chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7240097472400975TG20GENICheterozygous45147018
X7240481572404816TG8GENICpossibly homozygous45147019
X7242411572424116G-18GENIChomozygous45147020
X7242752372427524CA12GENIChomozygous45147021
X7243195772431958AAG19GENIChomozygous45147022
X7243196072431961AAG19GENIChomozygous45147023
X7244102772441028TA11GENICheterozygous45147024
X7244439672444397C-19GENIChomozygous45147025
X7244506872445069G-9GENIChomozygous45147026
X7244935472449355GGAA10GENIChomozygous45147027
X7244940072449401C-2GENIChomozygous45147028
X7245577372455775GA--9INTERGENIChomozygous45147029
X7245637472456375GT14INTERGENIChomozygous45147030
X7248941472489415GGCT7INTERGENIChomozygous45147031
X7249287072492871AT27INTERGENICheterozygous45147032
X7249287872492879AG26INTERGENICheterozygous45147033
X7249288272492883T-23INTERGENICheterozygous45147034
X7250495172504952AG16GENICpossibly homozygous45147035
X7250954772509548CCA8GENIChomozygous45147036
X7251088072510881T-4GENICheterozygous45147037