chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141763972417639725TC24GENIChomozygous950796947
141764052517640526TC13GENIChomozygous950796948
141764261817642619CT20GENIChomozygous950796949
141764265617642657CA17GENIChomozygous950796950
141764342217643423GC12GENIChomozygous950796951
141764352417643525CT13GENIChomozygous950796952
141764359417643595CA13GENIChomozygous950796953
141764416617644167GT28GENIChomozygous950796954
141764622417646225CT18GENIChomozygous950796955
141764869017648691GC18GENIChomozygous950796956
141765004317650044CT25GENIChomozygous950796957
141765031617650317TC17GENIChomozygous950796958
141765040117650402TC40GENIChomozygous950796959
141765048617650487CT19GENIChomozygous950796960
141765054617650547TC13GENIChomozygous950796961
141765054917650550CT12GENIChomozygous950796962
141765055317650554GA10GENIChomozygous950796963
141765061417650615CT8GENIChomozygous950796964
141765064217650643AT7GENIChomozygous950796965
141765064417650645AT7GENIChomozygous950796966
141765067217650673TG14GENIChomozygous950796967
141765072117650722AG19GENIChomozygous950796968
141765073017650731CT22GENIChomozygous950796969
141765115717651158AT17GENIChomozygous950796970
141765116317651164GA16GENIChomozygous950796971
141765141217651413AT17GENIChomozygous950796972
141765144717651448TG14GENIChomozygous950796973
141765161617651617AG12GENIChomozygous950796974
141765171817651719GA13GENIChomozygous950796975
141765172617651727GT12GENIChomozygous950796976
141765179617651797GA14GENIChomozygous950796977
141765416017654161GA13GENIChomozygous950796978
141765416217654163AG13GENIChomozygous950796979
141765581617655817TC24GENIChomozygous950796980
141765645617656457TC13GENIChomozygous950796981
141765649817656499CT18GENIChomozygous950796982
141765685017656851AG26GENIChomozygous950796983