chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
388023458802346AG47GENIChomozygous111873240
388025818802582CG60GENIChomozygous111442251
388026798802680AC59GENIChomozygous111442252
388028618802862AG69GENIChomozygous111442253
388041468804147AG44GENIChomozygous111442255
388043348804335AG46GENIChomozygous111442256
388048898804890GA35GENIChomozygous111442257
388050588805059TC63GENIChomozygous111442258
388056868805687GA43GENIChomozygous111442259
388068258806826CA52GENIChomozygous111873242
388074768807477TC42GENIChomozygous111442261
388077278807728CT31GENICpossibly homozygous111873244
388080118808012TG44GENIChomozygous111442262
388084938808494TC35GENIChomozygous111442263
388087648808765TG54GENIChomozygous111442265
388096618809662TC61GENIChomozygous111442266
388098558809856AG43GENIChomozygous111442267
388098748809875TC42GENIChomozygous111442268
388120168812017GA43GENIChomozygous111442270
388125198812520GT53GENIChomozygous111442271
388134888813489CT49GENIChomozygous111442272
388152308815231GA52GENIChomozygous111873246
388170018817002TC55GENIChomozygous111442274
388171748817175GT65GENIChomozygous111873248
388183778818378GT59GENIChomozygous111442275
388196428819643GT42GENIChomozygous111442276
388207938820794TC42GENIChomozygous111873250
388218798821880AG39GENIChomozygous111442278
388234518823452TC36GENIChomozygous111442279
388236768823677CT24GENIChomozygous111442280
388269468826947TC31GENIChomozygous111442285
388099878809987C47GENIChomozygous127848033
388206388820638TTTGGT50GENIChomozygous127848036
388105108810511CT60GENIChomozygous119966673
388159548815955AC46GENICpossibly homozygous131334970
388242798824280AG49GENIChomozygous111442281
388249138824914AG42GENIChomozygous111442282
388267048826705CT40GENIChomozygous111442283
388268048826805TC38GENIChomozygous111442284
388243358824338GAA44GENIChomozygous131325043
388272028827203TC49GENIChomozygous111442286