chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8121843219121843220AG23GENICpossibly homozygous53229730
8121843359121843360CT37GENIChomozygous53229731
8121843428121843429CT36GENIChomozygous53229732
8121843478121843479AG36GENIChomozygous53229733
8121843825121843826GA33GENIChomozygous53229734
8121844425121844426AC32GENIChomozygous53229735
8121844635121844636TC30GENIChomozygous52855910
8121845798121845799GC41GENIChomozygous52855916
8121846799121846800TA24GENIChomozygous53229736
8121846878121846879CT36GENIChomozygous53229737
8121847281121847282A-8GENIChomozygous53229738
8121847356121847357AT45GENICpossibly homozygous53229739
8121848181121848182CT41GENIChomozygous53229740
8121848295121848296AC29GENIChomozygous53229741