chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142093574420935745TC57GENICpossibly homozygous795646231
142093605820936059TG51GENIChomozygous795646232
142093631120936312AG21GENICpossibly homozygous795646233
142093654320936544GA44GENICpossibly homozygous795646234
142093783520937836TG33GENICpossibly homozygous795646235
142093785520937856TA21GENICpossibly homozygous795646236
142094164320941644AG16GENIChomozygous795646237
142094166320941664GC16GENIChomozygous795646238
142094170220941703CA12GENIChomozygous795646239
142094170520941706GA12GENIChomozygous795646240
142094208520942086CA20GENIChomozygous795646241
142094214020942141CG31GENIChomozygous795646242
142094223220942233CA28GENIChomozygous795646243
142094600720946008CT43GENIChomozygous795646244
142094898520948986GC32GENIChomozygous795646245
142094898920948990TA31GENIChomozygous795646246
142094899820948999TA35GENIChomozygous795646247
142094900620949007AT34GENIChomozygous795646248
142094900820949009GC31GENIChomozygous795646249
142095117220951173TA64GENICheterozygous795646250
142095164820951649AG42GENIChomozygous795646251