chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8128028359128028360TC32GENIChomozygous52884672
8128028481128028482CCTTTTA11GENIChomozygous52884673
8128029653128029654CCTT10GENIChomozygous52884674
8128029661128029662TTTTG14GENICpossibly homozygous52884675
8128029662128029663GGTT6GENICheterozygous52884676
8128029662128029663GGGTT6GENICheterozygous52884677
8128030090128030091TC28GENIChomozygous52884678
8128030446128030447TC30GENIChomozygous52884679
8128031132128031133GA46GENIChomozygous52884680
8128031353128031354CT32GENIChomozygous52884681
8128031364128031365CT33GENIChomozygous52884682
8128032203128032204GA24GENIChomozygous52884683
8128032444128032445TC39GENIChomozygous52884684
8128033460128033461AG31GENIChomozygous52884686
8128033467128033468TA29GENIChomozygous52884687
8128034345128034346AAT27GENICpossibly homozygous52884688
8128034693128034695CT--7GENIChomozygous52884689
8128034695128034696C-6GENIChomozygous52884691
8128034696128034699TTA---7GENIChomozygous52884692
8128034697128034699TA--6GENIChomozygous52884693
8128035400128035401AAC24GENIChomozygous52884694
8128035410128035411CCA27GENIChomozygous52884695
8128035473128035474GA37GENIChomozygous52884696
8128035655128035656TTGG24GENIChomozygous52884697
8128034346128034347AT29GENIChomozygous53064453