chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1276241587276241588GA18GENIChomozygous108658664
1276243283276243284AG24GENIChomozygous108658665
1276243849276243850AG2GENIChomozygous108658666
1276243859276243860GA11GENIChomozygous108658668
1276245411276245412TC20GENIChomozygous108658669
1276254206276254207GA16GENIChomozygous108658671
1276255420276255421TG13GENIChomozygous108658677
1276255421276255422TC13GENIChomozygous108658678
1276260068276260069TC35GENIChomozygous108658683
1276261085276261086AG22GENIChomozygous108658684
1276261458276261459GA22GENIChomozygous108658685
1276261843276261844TC36GENIChomozygous108658686
1276265180276265181TC24GENIChomozygous108658687
1276265303276265304CA32GENIChomozygous108658688
1276265321276265322CT32GENIChomozygous108658689
1276270206276270207GA18GENIChomozygous108658690
1276270517276270518TC26GENIChomozygous108658691
1276270635276270636CT24GENIChomozygous108658692
1276270839276270840AG29GENIChomozygous108658693
1276270901276270902GA34GENIChomozygous108658694
1276271015276271016CT44GENIChomozygous108658695
1276272214276272215GA35GENIChomozygous108658696
1276275128276275129GA34GENIChomozygous108658697
1276275555276275556TC16GENIChomozygous108658698
1276275890276275891GA36GENIChomozygous108658699
1276275943276275944TC37GENIChomozygous108658700
1276277149276277150CG29GENIChomozygous108803315
1276280929276280930GA19GENIChomozygous108658704
1276283913276283914TC26GENIChomozygous108658705
1276284730276284731TC26GENIChomozygous108658706
1276285206276285207CA39GENIChomozygous108658707
1276286320276286321GC22GENIChomozygous108658708
1276286321276286322CA22GENIChomozygous109033122
1276278620276278621AC4GENIChomozygous120477612
1276277150276277151AC29GENIChomozygous120477611