chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
36219072662190727TC20GENIChomozygous111589060
36219210662192107CT14GENIChomozygous111589061
36219268962192690GA13GENIChomozygous111589062
36219269062192691TC13GENIChomozygous111589063
36219311062193111AG27GENIChomozygous111589064
36219318662193187TG21GENIChomozygous111589065
36219333362193334CA9GENIChomozygous111589066
36219365762193658TC13GENIChomozygous111589068
36219398162193982CT16GENIChomozygous111589069
36219404862194049GA23GENIChomozygous111589070
36219431962194320GA19GENIChomozygous125825025
36219486962194870CT17GENIChomozygous111589074
36219512262195123GA8GENIChomozygous111589075
36219513262195133CT6GENIChomozygous111589076
36219567762195678TC20GENIChomozygous111589077
36219618062196181TC16GENIChomozygous111589079
36219622362196224TC15GENIChomozygous111589080
36219652462196525GA12GENIChomozygous111589081
36219655362196554AC8GENIChomozygous111589082
36219657962196580AT14GENIChomozygous111589083
36219708662197087GA11GENIChomozygous111589084
36219721262197213AC7GENIChomozygous111589085
36219748562197486AG19GENIChomozygous111589086
36219838162198382GA7GENIChomozygous111589087
36219842562198426AG12GENIChomozygous111589088
36219907762199078AC23GENICheterozygous111589089
36219913862199139TC27GENIChomozygous111589090
36219926762199268GT27GENIChomozygous111589091
36219988762199888GA29GENIChomozygous111589093
36219996962199970CT28GENIChomozygous111589094
36220050662200507GA15GENIChomozygous111589095