chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5170637935170637936AC47GENIChomozygous114091226
5170638216170638217CT66GENIChomozygous114091228
5170638422170638423AG53GENICheterozygous114091230
5170638426170638427TC57GENICheterozygous114091232
5170642235170642236CG54GENICheterozygous114091234
5170648263170648264GT31GENICpossibly homozygous114091236
5170648284170648285GT29GENIChomozygous114091238
5170649226170649227GA2GENIChomozygous114091240
5170649407170649408GC12GENIChomozygous114091242
5170649427170649428CA22GENIChomozygous114091244
5170649443170649444GT25GENIChomozygous114091246
5170649708170649709TC2GENIChomozygous114091248
5170649743170649744AG7GENIChomozygous114091250
5170649936170649937GT28GENIChomozygous114091252
5170655373170655374CA10GENIChomozygous114091254
5170656622170656623CG7GENIChomozygous114091256
5170656795170656796TC39GENIChomozygous114091258
5170656873170656874AT22GENIChomozygous114091260
5170656875170656876TC22GENIChomozygous114091262
5170656990170656991TG2GENIChomozygous114091264
5170657083170657084CG29GENIChomozygous114091266
5170657139170657140CT41GENIChomozygous114091268
5170657181170657182TG36GENIChomozygous114091270
5170657194170657195AC38GENIChomozygous114091272
5170657268170657269GA7GENIChomozygous114091274
5170664144170664145TC44GENIChomozygous114091276
5170664189170664190CA49GENIChomozygous114091278
5170674951170674952TC34GENIChomozygous114091280
5170675156170675157AG38GENIChomozygous114091282
5170675189170675190CG22GENIChomozygous114091284
5170675240170675241CA33GENIChomozygous114091286
5170675473170675474TG14GENIChomozygous114091288
5170675623170675624TA78GENICheterozygous114091290
5170675624170675625TC78GENICheterozygous114091292