chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98389719483897194A4GENICheterozygous138471187
98389719483897195GA4GENICheterozygous140901749
98389720283897203TC7GENICheterozygous140901750
98389721683897217TC9GENICheterozygous143416356
98389719883897199TA5GENICheterozygous403731082
98389719883897199T5GENICheterozygous403731083
98389720183897202TC5GENICheterozygous138615547
98389720583897206TC7GENICheterozygous138615548
98389720983897210TC7GENICheterozygous138615549
98389721483897215TC8GENICheterozygous138615550
98389720683897207TC8GENICheterozygous143416354
98389721083897211TC8GENICheterozygous143416355
98389721683897217T9GENICheterozygous403731084
98389721983897219C9GENICheterozygous138471189
98389722083897221TC10GENICheterozygous143416357
98389943583899436C25GENICheterozygous138471190
98392394483923945G16GENICheterozygous403268991
98392394483923945GC16GENICheterozygous403268992
98398774183987742A29GENICpossibly homozygous403268993
98398774183987742AG29GENICheterozygous403268994