chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------18GENIChomozygous765504325
85378107053781071CT20GENIChomozygous664015252
85378121053781211AG22GENIChomozygous664015253
85378128753781288GGAAA22GENIChomozygous765504329
85378133353781334AG22GENIChomozygous664015254
85378146653781467AG22GENIChomozygous664015255
85378180553781806AG25GENIChomozygous664015256
85378193153781932TTTA23GENICheterozygous765504330
85378193153781932TTTTA23GENICpossibly homozygous765504331
85378200853782013GTTTG-----12GENIChomozygous765504333
85378241353782414CT19GENIChomozygous664015257
85378260753782608TC22GENIChomozygous664015258
85378277053782771GA15GENIChomozygous664015259
85378331953783320AG29GENIChomozygous664015260
85378340253783403T-21GENIChomozygous765504334
85378373853783739GT23GENIChomozygous664015261
85378379353783794TC23GENIChomozygous664015262
85378391753783918T-19GENIChomozygous765504335
85378391953783926TGCGTGT-------20GENIChomozygous765504336
85378404853784049TC19GENIChomozygous664015263
85378550553785506T-4GENIChomozygous765504337
85378552153785522CCTTTT6GENIChomozygous765504339