chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1205025130205025131C-7INTERGENIChomozygous61063885
1205025214205025215CT13INTERGENIChomozygous61063886
1205027765205027766CT9INTERGENICheterozygous61063887
1205027796205027799CCA---3INTERGENICheterozygous61063888
1205027798205027801AGT---4INTERGENICheterozygous61063889
1205027806205027807T-4INTERGENICheterozygous61063890
1205027819205027820T-5INTERGENICheterozygous61063891
1205027918205027919CA22INTERGENICpossibly homozygous61063892
1205028302205028303AG31INTERGENIChomozygous61063893
1205028332205028333A-2INTERGENIChomozygous61063894
1205029353205029354TC44INTERGENIChomozygous61063895
1205029550205029551G-24INTERGENIChomozygous61063896
1205029903205029907TACG----22INTERGENIChomozygous61063897
1205029914205029915GA23INTERGENICheterozygous61063898
1205029916205029917AG23INTERGENICheterozygous61063899
1205029935205029936TC25INTERGENICheterozygous61063900
1205029947205029948CT24INTERGENICpossibly homozygous61063901
1205029976205029977AT23INTERGENICheterozygous61063902
1205029976205029977AACTCT15INTERGENICheterozygous61063903
1205030233205030234CT36INTERGENIChomozygous61063904
1205030433205030434AT43INTERGENIChomozygous61063905