498167AC20GENIChomozygous60916932
1160498368160498369CG22GENIChomozygous60916933
1160498393160498394TG22GENIChomozygous61771950
1160499251160499253AC--3GENICheterozygous62270459
1160499345160499346TC21GENIChomozygous61771954
1160506758160506759CCCCA5GENIChomozygous60916959
1160510042160510043TC31GENIChomozygous60916965
1160510134160510135CT22GENIChomozygous61771956
1160510635160510636TC23GENIChomozygous60916967
1160512239160512240AG26GENIChomozygous60916969
1160513655160513656AG28GENIChomozygous61771958
1160514414160514415TG22GENIChomozygous62270463
1160514423160514425TG--21GENIChomozygous61771960
1160514756160514757GGT12GENIChomozygous60916974
1160515334160515335AAATG27GENIChomozygous60916977
1160515805160515809GTGT----15GENICheterozygous61547208
1160515807160515809GT--15GENICpossibly homozygous61547209
1160516090160516091CT26GENIChomozygous60916979
1160517225160517226CT20GENIChomozygous61771962
1160517518160517519GA28GENIChomozygous61771964
1160517649160517651GA--25GENIChomozygous61771966
1160518432160518433TC26GENIChomozygous61771968
1160518677160518678GA24GENIChomozygous60916983
1160518701160518702TC25GENIChomozygous60916984
1160518900160518901TTA17GENICpossibly homozygous60916985
1160518907160518908TA25GENIChomozygous60916986
1160519208160519209TTCAAA21GENIChomozygous61771970