chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124034104740341048TC43GENIChomozygous50203281
124034105840341059GA41GENIChomozygous50203282
124034121340341214AC32GENIChomozygous50422620
124034198640341987T-11GENIChomozygous50203283
124034233840342339GA28GENIChomozygous50203284
124034242640342427AG27GENIChomozygous50203285
124034276040342761AG46GENIChomozygous50203286
124034310740343108GGT18GENIChomozygous50203287
124034998440349985GGCACACACA7GENIChomozygous50203304
124035438640354387GA21GENIChomozygous50422621
124035741540357419GCGT----10GENIChomozygous50203357
124035741740357425GTGCGCGG--------10GENIChomozygous50203358
124035742340357425GG--10GENIChomozygous50203359
124035744540357449TCTG----11GENIChomozygous50203363
124035746740357468TA13GENIChomozygous50203366
124035747740357478AC12GENICheterozygous50203367
124035747940357480TA10GENIChomozygous50203368
124035749640357497GA8GENIChomozygous50203369
124035750240357503AT5GENIChomozygous50203370
124035750540357506CA5GENIChomozygous50203371
124035750740357508GC5GENIChomozygous50203372
124035750940357510AT5GENIChomozygous50203373
124035751340357514GC5GENIChomozygous50203374
124035751740357518TA5GENIChomozygous50203375
124035752140357522AT5GENIChomozygous50203376
124035819940358200TTC16GENIChomozygous50203380
124035820640358207TTC18GENIChomozygous50203381
124035821040358211GGC18GENIChomozygous50203382
124035844340358444CG85GENICpossibly homozygous50203387
124035844540358446CG85GENIChomozygous50203388
124035892940358930AG34GENICheterozygous50203389
124035893540358936AG37GENICheterozygous50203390
124035897340358974AG46GENICheterozygous50203391
124036412140364122A-5GENIChomozygous50203393
124036413440364136AA--16GENICheterozygous50203394
124036477440364775CT24GENIChomozygous50203396
124036478240364783AC20GENIChomozygous50203397