chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104492716044927161AG1GENIChomozygous545887003
104492861244928613GA15GENIChomozygous547729416
104493279244932793TC22GENICpossibly homozygous545887004
104493597044935971CT16GENIChomozygous547729417
104493614544936146GA4GENIChomozygous545887005
104493825844938259AG5GENICheterozygous545887006
104493825944938260AG6GENICheterozygous545887007
104493884744938848GA9GENICheterozygous547729418
104494024544940246CA22GENIChomozygous545887008
104494136044941361TC16GENIChomozygous545887009
104494277044942771TC26GENIChomozygous547729419
104494290544942906CT23GENIChomozygous545887010