chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157382773157382774GC41GENIChomozygous112906055
4157386262157386263TA44GENICheterozygous113062874
4157388743157388744TG41GENIChomozygous112906057
4157390807157390808AG21GENICheterozygous112906059
4157390811157390812AG20GENICheterozygous112906061
4157390820157390821TC20GENICheterozygous112906063
4157390826157390827GA22GENICheterozygous112906065
4157392261157392262GA36GENIChomozygous112906067
4157394855157394856AG24GENIChomozygous112906069
4157394856157394857AG24GENIChomozygous112906071
4157396167157396168GA29GENICpossibly homozygous112906073
4157397875157397876CT22GENIChomozygous112906075
4157399492157399493TC40GENIChomozygous112906077
4157399850157399851CA38GENIChomozygous112906079
4157400365157400366GA26GENIChomozygous112906081
4157400388157400389CA23GENIChomozygous112906083
4157400419157400420TC19GENIChomozygous112906085
4157401383157401384AG56GENICheterozygous112906087
4157401384157401385CT56GENICheterozygous112906089
4157401432157401433CA15GENICheterozygous112906091
4157401440157401441CT46GENICheterozygous113062876
4157402357157402358AG34GENIChomozygous112906093
4157403131157403132TA35GENICpossibly homozygous112906095
4157403947157403948TC33GENIChomozygous112906097
4157404786157404787CG42GENIChomozygous112906099
4157405666157405667GA40GENIChomozygous112906101
4157407511157407512AC31GENIChomozygous112906103
4157407709157407710CT62GENIChomozygous112906105
4157408171157408172CT29GENIChomozygous112906107