chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13110274173110274174CT47GENIChomozygous114602328
13110274176110274177TG47GENIChomozygous114602330
13110274187110274188GT49GENIChomozygous114602332
13110274191110274192GA51GENIChomozygous114602334
13110274215110274216TG53GENIChomozygous114602336
13110274226110274227GT50GENIChomozygous114602338
13110274230110274231GT47GENIChomozygous114602340
13110274232110274233CT48GENIChomozygous114602342
13110274239110274240GT48GENIChomozygous114602344
13110274241110274242AT50GENIChomozygous114602346
13110274243110274244GT49GENIChomozygous114602348
13110274247110274248GT48GENIChomozygous114602350
13110274251110274252GT50GENIChomozygous114602352
13110275363110275364TG4GENIChomozygous118468804
13110282877110282877A26GENICheterozygous132895101
13110282878110282879CA26GENICheterozygous118468805
13110298271110298277TGCGCC7GENIChomozygous129097179
13110298281110298281GAG7GENIChomozygous129097180
13110298283110298285TC7GENIChomozygous129097181
13110298294110298294GGAGAAGGAGAGGGAGCAGGGGAGAGAGAGAGGGAGGGAGGGA6GENIChomozygous130419938
13110300827110300828A27GENIChomozygous129097184
13110300859110300860G30GENIChomozygous129097185
13110300865110300867TG30GENIChomozygous129097186
13110300874110300875G31GENIChomozygous129097187
13110300887110300887A39GENIChomozygous129097188
13110300901110300902T41GENIChomozygous129097189
13110300930110300931C42GENIChomozygous129097190
13110300976110300977G16GENIChomozygous129097191
13110301012110301013G26GENIChomozygous129097192
13110301073110301074C29GENIChomozygous129097193
13110301094110301094A26GENIChomozygous129097194
13110301116110301117A24GENIChomozygous129097195
13110301144110301144T16GENIChomozygous129097196