chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123704015337040154CT52GENIChomozygous115319400
123704016737040168AG50GENIChomozygous115319402
123704022537040226CA45GENIChomozygous115319404
123704128037041281GA66GENIChomozygous115319406
123704129137041292GA64GENIChomozygous115319408
123704181237041813AG55GENIChomozygous115319410
123704260737042608GC63GENIChomozygous115319412
123704261937042620TC60GENIChomozygous115319414
123704275537042756TC82GENIChomozygous115319416
123704359137043592AG66GENIChomozygous115319418
123704405737044058CT59GENIChomozygous115319420
123704472737044728GA52GENIChomozygous115319422
123704488437044885AG64GENIChomozygous115319424
123704578137045782TC72GENIChomozygous115319426
123704580537045806AG73GENIChomozygous115319428
123704604537046046GA67GENIChomozygous115319430
123704629237046293TC68GENIChomozygous115319432
123704629437046295TA69GENIChomozygous115319434
123704630337046304TC69GENIChomozygous115319436
123704631237046313GA70GENIChomozygous115319438
123704639837046399CT32GENIChomozygous115319440
123704728537047286CA57GENICpossibly homozygous115319442
123704754137047542TC64GENIChomozygous115319444
123704759837047599GA58GENIChomozygous115319446
123704194037041940GA62GENIChomozygous128985564
123704464137044643CA47GENIChomozygous128985565
123704701137047011G49GENIChomozygous128985566
123704684037046840GGTTC4GENICheterozygous134441296
123704685237046852TTTTCC3GENIChomozygous134441297