chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121532503115325032CT16GENIChomozygous50072230
121532510915325110TTC26GENIChomozygous50072232
121532515915325160TC39GENIChomozygous50072234
121532530315325304CT39GENIChomozygous50072236
121532534515325346AG33GENIChomozygous50072238
121532571315325714CT26GENIChomozygous50072240
121532582415325825TTTTTTTCTTTCCTTTTTTCTTTTTTTCGGAGCTGGGGACTGAACCCAGGGCCTTATGCTTGCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCCTGTTAATAGTTTCTA14GENIChomozygous50504030
121532688215326892GAGAATGAAT----------29GENIChomozygous50504031
121532721215327213TC34GENIChomozygous50072248
121532777315327774AG17GENIChomozygous50072254
121532780015327801AAGCGCTTACCTAGGAAGCGCAAGGCCCTG6GENIChomozygous50533644
121532751615327522CACACA------19GENICheterozygous50533638
121532751815327522CACA----19GENICpossibly homozygous50533640
121532911615329117TG26GENIChomozygous50072260
121532964415329645TC35GENIChomozygous50072262
121533037515330376AG35GENIChomozygous50072264
121533130815331309GA25GENIChomozygous50072266
121533138215331383AAT15GENICpossibly homozygous50072268
121533138215331383AATT15GENICheterozygous50072270
121533148415331485CT31GENIChomozygous50072272
121533186015331862GG--5GENIChomozygous50072274
121533204915332050AG24GENIChomozygous50072278
121533205815332059TC23GENIChomozygous50072280
121533230915332310GA33GENIChomozygous50072282
121533267915332680AAGT25GENIChomozygous50072284
121533289315332894A-10GENIChomozygous50533646
121533296815332976CACACACA--------28GENICheterozygous50533648
121533297015332976CACACA------28GENICpossibly homozygous50533650
121533644115336451AAATAATAAC----------9GENIChomozygous50072355
121533715515337156TC25GENIChomozygous50072361
121533844815338449CT22GENIChomozygous50072363
121533870015338714GTGTGTGTGTGTGT--------------21GENICheterozygous50533654
121533870215338714GTGTGTGTGTGT------------21GENICheterozygous50533656