chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4175820185175820186A38GENICheterozygous128107349
4175822912175822913TG16GENICheterozygous133618709
4175823031175823032GT12GENICheterozygous132070231
4175823064175823065GA15GENICheterozygous132070232
4175823072175823073CT15GENICheterozygous132070233
4175823087175823088GT19GENICheterozygous132070234
4175824899175824900CA7GENICheterozygous133547826
4175847750175847750T42GENIChomozygous128107358
4175858075175858076T30GENIChomozygous128107362
4175822889175822890CA19GENICheterozygous113406857
4175822897175822898AT18GENICheterozygous113406859
4175858104175858104T26GENIChomozygous128107363
4175858149175858150G23GENIChomozygous128107364
4175858152175858153C23GENIChomozygous128107365
4175858184175858185G22GENIChomozygous128107366
4175869536175869536TAAAACATGCTTTAAAGTCCTCAGTAAGTGGTATCTTTCCTGCAAGGATTAAGGATCAGTCACATTTCAAGAAAACTGAAGTTCAAAGTGCTAATACATATTGGTTACTCACAAAACACGAGGTTATCTCTTGTCAGGAGAGGTGAAGTGGTTCCTTCCACCTGACTGAAGGACATACCTACTGAGCAATTACACATCAAGTAGT37GENICpossibly homozygous128107373