chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
389291378929138TG44GENIChomozygous111442506
389321608932161GA39GENIChomozygous119769725
389321618932162CT39GENIChomozygous119769727
389327188932719CT29GENICpossibly homozygous119769729
389329098932910TA36GENIChomozygous111442518
389346928934693AT27GENIChomozygous112329847
389354788935479TC30GENICpossibly homozygous119769731
389354858935486GT31GENICpossibly homozygous119769733
389364278936428TC12GENIChomozygous112329851
389366038936604AG33GENICpossibly homozygous119769735
389367898936790CT24GENIChomozygous119769737
389372928937293TC19GENIChomozygous111442525
389375098937510AG21GENIChomozygous111442526
389389248938925AG19GENIChomozygous111442529
389391348939135TC24GENIChomozygous119769739
389400028940003CA11GENIChomozygous119769741
389407478940748CT30GENIChomozygous111442531
389408488940849CT24GENICpossibly homozygous119769743
389423708942371CT17GENIChomozygous119769745
389423908942391AG22GENIChomozygous119769748
389424358942436AG32GENIChomozygous111442535
389426638942664GA16GENIChomozygous112329859
389427518942752TG26GENIChomozygous111442539
389429168942917GA31GENIChomozygous119769750
389438078943808TC20GENICpossibly homozygous111442540
389449828944983CT25GENICpossibly homozygous119769752
389451198945120GA25GENICpossibly homozygous119769754
389490018949002TC17GENIChomozygous111442543
389494428949443GA35GENICpossibly homozygous119769758
389495548949555GA28GENIChomozygous119769760
389496238949624CT18GENIChomozygous119769762
389500868950087GA31GENICpossibly homozygous111442544
389501808950181AG14GENIChomozygous111442546
389504718950472CT15GENIChomozygous111442547
389492028949203TG27GENICpossibly homozygous120076856