chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13110139525110139528AGA---22GENIChomozygous49875466
13110139540110139541G-21GENIChomozygous49875468
13110139556110139557GA22GENIChomozygous49875470
13110143160110143161GGT9GENICheterozygous50536054
13110143162110143163T-9GENICheterozygous50554660
13110143576110143577AAG26GENIChomozygous49875471
13110154862110154863T-14GENIChomozygous49875475
13110154867110154868AG14GENIChomozygous49989080
13110154868110154869GT14GENIChomozygous49989081
13110154878110154879T-9GENIChomozygous49875476
13110154885110154886A-6GENIChomozygous49875478
13110154901110154902TTC3GENIChomozygous49875480
13110170062110170063CCTA9GENICheterozygous49989113
13110177416110177418GT--5GENICheterozygous50536060
13110178828110178830TA--2GENIChomozygous49875509
13110185598110185599GGCT3GENIChomozygous49875511
13110193299110193300CG33GENIChomozygous49875513
13110196382110196387GTCTC-----16GENICheterozygous50554667
13110196389110196395AAGGTA------18GENICheterozygous50554669
13110199196110199197GGAAAAA7GENICheterozygous50536062
13110200609110200611AC--5GENICheterozygous50536064
13110210762110210763CCA9GENIChomozygous49875516
13110214841110214843AC--5GENICheterozygous50536068
13110226999110227000TTAC6GENICheterozygous50587312
13110238332110238333TG9GENIChomozygous49875520
13110238338110238339TG10GENIChomozygous49875522
13110261931110261932AATTG29GENIChomozygous49875525
13110282875110282876AAAAAG16GENIChomozygous50603670
13110316109110316110C-4GENICheterozygous50554674
13110323537110323540AAT---22GENICheterozygous50603671
13110333194110333195G-7GENICheterozygous50566795