chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1524643162464317TG34GENIChomozygous143604424
1524651922465192ACTC40GENIChomozygous143600248
1524656752465676AT44GENIChomozygous143604425
1524660722466073AT39GENIChomozygous143604426
1524661462466147GA29GENIChomozygous143604427
1524665812466582AG51GENIChomozygous143604428
1524671862467187CT33GENIChomozygous143604429
1524683722468373TC28GENIChomozygous143604430
1524685472468548CG37GENICpossibly homozygous143604431
1524688622468863AC44GENIChomozygous143604432
1524692122469213CA54GENIChomozygous143604433
1524695792469580TC48GENIChomozygous143604434
1524696162469617GA44GENIChomozygous143604435
1524714312471432A38GENIChomozygous143600249
1524722982472299A40GENIChomozygous143600250
1524724522472453CT42GENIChomozygous143604436
1524727422472743CT54GENIChomozygous143604437
1524733372473338CT48GENIChomozygous143604438
1524736182473619GA43GENIChomozygous143604439
1524737052473706AT51GENIChomozygous143604440
1524662262466227AG14GENIChomozygous139653171
1524757612475762GA36GENIChomozygous143604441
1524766772476678AG64GENIChomozygous139653174
1524767432476744TC50GENIChomozygous139653175
1524662542466255CT15GENIChomozygous404092869