chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144313347643133477GA42GENIChomozygous113441182
144313348843133489GA45GENIChomozygous113441184
144313378843133789AG52GENIChomozygous113441188
144313383343133834GT51GENIChomozygous113592671
144313434743134348AC35GENIChomozygous113441190
144313448043134481AC46GENIChomozygous113441192
144313493743134938GA58GENIChomozygous113441194
144313497443134975CA56GENIChomozygous113441196
144313513443135135CG31GENIChomozygous113441198
144313520043135201AG44GENIChomozygous113441200
144313529243135293GA57GENIChomozygous113441202
144313555743135558CT45GENIChomozygous113441204
144313559243135593AG49GENIChomozygous113441206
144313590643135907CT55GENIChomozygous113441208
144313666843136669GA47GENIChomozygous113441210
144313670743136708AG63GENIChomozygous113441212
144313689343136894TC57GENIChomozygous113441214
144313701043137011GC52GENIChomozygous113441216
144313794243137943CT44GENIChomozygous113441218
144313804643138047GA39GENIChomozygous113441220
144313842843138429TA44GENIChomozygous113441222
144313905343139054CT45GENIChomozygous113441224
144313913643139137TC42GENIChomozygous113441226
144313949543139496GA44GENIChomozygous113441228
144314058543140586GA35GENIChomozygous113441230
144314059743140598TC35GENIChomozygous113441232
144314055043140552TA31GENICheterozygous131144318
144314211043142111TG47GENIChomozygous118690905
144313607543136077TG34GENIChomozygous129151699
144313680843136808AC45GENIChomozygous129151700
144313684043136840GG48GENIChomozygous129151701
144313843843138438CTA38GENIChomozygous129151702
144313924943139249C48GENIChomozygous129151703
144314027243140273C38GENIChomozygous129151704
144314181643141816C29GENICpossibly homozygous129151705
144313827543138276GT37GENICpossibly homozygous114121711
144314356643143567AG28GENIChomozygous113441234
144314267343142673G22GENIChomozygous129151706