chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1190708927190708928AG45GENIChomozygous61022064
1190709870190709871TC40GENIChomozygous61022067
1190709917190709918TC34GENIChomozygous61022068
1190710229190710230TG51GENIChomozygous61917642
1190710882190710883GA47GENIChomozygous61022069
1190712029190712030TC47GENIChomozygous61022070
1190712147190712148AG55GENICpossibly homozygous61022071
1190712567190712568AG46GENICpossibly homozygous61022072
1190713092190713093A-2GENIChomozygous61022073
1190713849190713850TC43GENIChomozygous61022074
1190713960190713961AG46GENIChomozygous61917643
1190714268190714269A-45GENIChomozygous61022076
1190714685190714686TC35GENIChomozygous61917644
1190714954190714955AG47GENIChomozygous61022077
1190715632190715633GA49GENIChomozygous61917645
1190715945190715950TTTTC-----37GENIChomozygous61917646
1190715958190715960TT--29GENIChomozygous61022078
1190717083190717084TTA19GENICheterozygous61022080
1190717173190717174TC18GENICpossibly homozygous61022081
1190717187190717188A-3GENIChomozygous61917647
1190717397190717398GA28GENIChomozygous61572739
1190717411190717412AC23GENIChomozygous61022082
1190718341190718342TC55GENIChomozygous61022083
1190718930190718931TC47GENIChomozygous61022084
1190719107190719108CG50GENIChomozygous61022085
1190719484190719485CA40GENICpossibly homozygous61022086