chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8121843219121843220AG20GENICpossibly homozygous53229730
8121843359121843360CT14GENIChomozygous53229731
8121843428121843429CT21GENICpossibly homozygous53229732
8121843478121843479AG20GENICpossibly homozygous53229733
8121843825121843826GA11GENICheterozygous53229734
8121844425121844426AC22GENICpossibly homozygous53229735
8121844635121844636TC7GENICheterozygous52855910
8121845798121845799GC26GENICpossibly homozygous52855916
8121846799121846800TA12GENICheterozygous53229736
8121846878121846879CT18GENICpossibly homozygous53229737
8121848181121848182CT12GENIChomozygous53229740
8121848295121848296AC14GENICheterozygous53229741