chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1276241587276241588GA25GENIChomozygous108658664
1276243283276243284AG43GENIChomozygous108658665
1276245411276245412TC56GENIChomozygous108658669
1276254206276254207GA41GENIChomozygous108658671
1276255420276255421TG39GENIChomozygous108658677
1276255421276255422TC38GENIChomozygous108658678
1276260068276260069TC59GENIChomozygous108658683
1276261085276261086AG55GENIChomozygous108658684
1276261843276261844TC51GENIChomozygous108658686
1276265180276265181TC54GENIChomozygous108658687
1276265303276265304CA58GENIChomozygous108658688
1276265321276265322CT59GENIChomozygous108658689
1276270206276270207GA37GENIChomozygous108658690
1276270517276270518TC21GENIChomozygous108658691
1276270635276270636CT32GENIChomozygous108658692
1276270839276270840AG24GENIChomozygous108658693
1276270901276270902GA33GENIChomozygous108658694
1276271015276271016CT28GENIChomozygous108658695
1276272214276272215GA28GENIChomozygous108658696
1276275555276275556TC23GENIChomozygous108658698
1276275890276275891GA24GENIChomozygous108658699
1276275943276275944TC33GENIChomozygous108658700
1276277149276277150CG29GENIChomozygous108803315
1276277150276277151AC29GENIChomozygous120477611
1276278722276278723GA38GENIChomozygous108658703
1276280929276280930GA11GENIChomozygous108658704
1276283913276283914TC21GENIChomozygous108658705
1276284730276284731TC36GENIChomozygous108658706
1276285206276285207CA22GENIChomozygous108658707
1276286320276286321GC29GENIChomozygous108658708
1276286321276286322CA29GENIChomozygous109033122