chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75904731859047319AT6GENIChomozygous558076047
75905214059052142AC--3GENICheterozygous705228222
75905647159056472CCTTTTT5GENICheterozygous705228223
75905647159056472CCTTTTCTTTTCT5GENICheterozygous705228224
75906325159063252AG10GENIChomozygous558076048
75906325359063254AC10GENIChomozygous558076049
75906325759063258TA10GENIChomozygous558076050
75906325859063259GA10GENIChomozygous558076051
75906326859063269GT12GENIChomozygous558076052
75906327459063275GT12GENIChomozygous558076053
75906328159063282AT14GENIChomozygous558076054
75906329359063294G-14GENIChomozygous705228225
75906331059063311AT10GENIChomozygous558076055
75906331359063314A-10GENIChomozygous705228226
75906331659063317AT10GENIChomozygous558076056
75906331759063318AT10GENIChomozygous558076057
75906332059063321CT10GENIChomozygous558076058
75906332459063325G-9GENIChomozygous705228227
75906332659063327G-9GENIChomozygous705228228
75906333659063337A-5GENIChomozygous705228229
75906333859063339GT4GENIChomozygous558076059
75906334659063347GT4GENIChomozygous558076060
75906334959063350CCTTTTCACTT6GENIChomozygous705228230
75906335459063355GT6GENIChomozygous558076061
75906335859063362GGAA----7GENIChomozygous705228231
75906336959063370AT6GENIChomozygous558076062
75906337459063378GAAG----8GENIChomozygous705228232
75906337959063380GT7GENIChomozygous558076063
75906338159063382GT6GENIChomozygous558076064
75906338259063383AT6GENIChomozygous558076065
75906338359063384AT6GENIChomozygous558076066
75906338559063386GT6GENIChomozygous558076067
75906338759063388GT6GENIChomozygous558076068
75906339159063392GT7GENIChomozygous558076069
75908289659082936GAGAGAGGGAGAGAGGGAGAGAGGGAGAGAGGGAGAGAGG----------------------------------------5GENICheterozygous705228233