chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4175821874175821875GA11GENICheterozygous130307587
4175823803175823804TA5GENICheterozygous130550432
4175824884175824885GA5GENICheterozygous131376701
4175824890175824891TC4GENICheterozygous131376702
4175824922175824923CT4GENICheterozygous130307589
4175824924175824925TG4GENICheterozygous130307590
4175824934175824935GA4GENICheterozygous130307591
4175824997175824998C3GENICheterozygous130299974
4175841819175841820AT1GENIChomozygous119360211
4175847750175847750T18GENIChomozygous128107358
4175858075175858076T20GENIChomozygous128107362
4175858104175858104T19GENIChomozygous128107363
4175858149175858150G12GENIChomozygous128107364
4175858152175858153C12GENIChomozygous128107365
4175858184175858185G8GENIChomozygous128107366
4175869536175869536TAAAACATGCTTTAAAGTCCTCAGTAAGTGGTATCTTTCCTGCAAGGATTAAGGATCAGTCACATTTCAAGAAAACTGAAGTTCAAAGTGCTAATACATATTGGTTACTCACAAAACACGAGGTTATCTCTTGTCAGGAGAGGTGAAGTGGTTCCTTCCACCTGACTGAAGGACATACCTACTGAGCAATTACACATCAAGTAGT15GENICpossibly homozygous128107373