chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75904731859047319AT12GENIChomozygous648987004
75905213859052142ACAC----8GENICheterozygous756472023
75905214059052142AC--8GENICpossibly homozygous756472024
75905309559053097TG--12GENICheterozygous756472025
75905647159056472CCTTTTT7GENICheterozygous756472026
75906325159063252AG9GENIChomozygous648987005
75906325359063254AC8GENIChomozygous648987006
75906325759063258TA9GENIChomozygous648987007
75906325859063259GA9GENIChomozygous648987008
75906326859063269GT9GENIChomozygous648987009
75906327459063275GT8GENIChomozygous648987010
75906328159063282AT9GENIChomozygous648987011
75906329359063294G-7GENIChomozygous756472028
75906331059063311AT5GENIChomozygous648987012
75906331359063314A-5GENIChomozygous756472029
75906331659063317AT5GENIChomozygous648987013
75906331759063318AT5GENIChomozygous648987014
75906332059063321CT5GENIChomozygous648987015
75906332459063325G-5GENIChomozygous756472030
75906332659063327G-4GENIChomozygous756472031
75906333659063337A-3GENIChomozygous756472032
75906333859063339GT3GENIChomozygous648987016
75906334659063347GT3GENIChomozygous648987017
75906334959063350CCTTTTCACTT3GENIChomozygous756472033
75906335459063355GT3GENIChomozygous648987018
75906335859063362GGAA----2GENIChomozygous756472034
75906336959063370AT1GENIChomozygous648987019
75906337459063378GAAG----2GENIChomozygous756472035
75906337959063380GT2GENIChomozygous648987020
75906338159063382GT2GENIChomozygous648987021
75906338259063383AT2GENIChomozygous648987022
75906338359063384AT2GENIChomozygous648987023
75906338559063386GT3GENIChomozygous648987024
75906338759063388GT3GENIChomozygous648987025
75906339159063392GT4GENIChomozygous648987026
75906368559063686TTAC6GENICheterozygous756472036
75906368559063686TTACAC6GENICheterozygous756472037