chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------3GENIChomozygous724099059
85378107053781071CT15GENICpossibly homozygous590440262
85378121053781211AG2GENIChomozygous590440263
85378133353781334AG8GENICpossibly homozygous590440264
85378146653781467AG8GENIChomozygous590440265
85378180553781806AG13GENIChomozygous590440266
85378193153781932TTTA3GENICheterozygous724099060
85378200853782013GTTTG-----8GENIChomozygous724099063
85378241353782414CT3GENIChomozygous590440267
85378260753782608TC13GENICpossibly homozygous590440268
85378277053782771GA7GENICpossibly homozygous590440269
85378331953783320AG7GENIChomozygous590440270
85378340253783403T-4GENIChomozygous724099064
85378373853783739GT10GENICpossibly homozygous590440271
85378379353783794TC8GENIChomozygous590440272
85378404853784049TC8GENIChomozygous590440273
85378550553785506T-2GENIChomozygous724099065