chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1216946341694635GT22GENIChomozygous115577911
1216946481694650GC25GENIChomozygous128948639
1216947731694774C45GENIChomozygous128948640
1217147181714719A40GENIChomozygous128948656
1217147211714722A40GENIChomozygous128948657
1217165901716591AT34GENICpossibly homozygous115232434
1217147571714758GT27GENICpossibly homozygous118286903
1217118301711832AC38GENICheterozygous130405000
1217146941714694C43GENIChomozygous130405001
1217365851736585A44GENIChomozygous128948672
1217366471736648TA40GENIChomozygous115232500
1217366601736662AT39GENIChomozygous128948673
1217366751736675A38GENIChomozygous128948674
1217367221736723T42GENIChomozygous128948675
1217367531736753A39GENIChomozygous128948676
1217367881736789C42GENIChomozygous128948677
1217368301736831T40GENIChomozygous128948678
1217368361736837C40GENIChomozygous128948679
1217368721736873C40GENIChomozygous128948680
1217368901736891G42GENIChomozygous128948681
1217369221736923T38GENIChomozygous128948682
1217370201737021T34GENIChomozygous128948683
1217370501737051CA39GENIChomozygous115357111
1217370641737064G37GENIChomozygous128948684
1217370651737065C37GENIChomozygous128948685
1217370781737079T40GENIChomozygous128948686
1217370821737082C43GENIChomozygous128948687
1217371481737148A46GENIChomozygous128948688
1217791151779116GA47GENICheterozygous118234841
1217791401779141TC37GENICheterozygous123574355
1217791411779142GA37GENICheterozygous123574356
1217791441779145TG37GENICheterozygous123574357
1217791511779152AG36GENICheterozygous118334571
1217791521779153AG35GENICheterozygous123574358
1217791611779162CT35GENICheterozygous123574359
1217791621779163AT35GENICheterozygous118334572
1217791681779169AG35GENICheterozygous123574360
1217791691779170AG35GENICheterozygous130781780
1217791731779174CG34GENICheterozygous130781781
1217791741779175AG34GENICheterozygous130781782
1217794171779418AC56GENICheterozygous118234842
1217830061783007CT46GENICheterozygous133429171