chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1143402151143402152CT13GENIChomozygous928070001
1143403148143403149GA32GENIChomozygous928070002
1143403496143403497TG39GENIChomozygous928070003
1143403716143403717GA46GENIChomozygous928070004
1143404009143404010GA42GENIChomozygous928070005
1143404336143404337TG36GENIChomozygous928070006
1143405210143405211CT23GENIChomozygous928070007
1143408115143408116TA31GENIChomozygous928070008
1143413128143413129GA36GENIChomozygous928070009
1143413692143413693GA27GENIChomozygous928070010
1143414311143414312AT46GENIChomozygous928070011
1143414890143414891AG3GENIChomozygous928070012
1143414894143414895AG2GENIChomozygous928070013
1143416511143416512TG20GENIChomozygous928070014
1143417272143417273TC44GENIChomozygous928070015
1143417856143417857TC26GENIChomozygous928070016
1143418488143418489CT50GENIChomozygous928070017
1143419191143419192AC63GENIChomozygous928070018
1143419634143419635TC12GENIChomozygous928070019
1143420031143420032GT48GENIChomozygous928070020
1143421426143421427CG45GENIChomozygous928070021
1143421427143421428CT46GENIChomozygous928070022
1143423000143423001AG35GENIChomozygous928070023
1143423464143423465AG28GENIChomozygous928070024
1143423882143423883AG51GENIChomozygous928070025
1143423971143423972TG38GENIChomozygous928070026
1143424207143424208GC31GENIChomozygous928070027
1143424370143424371TA43GENIChomozygous928070028
1143424447143424448GA41GENIChomozygous928070029
1143424861143424862TA63GENIChomozygous928070030
1143425117143425118AG28GENIChomozygous928070031
1143425292143425293GT28GENIChomozygous928070032
1143425475143425476AG51GENIChomozygous928070033
1143425519143425520GA42GENIChomozygous928070034
1143426071143426072GA33GENIChomozygous928070035
1143426641143426642GA46GENIChomozygous928070036
1143426964143426965GA33GENIChomozygous928070037
1143427743143427744GA26GENIChomozygous928070038
1143429194143429195TC45GENIChomozygous928070039
1143429720143429721AG43GENIChomozygous928070040