chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2230790000230790001AG24GENICpossibly homozygous59432905
2230790077230790078GA26GENICpossibly homozygous59432906
2230790377230790378CT14GENIChomozygous59432907
2230790527230790528AG8GENIChomozygous59432908
2230790540230790541AAT1GENIChomozygous59432909
2230791253230791254TTAA8GENIChomozygous59432910
2230791872230791873AG15GENIChomozygous59432911
2230794101230794102GGA4GENICheterozygous59432916
2230794220230794221AG14GENIChomozygous59432917
2230794590230794591G-5GENICheterozygous59432919
2230795546230795547TC11GENICpossibly homozygous59432923
2230795657230795658TC16GENIChomozygous59432924
2230796598230796599GA23GENICpossibly homozygous59432925
2230796732230796733AG28GENIChomozygous59432926
2230799442230799443AG19GENIChomozygous59432932
2230801382230801383CT23GENIChomozygous59432936