chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13110274173110274174CT38GENIChomozygous114602328
13110274176110274177TG37GENIChomozygous114602330
13110274187110274188GT40GENIChomozygous114602332
13110274191110274192GA39GENIChomozygous114602334
13110274215110274216TG39GENIChomozygous114602336
13110274226110274227GT41GENIChomozygous114602338
13110274230110274231GT41GENIChomozygous114602340
13110274232110274233CT41GENIChomozygous114602342
13110274239110274240GT42GENIChomozygous114602344
13110274241110274242AT44GENIChomozygous114602346
13110274243110274244GT45GENIChomozygous114602348
13110274247110274248GT45GENIChomozygous114602350
13110274251110274252GT44GENIChomozygous114602352
13110275363110275364TG4GENIChomozygous118468804
13110282877110282877A21GENICheterozygous132895101
13110282878110282879CA21GENICpossibly homozygous118468805
13110298271110298277TGCGCC5GENIChomozygous129097179
13110298281110298281GAG5GENIChomozygous129097180
13110298283110298285TC5GENIChomozygous129097181
13110298294110298294GGAGAAGGAGAGGGAGCAGGGGAGAGAGAGAGGGAGGGAGGGA5GENIChomozygous130419938
13110300827110300828A14GENIChomozygous129097184
13110300859110300860G18GENIChomozygous129097185
13110300865110300867TG18GENIChomozygous129097186
13110300874110300875G21GENIChomozygous129097187
13110300887110300887A22GENIChomozygous129097188
13110300901110300902T20GENIChomozygous129097189
13110300930110300931C21GENIChomozygous129097190
13110300976110300977G14GENIChomozygous129097191
13110301012110301013G26GENIChomozygous129097192
13110301073110301074C28GENIChomozygous129097193
13110301094110301094A27GENIChomozygous129097194
13110301116110301117A21GENIChomozygous129097195
13110301144110301144T13GENIChomozygous129097196