chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1276241587276241588GA16GENIChomozygous108658664
1276243283276243284AG14GENIChomozygous108658665
1276243849276243850AG3GENICheterozygous108658666
1276245411276245412TC21GENIChomozygous108658669
1276254206276254207GA24GENIChomozygous108658671
1276254456276254457GA22GENIChomozygous108658672
1276255420276255421TG6GENIChomozygous108658677
1276255421276255422TC6GENIChomozygous108658678
1276256646276256647CA25GENIChomozygous125329703
1276258702276258703GA11GENIChomozygous108658681
1276260068276260069TC28GENIChomozygous108658683
1276261085276261086AG23GENIChomozygous108658684
1276261458276261459GA27GENIChomozygous108658685
1276261843276261844TC28GENIChomozygous108658686
1276265180276265181TC17GENIChomozygous108658687
1276265303276265304CA17GENIChomozygous108658688
1276265321276265322CT10GENIChomozygous108658689
1276266304276266305GA27GENIChomozygous125329704
1276267355276267356CT26GENIChomozygous125329705
1276269729276269730CA9GENIChomozygous125329706
1276270206276270207GA21GENIChomozygous108658690
1276270517276270518TC16GENIChomozygous108658691
1276270635276270636CT23GENIChomozygous108658692
1276270839276270840AG17GENIChomozygous108658693
1276270901276270902GA17GENIChomozygous108658694
1276271015276271016CT11GENIChomozygous108658695
1276272214276272215GA32GENIChomozygous108658696
1276275128276275129GA29GENIChomozygous108658697
1276278722276278723GA14GENIChomozygous108658703
1276280929276280930GA14GENIChomozygous108658704
1276283913276283914TC10GENIChomozygous108658705
1276284730276284731TC8GENIChomozygous108658706
1276285206276285207CA23GENIChomozygous108658707