chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171000258210002582TTTC30GENICheterozygous144171969
171000369710003698A22GENICheterozygous403406424
171000369710003698AG22GENICheterozygous403406425
171000373110003732AG42GENIChomozygous144181253
171000500510005005A40GENICpossibly homozygous144171970
171000722210007223TC51GENIChomozygous140052089
171000740710007407TGGCTCTCCTGGCCC54GENIChomozygous144171971
171000776710007768AG70GENIChomozygous140052091
171000823510008236GA54GENIChomozygous144181254
171000828510008286GA55GENIChomozygous144181255
171000851210008513T56GENIChomozygous144171972
171000871410008715TC53GENIChomozygous140052093
171000971710009718GA57GENIChomozygous144181256
171000985810009859GA58GENIChomozygous144181257
171001003110010032CT58GENIChomozygous140052097
171001031810010319CT49GENIChomozygous144181258
171001042610010427TC64GENIChomozygous144181259
171001086710010868AG51GENIChomozygous144181260
171001091910010920GA46GENIChomozygous144181261
171001099510010996AG55GENIChomozygous140052098
171001113010011131TC66GENIChomozygous140052099
171001141910011420AG49GENIChomozygous144181262
171001174110011742CT52GENIChomozygous144181263
171001189010011891CT60GENICpossibly homozygous144181264
171001202610012027AC53GENIChomozygous144181265
171001232910012329CTCCTCCAACAAAGCCACAC39GENICpossibly homozygous144171973
171001265810012659GA53GENIChomozygous144181266
171001283510012836CT59GENIChomozygous144181267
171001289110012892CT51GENIChomozygous144181268
171001309510013097AC47GENIChomozygous144171974
171001316610013167AG60GENIChomozygous144181269
171001336410013365GA55GENIChomozygous144181270
171001389810013899GT69GENIChomozygous144181271
171001418810014188GGGGT17GENIChomozygous144171975
171001534110015342GA59GENIChomozygous144181272
171001652410016525TC58GENIChomozygous144181273
171001737210017373CT67GENIChomozygous144181274
171001818410018185AG56GENIChomozygous144181275
171001361410013615AT43GENIChomozygous149097761
171000916410009165AG14GENICpossibly homozygous149097760