chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------2GENIChomozygous699100238
85378107053781071CT14GENICpossibly homozygous547419506
85378121053781211AG9GENIChomozygous547419507
85378133353781334AG7GENICheterozygous547419508
85378146653781467AG15GENICpossibly homozygous547419509
85378180553781806AG10GENIChomozygous547419510
85378200853782013GTTTG-----9GENIChomozygous699100239
85378241353782414CT16GENIChomozygous547419511
85378260753782608TC19GENICpossibly homozygous547419512
85378277053782771GA5GENIChomozygous547419513
85378331953783320AG17GENIChomozygous547419514
85378340253783403T-2GENICheterozygous699100240
85378373853783739GT14GENIChomozygous547419515
85378379353783794TC10GENIChomozygous547419516
85378404853784049TC9GENIChomozygous547419517
85378438353784384A-8GENICheterozygous699100241
85378550553785506T-2GENIChomozygous699100243