chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2243703066243703067CT32GENIChomozygous60087636
2243703850243703851AC18GENICheterozygous59472310
2243703891243703892AG23GENIChomozygous59472311
2243703899243703900GA24GENIChomozygous60087637
2243704231243704232GT30GENICheterozygous59950389
2243704413243704414AC22GENIChomozygous59472313
2243704457243704458AAC15GENICheterozygous60087638
2243704677243704678GA37GENICpossibly homozygous59472315
2243705186243705189GAA---2GENIChomozygous59472316
2243705196243705197CA2GENIChomozygous59472317
2243705198243705199TA2GENIChomozygous59472318
2243705201243705202CG2GENIChomozygous59472319
2243705203243705204AAG2GENIChomozygous59472320
2243705298243705299TTA23GENIChomozygous59472321
2243706074243706075AG38GENIChomozygous59472322
2243706468243706469AG39GENIChomozygous59472323
2243707930243707931TC38GENIChomozygous59472326
2243708087243708088GC35GENIChomozygous59472327
2243709284243709288CTCT----7GENIChomozygous60087639
2243713323243713324C-38GENIChomozygous59472333
2243713389243713390C-31GENIChomozygous59472334
2243705173243705174AG4GENICheterozygous60175325
2243705192243705193CA3GENICheterozygous59777682