chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2189841521189841522TC37GENIChomozygous110172114
2189841629189841630TC27GENIChomozygous110172115
2189845059189845060CT32GENIChomozygous110805119
2189845692189845693GA24GENICpossibly homozygous110805120
2189845696189845697AG24GENICheterozygous120155251
2189846796189846797GA18GENIChomozygous110805121
2189847825189847826CT17GENIChomozygous110805122
2189848559189848560AG20GENIChomozygous110172119
2189848577189848578CA27GENIChomozygous110805123
2189849730189849731AG32GENIChomozygous110805124
2189850481189850482GA30GENIChomozygous110805126
2189850600189850601GC32GENIChomozygous110805127
2189851040189851041CA47GENIChomozygous110805128
2189851056189851057GA40GENIChomozygous110805129
2189851852189851853TC38GENIChomozygous110805130
2189852164189852165GT25GENIChomozygous110805131
2189852386189852387GA26GENIChomozygous110805132
2189854130189854131CT29GENIChomozygous110805133
2189854287189854288CG41GENIChomozygous110172123