chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120717884120717885GA7GENIChomozygous118417872
7120717939120717940CT5GENIChomozygous116081944
7120717980120717981AC13GENIChomozygous116081945
7120718002120718003AG15GENIChomozygous116081946
7120718603120718604TC12GENIChomozygous116081947
7120719496120719497GA4GENIChomozygous116262906
7120720857120720858GA25GENIChomozygous116081950
7120720954120720955GA28GENIChomozygous116409513
7120722609120722610CA25GENIChomozygous118417873
7120725358120725359AT16GENIChomozygous118259119
7120725618120725619CG22GENIChomozygous116081952
7120725712120725713CT24GENIChomozygous118417874
7120726101120726102CT21GENIChomozygous115856964
7120726240120726241CT29GENIChomozygous118417875
7120726286120726287CT27GENIChomozygous118417876
7120726485120726486TC20GENIChomozygous115856966
7120727329120727330TC20GENIChomozygous118417877
7120727634120727635CT31GENIChomozygous118417878
7120727943120727944CA33GENIChomozygous118417879
7120728267120728268AG27GENIChomozygous118417880
7120729017120729018GA22GENIChomozygous118417881
7120729148120729149CT14GENIChomozygous118417882
7120730401120730402GT21GENIChomozygous118417883
7120731659120731660GA21GENIChomozygous118417884
7120732091120732092TA17GENIChomozygous115856970
7120732771120732772GA26GENIChomozygous118417885
7120733282120733283TC18GENIChomozygous115856974
7120734151120734152CT26GENIChomozygous118417886
7120735584120735585AG26GENIChomozygous118417887
7120735686120735687CT25GENIChomozygous118417888
7120737618120737619TC18GENIChomozygous118417889
7120740892120740893CT10GENIChomozygous118512427
7120741692120741693CT18GENIChomozygous116409525
7120741962120741963TC21GENIChomozygous118417890
7120743750120743751TC5GENIChomozygous118512429
7120744208120744209CT28GENIChomozygous118417891