chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4162815652162815653CT13GENIChomozygous58177726
4162816014162816015CCTGA7GENIChomozygous57005364
4162816122162816123CT7GENIChomozygous57005365
4162817573162817574CCTT33GENIChomozygous58177728
4162817677162817678GA15GENIChomozygous57005366
4162818245162818246T-3GENIChomozygous58177730
4162818305162818306TC8GENIChomozygous57005367
4162818985162818986CT13GENIChomozygous57005369
4162820400162820403TTT---11GENICheterozygous58351457
4162820401162820403TT--11GENICheterozygous58351459
4162821423162821424GA18GENIChomozygous58177732
4162822833162822834G-30GENIChomozygous57005372
4162823045162823046TC13GENIChomozygous58177734
4162823335162823336CT34GENIChomozygous58177736
4162823736162823738TT--7GENICheterozygous57005373
4162823916162823917AT14GENIChomozygous57005374
4162825448162825449TA14GENIChomozygous58177738
4162826305162826306TC23GENIChomozygous58177740
4162826977162826980TTA---13GENIChomozygous58177742
4162828157162828197TTGAATTCTTACTCTCTACCTGTCAGGATGCTGTTATACT----------------------------------------11GENIChomozygous58287873
4162828563162828564TC13GENIChomozygous57005378
4162828705162828706GGT8GENIChomozygous57005379
4162829144162829145GA18GENIChomozygous58177744
4162829492162829493AG14GENIChomozygous57005380
4162830068162830069A-10GENICheterozygous58351463
4162828482162828483TTAAAG14GENIChomozygous57844205