chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167395024973950250GA20GENIChomozygous64774568
167395067573950676CT12GENIChomozygous64584790
167395345973953460CT23GENICpossibly homozygous64584796
167395558073955581AG17GENIChomozygous64584805
167395611273956113CT23GENIChomozygous64774572
167395791573957916CT25GENIChomozygous64774574
167395874873958749AG20GENIChomozygous64584811
167395937873959379CT14GENIChomozygous64774578
167396168673961687AG15GENIChomozygous64584813
167396199273961993GA11GENIChomozygous64584816
167396328573963286CT20GENIChomozygous64774580
167396351673963517TC25GENIChomozygous64584819
167396371873963719AG22GENIChomozygous64584822
167396424373964244AT18GENIChomozygous64584825
167396446473964465CT14GENIChomozygous64584828
167396536473965365TC3GENIChomozygous64774588
167396553973965540AG6GENIChomozygous64774590
167396763773967638CT15GENIChomozygous64584837
167396890173968902AG17GENIChomozygous64584840
167416808674168087CT35GENIChomozygous64774592
167416953074169531AT23GENIChomozygous64774594
167416971874169719TG27GENIChomozygous64584860
167417039074170391GA23GENIChomozygous64774596
167417053074170531AC23GENIChomozygous64584863
167417155774171558TA36GENIChomozygous64584869
167417310074173101TA27GENIChomozygous64584875